Job Description This Paramedic position performs duties within their scope of practice in an Emergency Room facility setting, under the direction of the on-duty provider. The Paramedic must have a current Paramedic Certification in the applicable state, with at least 1 year of Paramedic experience.Care for Emergency Department patientsPerformspatient care tasks under the direction of a providerCoordinatesthe plan of care for a group of assigned patients and consulting with other members of the health care team when indicated to ensure optimal patient outcomesDemonstratesproficiency and abides by policies, rules, guidelines, and procedures Job Requirements Applicable Experience:1 yearParamedic (KS) - Kansas Board of Emergency Medical Services Job Details Full TimeDay (United States of America) The best place to get care. The best place to give care . Saint Luke's 12,000 employees strive toward that vision every day. Our employees are proud to work for the only faith-based, nonprofit, locally owned health system in Kansas City. Joining Saint Luke's means joining a team of exceptional professionals who strive for excellence in patient care. Do the best work of your career within a highly diverse and inclusive workspace where all voices matter.Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer. Read Less

<p><strong>Description</strong></p> <p><strong>ASSISTED LIVING RN - Providence Elderplace Oregon - Irvington Village Portland, OR</strong></p> <p><strong>Schedule:</strong> Full time, Day Shift</p> <p><strong>Location:</strong> Irvington Village Residential Care Facility Portland, OR only</p> <p><strong>Job description:</strong></p> <p>The RN Housing Care Manager oversees and coordinates the care and services for at-risk frail elder patients with complex medical and psychosocial needs. The RN Housing Care Manager provides professional nursing care for residents of ElderPlace program housing. Care is consistent with the Oregon Nurse Practice Act and Oregon Administrative Rules and Regulations for Assisted Living and Residential Care Facilities. The RN applies knowledge based on the nursing process while performing assessments and evaluating for changes of condition. The goal of the RN Housing Care Manager is to provide care that is appropriate and personalized.</p> <p>Providence PACE is a Program of All-Inclusive Care for the Elderly that strives to keep older adults as healthy as possible living in the community through clinics, home visits and more. Join our team to help empower elders in your community to live active, independent lives.</p> <p><strong>Benefits and perks:</strong></p> <ul><li>Competitive pay (including holiday pay & shift pay differentials)</li> <li>Best-in-class benefits – full medical, dental and vision coverage from your first day</li> <li>401(k) plan with employer matching & complementary retirement planner</li> <li>Generous paid time off for vacation, sick days and holidays</li> <li>Mileage reimbursement for roles traveling to patient homes</li> <li>Tuition reimbursement & student loan forgiveness programs</li> <li>Wellness & mental health assistance programs</li> <li>Back-up child & elder care to help with care disruptions for your family</li> <li>Voluntary benefits, like pet, auto and home insurance, and more!</li> </ul><p><strong>Required Qualifications:</strong></p> <ul><li>Coursework/Training: Relevant training applicable to the position, as specified by the Nurse Manager.</li> <li>Upon hire: Oregon Registered Nurse License</li> <li>Within 30 days of hire: National Provider BLS - American Heart Association</li> <li>Upon hire: Relevant certifications applicable to the position, as specified by the Nurse Manager</li> <li>Upon hire: In compliance with company policy and state regulations, a Department of Human Services (DHS) criminal background check may be required based upon the location of the position. Fingerprinting may be required also. (for ElderPlace)</li> <li>1 year ElderPlace</li> <li>Experienced within Specialty: RN experience in a PACE organization.</li> </ul><p><strong>Preferred Qualifications:</strong></p> <ul><li>Bachelor's Degree: Nursing</li> <li>1 year Acute care RN experience.</li> <li>2 years ElderPlace</li> <li>New to Specialty: RN experience in Residential Care / Assisted Living or Community-Based care.</li> </ul><p><strong>Why Join Providence?</strong></p> <p>Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.</p> <p>Accepting a new position at another facility that is part of the Providence family of organizations may change your current benefits. Changes in benefits, including paid time-off, happen for various reasons. These reasons can include changes of Legal Employer, FTE, Union, location, time-off plan policies, availability of health and welfare benefit plan offerings, and other various reasons.</p> <p><strong>About Providence</strong></p> <p>At Providence, our strength lies in Our Promise of “Know me, care for me, ease my way.” Working at our family of organizations means that regardless of your role, we’ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable.</p> <p>The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</p> <p>Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.</p> <p><strong>About the Team</strong></p> <p>Providence Home and Community Care (HCC) is a service line within Providence with over 8,000 caregivers and 2,000 volunteers serving nearly 200,000 people a year, in their homes, in clinics and in a variety of congregate living ministries across our seven-state footprint.</p> <p>HCC provides a full range of services and support for people of all ages, especially those facing chronic or life-limiting illnesses. Our core competencies include restorative care, longitudinal care and care through the end of life. Our service lines include assisted living/skilled nursing/rehabilitation, home health, home infusion/pharmacy services, home medical equipment, hospice and palliative care, Program of All-Inclusive Care for the Elderly (PACE), personal home services/private duty care and supportive housing.</p> <p>Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.</p> <p> <strong>Requsition ID:</strong> 369771 </p><p><strong>Company:</strong> Providence Jobs </p><p><strong>Job Category:</strong> Patient Care (Non-Acute) </p><p><strong>Job Function:</strong> Clinical Care </p><p><strong>Job Schedule:</strong> Full time </p><p><strong>Job Shift:</strong> Day </p><p><strong>Career Track:</strong> Nursing </p><p><strong>Department:</strong> 5014 ASSISTED LIVING OR PORTLAND IRVINGTON VILLAGE </p><p><strong>Address:</strong> OR Portland 420 NE Mason </p><p><strong>Work Location:</strong> Elderplace Irvington Village-Portland </p><p><strong>Workplace Type:</strong> On-site </p><p><strong>Pay Range:</strong> $41.37 - $64.23 </p><p>The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</p><p><script id="detrack" defer src="https://d2e48ltfsb5exy.cloudfront.net/p/t.js?i=0,1" data-g="DA9B3ADFADB0459AA86EF037804F13D05521"></script></p>PandoLogic. Category: , Keywords: Assisted Living Nurse Read Less

<p><strong>Description</strong></p> <p><strong>Clinical Program Coordinator RN at Providence Seaside Hospital is 1.0 FTE full time position working during weekdays on a day shift.</strong></p> <p>The Coordinator supports the provision and quality of nursing services at the facility level through coordination of activities within a defined focus that support of Providence Health & Services System and Regional goals. This includes assuring a balance of optimal and efficient patient care; staff, patient, and physician satisfaction; and cooperative partnerships with other organizational departments and professional groups. With a constant focus on patient-centeredness, and staff and patient safety, the Coordinator supports standards and systems for care delivery for their facility. These systems of care delivery promote evidence-based practice and are designed to support the management of productivity targets within a context of constant change in patient volumes, patient acuity, and available resources.</p> <p>Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence Seaside Hospital and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.</p> <p><strong>Required Qualifications:</strong></p> <ul><li>Bachelor's Degree in Nursing.</li> <li>Upon hire: Oregon Registered Nurse License.</li> <li>Upon hire: National Provider BLS - American Heart Association.</li> <li>6 years Nursing with experience in progressive leadership roles.</li> <li>5 years of Clinical experience in cardiac ambulatory and/or cardiac interventions.</li> </ul><p><strong>Preferred Qualifications:</strong></p> <ul><li>Master's Degree in Nursing or related field.</li> </ul><p><strong>Why Join Providence?</strong></p> <p>Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.</p> <p><strong>About Providence</strong></p> <p>At Providence, our strength lies in Our Promise of “Know me, care for me, ease my way.” Working at our family of organizations means that regardless of your role, we’ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable.</p> <p>The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</p> <p>Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.</p> <p><strong>About the Team</strong></p> <p>Providence has been serving the Pacific Northwest since 1856 when Mother Joseph of the Sacred Heart and four other Sisters of Providence arrived in Vancouver, Washington Territory. As the largest healthcare system and largest private employer in Oregon, Providence is located in areas ranging from the Columbia Gorge to the wine country to sunny southern Oregon to charming coastal communities to the urban setting of Portland.</p> <p>Our award-winning and comprehensive medical centers are known for outstanding programs in cancer, cardiology, neurosciences, orthopedics, women's services, emergency and trauma care, pediatrics and neonatal intensive care. Our not-for-profit network also provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care.</p> <p>Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.</p> <p> <strong>Requsition ID:</strong> 372323 </p><p><strong>Company:</strong> Providence Jobs </p><p><strong>Job Category:</strong> Clinical Administration </p><p><strong>Job Function:</strong> Clinical Support </p><p><strong>Job Schedule:</strong> Full time </p><p><strong>Job Shift:</strong> Day </p><p><strong>Career Track:</strong> Nursing </p><p><strong>Department:</strong> 5000 PSH SURGERY </p><p><strong>Address:</strong> OR Seaside 725 S Wahanna Rd </p><p><strong>Work Location:</strong> Providence Seaside Hospital-Seaside </p><p><strong>Workplace Type:</strong> On-site </p><p><strong>Pay Range:</strong> $45.99 - $71.40 </p><p>The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.</p><p><script id="detrack" defer src="https://d2e48ltfsb5exy.cloudfront.net/p/t.js?i=0,1" data-g="86E1EE77DEB642A79C37074C2BDE46805521"></script></p>PandoLogic. Category: , Keywords: Healthcare Program Coordinator Read Less

Job Description SummaryThis position will be located at Durham, NC site and will not have the ability to be located remotely. Job Title: QC AnalystSummary:The Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.We are recruiting for both day shift and night shift. The hours are as follows:Day shift: 8:00 AM - 4:00 PM / 9:00 AM - 5:00 PMNight shift: 3:00 PM - 1:40 AM #LI-OnsiteKey Responsibilities:• Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to cell-based methods (potency, AA), PCR (ddPCR, qPCR), Immunoassays (ELISA), chromatography (HPLC-UV), AUC, compendial assays (Bioburden, pH), electrophoresis (CE, Western Blot), cell culturing, and Microbiology/Release sampling (EM, Compressed Gas). • Responsible for limited range of laboratory support functions and procedures as assigned, developing capability in basic technical skills, disciplines, and procedures within assigned discipline area(s). • May be assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing operating procedures. • Capable of delivering to assigned work schedule with attention to detail and accuracy. • Notifies management and initiates events (such as Laboratory Investigations) in the quality systems, with guidance from senior analysts or management. • Assist in special projects on analytical and instrument problem solving by execution of assay. • Gain familiarity with basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. • Other related job duties as assigned. Job DescriptionRequirements: Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Ability to communicate and work in a team environment. Normally receives detailed instructions on all work. Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $27.40/hr - $51.58/hr ; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.Company will not sponsor visas for this position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$57,800.00 - $107,300.00 Skills DesiredContinued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence Read Less

Job Description SummaryThe Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.Location: Durham, NC #LI-Onsite Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to ddPCR, ELISAs, NGS and Western Blot.Assists in the evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards.Reviews data obtained for compliance to specifications and reports abnormalities. Performs trend analysis of methods/environmental data/assay controls & standards and draws conclusions.Capable of delivering to assigned work schedule with attention to detail and accuracy.Support department risk assessments and participates in audit walk-throughs.Participates in the preparation of investigations, summaries and reports.Reviews data obtained for compliance to specifications and reportsInvestigates and resolves non-conforming test results by completing thorough Deviation, OOS/OOT/OOE and Investigation.Authors new/revise Standard Operating Procedures, Protocols / Summary Reports /Analytical Master Plans for QC.Oversees special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines.Supports training of departmental personnel in appropriate technique and related topics.Essential Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field requiredFor Specialist:  5 years’ experience in GMP environment or 4 years within Novartis Gene TherapiesFor Senior Specialist:  8 years’ experience in GMP environment or 7 years within Novartis Gene Therapies.Excellent interpersonal, verbal and written communication skills with strong technical writing experience required. Previous investigation experience a plus.Proven ability to work effectively in a team environment. Collaborates cross functionally with other departments to achieve site goals.Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action including critically thinking, troubleshooting and problem-solving skills.Normally receives general instructions on routine work, detailed instructions on new projects or assignments.Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties.The salary for this position is expected to range between $29.13/hr and $54.13/hr.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.Company will not provide visa sponsorship for this position.  Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.   EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$60,600.00 - $112,600.00 Skills DesiredContinued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management Read Less

Job Description SummaryThis position will be located at Durham, NC site and will not have the ability to be located remotely. Job Title: QC AnalystSummary:The Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.We are recruiting for both day shift and night shift. The hours are as follows:Day shift: 8:00 AM - 4:00 PM / 9:00 AM - 5:00 PMNight shift: 3:00 PM - 1:40 AM #LI-OnsiteKey Responsibilities:• Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to cell-based methods (potency, AA), PCR (ddPCR, qPCR), Immunoassays (ELISA), chromatography (HPLC-UV), AUC, compendial assays (Bioburden, pH), electrophoresis (CE, Western Blot), cell culturing, and Microbiology/Release sampling (EM, Compressed Gas). • Responsible for limited range of laboratory support functions and procedures as assigned, developing capability in basic technical skills, disciplines, and procedures within assigned discipline area(s). • May be assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing operating procedures. • Capable of delivering to assigned work schedule with attention to detail and accuracy. • Notifies management and initiates events (such as Laboratory Investigations) in the quality systems, with guidance from senior analysts or management. • Assist in special projects on analytical and instrument problem solving by execution of assay. • Gain familiarity with basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. • Other related job duties as assigned. Job DescriptionRequirements: Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Ability to communicate and work in a team environment. Normally receives detailed instructions on all work. Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $27.40/hr - $51.58/hr ; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.Company will not sponsor visas for this position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$57,800.00 - $107,300.00 Skills DesiredContinued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence Read Less

Job Description Summary#LI-OnsiteThis role is located onsite in Durham, NC. As Site Engineering Head, you’ll be at the forefront of shaping the future of our Durham site. This is your opportunity to lead a high-performing team and drive strategic engineering initiatives that directly impact production success, compliance, and innovation. From lifecycle management to capital investments, your leadership will ensure our facilities and systems are not only operationally excellent but also aligned with global standards and future-ready. If you are dedicated to engineering excellence, skilled in people leadership, and aspire to make a significant impact in a dynamic, science-driven environment—this is your opportunity. Job DescriptionKey Responsibilities:Lead site-wide engineering, maintenance, and facility strategies to support production and operational excellenceInfluences and participates in the site leadership team, establishing effective cross-functional leadership relationships and presenceOversee lifecycle management of equipment, utilities, and facilities from selection to compliant operationDevelop and maintain a 5-year Master Plan and annual capital investment roadmapExecute capital and operational projects on time and within budget to support site goalsPartner with ITOT (Information Technology & Operational Technology) to resolve automation issues and support engineering initiativesEnsure audit readiness and compliance with all Quality and EHS regulationsManage engineering budgets, resources, and performance metrics effectivelyDrive continuous improvement using Operational Excellence and best practice frameworksBuild and lead a high-performing team of internal and contract engineering professionalsEssential Requirements:Bachelor’s degree in Engineering or a related disciplineMinimum 15 years of experience in a pharmaceutical or biopharmaceutical environmentProven leadership in building and guiding high-performing technical teamsStrong knowledge of validation, automation, and manufacturing systems and technologiesDemonstrated ability to manage capital and operational budgets effectivelyExperience representing engineering systems in regulatory audits and inspectionsWorking knowledge of facility and utility systems, including process controls and engineering practicesUnderstanding of environmental, health, and safety (EHS) standards and compliance expectations5-10% travelDesirable Requirements:Master’s degree in Engineering or related field preferredFamiliarity with biotechnology platforms, aseptic processing, and current pharmaceutical technology trends preferredNovartis Compensation and Benefit Summary:The salary for this position is expected to range between $132,300 and $245,700 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.Company will not sponsor visas for this position.  EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$132,300.00 - $245,700.00 Skills DesiredAutomation, Capital Expenditure, Change Management, Classification Systems, Critical Thinking, Efficiency, Flexibility, General Hse Knowledge  , Including Gdp, Knowledge Of Gmp, Manufacturing Process (Production), Operations, Root Cause Analysis (RCA), Support Services Read Less

Job Description SummaryThe Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.Location: Durham, NC #LI-Onsite Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to chromatography (HPLC-UV), AUC, compendial assays (pH, Conductivity), electrophoresis (CE, Western Blot), and Release sampling (EM, Compressed Gas).  Responsible for limited range of laboratory support functions and procedures as assigned, developing capability in basic technical skills, disciplines, and procedures within assigned discipline area(s). May be assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing operating procedures. Capable of delivering to assigned work schedule with attention to detail and accuracy. Notifies management and initiates events (such as Laboratory Investigations) in the quality systems, with guidance from senior analysts or management. Assist in special projects on analytical and instrument problem solving by execution of assay. Gain familiarity with basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. Key Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Ability to communicate and work in a team environment. Normally receives detailed instructions on all work.The salary for this position is expected to range between $26.44/hr and $49.13/hr.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$55,000.00 - $102,200.00 Skills DesiredAgility, Audit Management, Business Partnering, Continued Learning, Health Authorities, Influencing Skills, Knowledge Of Capa, Quality Management, Risk Management, Root Cause Analysis (RCA), Self-Awareness, Sop (Standard Operating Procedure), Technological Expertise Read Less

Job Description SummaryThe Senior Analyst, Quality Control, Cell-based methods will support activities within the Quality Control department, with a focus on cell-based methods such as Adventitious Agents, rcAAV, potency, etc. This role will utilize laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), QC Methods & current Compendia. This role is based 100% on-site.Location: Durhan, NC #LI-OnsiteShift: 1st. Some night and weekend work may be required Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to cell-based methods (potency, AA), PCR (ddPCR, qPCR), Immunoassays (ELISA), chromatography (HPLC-UV, HPLC-ELSD, HPLC-MS), AUC, compendial assays (Bioburden, pH) and electrophoresis (CE, Western Blot).  Ensures assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing and authors new operating procedures. Capable of delivering to assigned work schedule with attention to detail and accuracy. Notifies management, initiates (such as Laboratory Investigations) and authors minor events/discrepancies in the quality systems, with little to no guidance from advisor or management. Understands the basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. May facilitate training to other team members in the organization. Ensures calibrates and maintains lab and analytical equipment are performed within established period. Conducts review of logbooks and may perform reviews as assigned by management May assist in drafting technical documents such as Protocols / Report to support method verification/validations. Other related job duties as assigned Essential Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field with 2 years’ experience in GMP environment. Developing professional expertise, applies company policies and procedures to resolve a variety of issues.  Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.   Exercises judgment within defined procedures and practices to determine appropriate action including the critically thinking, troubleshooting and problem-solving skills.Normally receives general instructions on routine work, detailed instructions on new projects or assignments. Excellent interpersonal, verbal and written communication skills with strong technical writing experience required and ability to work in a team environment. Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties. Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $32.12/hour and $59.62/hour; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.  EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$66,800.00 - $124,000.00 Skills DesiredAgility, Audit Management, Business Partnering, Continued Learning, Health Authorities, Influencing Skills, Knowledge Of Capa, Quality Management, Risk Management, Root Cause Analysis (RCA), Self-Awareness, Sop (Standard Operating Procedure), Technological Expertise Read Less

Job Description SummaryThis position will be located at Durham, NC and will not have the ability to be located remotely.The BioProcess Engineer downstream/Fill-Finish is responsible for executing the manufacturing operations at the plant/site. The level of the role will be determined by the years of relevant experience. #LI-OnsiteKey Responsibilities: This role is a 2-2-3 day shift position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. • Performs commercial and clinical manufacturing operations on the site, including purification (downstream), fill-finish (drug product, visual inspection, packaging), media/buffer preparation, and any additional supporting activities. • Learns to troubleshoot equipment, participates in interviews on deviations, partners with other business units to assist in manufacturing led deviations, standardizes equipment, and cleans production area.• Assists in determining root cause, implementing solutions and verifying solutions are effective.• Assists with the creation and on-going maintenance of all pertinent equipment, policies, and procedures.• Learn and perform aseptic techniques applicable to cell culture, recovery, purification, aseptic fill/finish (upstream and downstream).• Supports the product requirements to ensure that all products are produced according to plan. Learn cGMP and cGDP and ensure cGMP documentation is being filled out correctly, training is current, and all quality requirements are being followed.• Maintains quality standards to meet cGMP requirements, CFR’s, and internal company policies directly related to the manufacturing process.• Partners with the Quality department to ensure a compliant manufacturing environment. Job DescriptionDesirable Requirements: For BioProcess Engineer I - Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field or 2 years equivalent experience;For for BioProcess Engineer II - Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field and 2 years’ experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment; OR four (4) years’ experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment in lieu of degree;For BioProcess Engineer III - Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field and 4 years’ experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment; OR six (6) years’ experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment in lieu of degreeExcellent oral and written communication skillsEntry level into the biopharmaceutical based GMP manufacturing operations, no experience necessary.Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted. Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $66,800 and $124,000/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.Company will not sponsor visas for this position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$66,800.00 - $124,000.00 Skills DesiredAssembly Language, Cooperation, Efficiency, Electronic Components, Flexibility, General Hse Knowledge  , Good Documentation Practice, Installations (Computer Programs), Iso (International Organization For Standardization), Job Description, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Nuclear Medicine, Physics, Product Distribution, Production Line, Scheduler Read Less

Job Description Summary#LI-OnsiteLocation: This role is located on-site in Durham, NC.The Project Director, Drug Product is responsible for managing the project at an operational level. This includes ensuring the project meets its objectives regarding operational functionality, Quality & HSE compliance, and adherence to regulations within the approved scope, budget, and timeline. The role involves overseeing a significant capital investment and start-up facility. Additionally, the Project Director must supervise the aseptic filling and packaging processes, ensuring that these procedures are carried out in sterile environments to maintain product integrity and safety. Job DescriptionRole responsibilities:Leads the senior project team and serves as the primary point of contact for project governance. Accountable for project team performance and developing a comprehensive project plan.Aligns project strategy and deliverables with key business stakeholders.Responsible for budget management, unit cost control, and financial KPIs.Manages the project budget, schedule, and quality requirements.Conducts risk management and develops contingency plans.Leading large capital project execution from design through commercialization.Managing sterile processing, filling, and packaging operations.Develops a robust organizational structure and resource strategy to smoothly transition from project phase to commercial operations. Provides coaching and mentoring, promoting an inclusive and high-performance culture.Ensures regulatory compliance readiness for inspections and audits.Maintains acceptable standards of product/process quality, HSE, and Security.Role Requirements:Bachelor’s degree in Life Sciences, Chemistry, Pharmacy, or Engineering; Advanced degree preferred.Minimum 10 years of experience in senior Manufacturing, Technical Operations and Supply Chain Management roles in the pharmaceutical or life sciences industry.Demonstrated experience in leadership and change management, along with prior success in developing and overseeing multi-level organizations within aseptic manufacturing.Possesses the ability to work in a global, networked environment.Demonstrated expertise in developing and managing site organizations, spanning from large-scale capital project design and construction to commercialization phases.Desirable Requirements: Experience in drug product within large molecule preferred.Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $160,300 to $297,700/yearly. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$160,300.00 - $297,700.00 Skills DesiredAssembly Language, Biotechnology, Change Management, Chemistry, Continual Improvement Process, Cost Reduction, Finance, General Hse Knowledge     , Incentive Program, Installations (Computer Programs), Knowledge Of Gmp, Leadership, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Operational Excellence, Productivity, Purchase, Six Sigma Read Less

Job Description Summary#LI-OnsiteThis role is located onsite in Durham, NC. As Site Engineering Head, you’ll be at the forefront of shaping the future of our Durham site. This is your opportunity to lead a high-performing team and drive strategic engineering initiatives that directly impact production success, compliance, and innovation. From lifecycle management to capital investments, your leadership will ensure our facilities and systems are not only operationally excellent but also aligned with global standards and future-ready. If you are dedicated to engineering excellence, skilled in people leadership, and aspire to make a significant impact in a dynamic, science-driven environment—this is your opportunity. Job DescriptionKey Responsibilities:Lead site-wide engineering, maintenance, and facility strategies to support production and operational excellenceInfluences and participates in the site leadership team, establishing effective cross-functional leadership relationships and presenceOversee lifecycle management of equipment, utilities, and facilities from selection to compliant operationDevelop and maintain a 5-year Master Plan and annual capital investment roadmapExecute capital and operational projects on time and within budget to support site goalsPartner with ITOT (Information Technology & Operational Technology) to resolve automation issues and support engineering initiativesEnsure audit readiness and compliance with all Quality and EHS regulationsManage engineering budgets, resources, and performance metrics effectivelyDrive continuous improvement using Operational Excellence and best practice frameworksBuild and lead a high-performing team of internal and contract engineering professionalsEssential Requirements:Bachelor’s degree in Engineering or a related disciplineMinimum 15 years of experience in a pharmaceutical or biopharmaceutical environmentProven leadership in building and guiding high-performing technical teamsStrong knowledge of validation, automation, and manufacturing systems and technologiesDemonstrated ability to manage capital and operational budgets effectivelyExperience representing engineering systems in regulatory audits and inspectionsWorking knowledge of facility and utility systems, including process controls and engineering practicesUnderstanding of environmental, health, and safety (EHS) standards and compliance expectations5-10% travelDesirable Requirements:Master’s degree in Engineering or related field preferredFamiliarity with biotechnology platforms, aseptic processing, and current pharmaceutical technology trends preferredNovartis Compensation and Benefit Summary:The salary for this position is expected to range between $132,300 and $245,700 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.Company will not sponsor visas for this position.  EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$132,300.00 - $245,700.00 Skills DesiredAutomation, Capital Expenditure, Change Management, Classification Systems, Critical Thinking, Efficiency, Flexibility, General Hse Knowledge  , Including Gdp, Knowledge Of Gmp, Manufacturing Process (Production), Operations, Root Cause Analysis (RCA), Support Services Read Less

Job Description SummaryThe Senior Specialist, Quality Assurance Compliance supports the implementation of robust Quality Systems for the Durham Site of Novartis Gene Therapies, considering global regulatory and local requirements of the organization. This role contributes significantly to the execution of these systems, authors or contributes to the procedures governing these systems and works towards timely implementation, including support of Quality Management Review, ownership/execution of Self‐Inspection program and in the management of health authority inspections.Location: Durham, NC #LI-Onsite, Hybrid Job DescriptionKey Responsibilities: Contributes significantly to the Readiness Program; site inspection preparation, program management, response and commitment process for health authority inspections.Leads site self-inspection program including preparation of risk based annual audit plan, lead auditor responsibilities, audit agendas, inspection reports and CAPA plan approvals.Provide strategic quality input on the design and architecture of Novartis Gene Therapies Quality Management System.Supports the development and oversight of robust quality systems, including both implementation and operation at site level.Supports management to implement and maintain the following programs: Annual Product Quality Review (APQR), Compliance Alert actions, and Novartis Global document assessments required to be performed at the site level.Supports supplier monitoring and oversite activities including audit responses, CAPAs, and evaluation of supplier risk levels.Supports the site level Quality Management Review (QMR) program including monitoring and reporting key performance indicators, as appropriate.Performs duties as assigned to ensure compliance with global and local regulations.Represent Quality Assurance Compliance team on project teams and in meetings as needed.Support the continuous improvement and oversight of QA Compliance programs through planning and implementation.Identifies and implements new technologies to improve compliance an efficiency of QS operations.Adheres to all GMP requirements.Ownership of Compliance Records relevant to quality systems responsibilities (Change Records, CAPAs, Quality Events, Deviations as needed).Essential Requirements: Bachelor’s degree in Life Sciences or Chemistry (preferred) or related relevant degree with 7 years of experience in GMP manufacturing operations, Bio-Pharma or Gene therapies preferred.Previous experience in QA Compliance including self‐inspections, health authority inspections and supplier auditing, preferably with a minimum of 2 year’s of experience as a lead inspector.Experience reviewing systems and analyze data (paper or electronic) to identify specific compliance and data consistency issues.Previous Quality Assurance experience required, including Data Integrity (ALCOA+) compliance.            Ability to apply a phase appropriate, risk‐based approach to QA operational decisions.Experience supporting cGMP manufacturing operations through administration and enforcement of the Quality Management System.Proficient in cGMP/ICH/FDA/EU regulations and guidelines and experience in US and international regulatory agency inspections a plus.Proficient in using Microsoft applications (MS Word, MS Excel, MS PowerPoint).Strong follow‐up and organizational skills and ability to manage cross functional projects.Experience with viral gene therapies and/or orphan disease indications a plus.Direct experience reviewing and/or authoring standard operating procedures.Ability to work well independently and within a team.Excellent oral and written communication skills with technical writing experience required.The salary for this position is expected to range between $73,500 and $136,500 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$73,500.00 - $136,500.00 Skills DesiredContinued Learning, Gmp Procedures, Managing Ambiguity, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technical Knowledge, Technological Intelligence Read Less

Job Description SummaryPosition: Senior/Level III Engineer, AutomationThis position will be located at Durham, NC and will not have the ability to be located remotely.The Senior Automation Engineer reports to the AD Process Automation and is responsible for providing automation design team leadership and serving as a technical subject matter expert for a Novartis gene therapy manufacturing facility. This includes responsibilities for maintaining, troubleshooting, and modifying the GMP and non-GMP control systems. Systems include plant wide DCS (DeltaV), BMS (Rockwell SCADA) and 3rd party local control systems.#LI-OnsiteKey Responsibilities: • Provide design, configuration, installation, and maintenance of automation software and associated hardware; including interacting with other teams as necessary.• Provide oversight or participation on automation aspects of future projects including integration of 3rd party equipment to the plant DCS and BMS systems, data concentration, batch reporting, and data retention.• Prepare scopes of work for large projects and manage automation contractors as required to complete required work within project timelines.• Develop project objectives working with user requirements and business plans.• Determine equipment or system specifications and most cost-effective technology to be implemented.• Lead discussions with internal business partners on priorities, timelines and transparent sharing of information.• Establish equipment specifications in standard documentation – User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS/HDS/SDS).• Take programs from concept thru execution while managing all stages in the process utilizing a strong set of project management tools.• Maintain procedures to meet GMP requirements, CFR’s and internal company policies.• Participate and/or lead new product implementation processes to ensure smooth transition from process development into GMP manufacturing. Job DescriptionThe level of the position will be commensurate with education, applicable experience, competency and  independence. Senior Engineer AutomationB.S. degree in Engineering, Computer Science, or related technical field.8 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (12 years) in pharmaceutical or biopharmaceutical based GMP manufacturing operations.Excellent oral and written communication skills, including demonstrated technical writing skills.Experience programming, troubleshooting, and maintaining site DCS systems, preferably DeltaV.Experience programming, troubleshooting, and maintaining site SCADA/HMI systems, preferably Rockwell FactoryTalk View SE.Experience programming, troubleshooting, and maintaining site PLC/BMS systems, preferably Allen Bradley CompacLogix/ControlLogix.Experience programming, troubleshooting, and maintaining site data historian, preferably OSI PI.Level III Engineer AutomationB.S. degree in Engineering, Computer Science, or related technical field.5 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (9 years) in pharmaceutical or biopharmaceutical based GMP manufacturing operations.Excellent oral and written communication skills.Experience programming, troubleshooting, and maintaining site DCS systems, preferably DeltaV.Experience programming, troubleshooting, and maintaining site SCADA/HMI systems, preferably Rockwell FactoryTalk View SE.Experience programming, troubleshooting, and maintaining site PLC/BMS systems, preferably Allen Bradley CompacLogix/ControlLogix.Experience programming, troubleshooting, and maintaining site data historian, preferably OSI PI.Experience in system level validation testingNovartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $103,600 and $192,400/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.Company will not sponsor visas for this position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$103,600.00 - $192,400.00 Skills DesiredApi (Application Programming Interface), Api (Application Programming Interface), Automation Technology, Back-End Development, Business Continuity, Change Controls, Chemistry, Design Development, Electronic Components, General Hse Knowledge  , Including Gdp, Java, Knowledge Of Capa, Knowledge Of Gmp, Kubernetes, Managing Performance Improvement, Manufacturing Production, Mathematical Optimization, Project Commissioning, Project Engineering, Project Implementations, React.js, Risk Management, Root Cause Analysis (RCA), Scrum (Programming Methodology) {+ 2 more} Read Less

Job Description Summary#LI-OnsiteLocation: This role is located on-site in Durham, NC.The Project Director, Drug Substance within Large Molecule, is responsible for regulatory compliance, strategic leadership, and operational management. This position involves managing technical complexity, process scale-up, regulatory requirements, and cross-functional coordination. The role includes overseeing a significant capital investment and start-up facility. By applying scientific expertise alongside leadership and problem-solving skills, the Project Director ensures the quality production of drug substances for large-molecule therapies. Job DescriptionRole responsibilities:Leads the senior project team and serves as the primary point of contact for project governance. Accountable for project team performance and developing a comprehensive project plan.Aligns project strategy and deliverables with key business stakeholders.Responsible for budget management, unit cost control, and financial KPIs.Manages the project budget, schedule, and quality requirements.Conducts risk management and develops contingency plans.Leads capital project execution from design through commercialization.Instrumental in leading Tech Transfer and scale-up activitiesDevelops a robust organizational structure and resource strategy to smoothly transition from project phase to commercial operations. Provides coaching and mentoring, promoting an inclusive and high-performance culture.Ensures regulatory compliance readiness for inspections and audits.Maintains acceptable standards of product/process quality, HSE, and Security.Role Requirements:Bachelor’s degree in Life Sciences, Chemistry, Pharmacy, or Engineering; Advanced degree preferred.Minimum 10 years of experience in senior Manufacturing, Technical Operations and Supply Chain Management roles in the pharmaceutical or life sciences industry.Demonstrated experience in leadership and change management, along with prior success in developing and overseeing multi-level organizations.Possesses the ability to work in a global, networked environment.Demonstrated expertise in developing and managing site organizations, spanning from large-scale capital project design and construction to commercialization phases.Desirable Requirements: Experience in drug substance within large molecule preferred.Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $160,300 to $297,700/yearly. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$160,300.00 - $297,700.00 Skills DesiredAssembly Language, Biotechnology, Change Management, Chemistry, Continual Improvement Process, Cost Reduction, Finance, General Hse Knowledge     , Incentive Program, Installations (Computer Programs), Knowledge Of Gmp, Leadership, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Operational Excellence, Productivity, Purchase, Six Sigma Read Less

Job Description SummaryThe Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.Location: Durham, NC #LI-Onsite Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to chromatography (HPLC-UV), AUC, compendial assays (pH, Conductivity), electrophoresis (CE, Western Blot), and Release sampling (EM, Compressed Gas).  Responsible for limited range of laboratory support functions and procedures as assigned, developing capability in basic technical skills, disciplines, and procedures within assigned discipline area(s). May be assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing operating procedures. Capable of delivering to assigned work schedule with attention to detail and accuracy. Notifies management and initiates events (such as Laboratory Investigations) in the quality systems, with guidance from senior analysts or management. Assist in special projects on analytical and instrument problem solving by execution of assay. Gain familiarity with basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. Key Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Ability to communicate and work in a team environment. Normally receives detailed instructions on all work.The salary for this position is expected to range between $26.44/hr and $49.13/hr.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$55,000.00 - $102,200.00 Skills DesiredAgility, Audit Management, Business Partnering, Continued Learning, Health Authorities, Influencing Skills, Knowledge Of Capa, Quality Management, Risk Management, Root Cause Analysis (RCA), Self-Awareness, Sop (Standard Operating Procedure), Technological Expertise Read Less

Job Description SummaryThe Senior Specialist, Quality Assurance Compliance supports the implementation of robust Quality Systems for the Durham Site of Novartis Gene Therapies, considering global regulatory and local requirements of the organization. This role contributes significantly to the execution of these systems, authors or contributes to the procedures governing these systems and works towards timely implementation, including support of Quality Management Review, ownership/execution of Self‐Inspection program and in the management of health authority inspections.Location: Durham, NC #LI-Onsite, Hybrid Job DescriptionKey Responsibilities: Contributes significantly to the Readiness Program; site inspection preparation, program management, response and commitment process for health authority inspections.Leads site self-inspection program including preparation of risk based annual audit plan, lead auditor responsibilities, audit agendas, inspection reports and CAPA plan approvals.Provide strategic quality input on the design and architecture of Novartis Gene Therapies Quality Management System.Supports the development and oversight of robust quality systems, including both implementation and operation at site level.Supports management to implement and maintain the following programs: Annual Product Quality Review (APQR), Compliance Alert actions, and Novartis Global document assessments required to be performed at the site level.Supports supplier monitoring and oversite activities including audit responses, CAPAs, and evaluation of supplier risk levels.Supports the site level Quality Management Review (QMR) program including monitoring and reporting key performance indicators, as appropriate.Performs duties as assigned to ensure compliance with global and local regulations.Represent Quality Assurance Compliance team on project teams and in meetings as needed.Support the continuous improvement and oversight of QA Compliance programs through planning and implementation.Identifies and implements new technologies to improve compliance an efficiency of QS operations.Adheres to all GMP requirements.Ownership of Compliance Records relevant to quality systems responsibilities (Change Records, CAPAs, Quality Events, Deviations as needed).Essential Requirements: Bachelor’s degree in Life Sciences or Chemistry (preferred) or related relevant degree with 7 years of experience in GMP manufacturing operations, Bio-Pharma or Gene therapies preferred.Previous experience in QA Compliance including self‐inspections, health authority inspections and supplier auditing, preferably with a minimum of 2 year’s of experience as a lead inspector.Experience reviewing systems and analyze data (paper or electronic) to identify specific compliance and data consistency issues.Previous Quality Assurance experience required, including Data Integrity (ALCOA+) compliance.            Ability to apply a phase appropriate, risk‐based approach to QA operational decisions.Experience supporting cGMP manufacturing operations through administration and enforcement of the Quality Management System.Proficient in cGMP/ICH/FDA/EU regulations and guidelines and experience in US and international regulatory agency inspections a plus.Proficient in using Microsoft applications (MS Word, MS Excel, MS PowerPoint).Strong follow‐up and organizational skills and ability to manage cross functional projects.Experience with viral gene therapies and/or orphan disease indications a plus.Direct experience reviewing and/or authoring standard operating procedures.Ability to work well independently and within a team.Excellent oral and written communication skills with technical writing experience required.The salary for this position is expected to range between $73,500 and $136,500 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$73,500.00 - $136,500.00 Skills DesiredContinued Learning, Gmp Procedures, Managing Ambiguity, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technical Knowledge, Technological Intelligence Read Less

Job Description SummaryThe Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring of conformance to established quality processes and standards for manufacturing and production.Location: Durham, NC #LI-Onsite Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to ddPCR, ELISAs, NGS and Western Blot.Assists in the evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards.Reviews data obtained for compliance to specifications and reports abnormalities. Performs trend analysis of methods/environmental data/assay controls & standards and draws conclusions.Capable of delivering to assigned work schedule with attention to detail and accuracy.Support department risk assessments and participates in audit walk-throughs.Participates in the preparation of investigations, summaries and reports.Reviews data obtained for compliance to specifications and reportsInvestigates and resolves non-conforming test results by completing thorough Deviation, OOS/OOT/OOE and Investigation.Authors new/revise Standard Operating Procedures, Protocols / Summary Reports /Analytical Master Plans for QC.Oversees special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines.Supports training of departmental personnel in appropriate technique and related topics.Essential Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field requiredFor Specialist:  5 years’ experience in GMP environment or 4 years within Novartis Gene TherapiesFor Senior Specialist:  8 years’ experience in GMP environment or 7 years within Novartis Gene Therapies.Excellent interpersonal, verbal and written communication skills with strong technical writing experience required. Previous investigation experience a plus.Proven ability to work effectively in a team environment. Collaborates cross functionally with other departments to achieve site goals.Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action including critically thinking, troubleshooting and problem-solving skills.Normally receives general instructions on routine work, detailed instructions on new projects or assignments.Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties.The salary for this position is expected to range between $29.13/hr and $54.13/hr.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.Company will not provide visa sponsorship for this position.  Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.   EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$60,600.00 - $112,600.00 Skills DesiredContinued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management Read Less

Job Description SummaryThe Senior Analyst, Quality Control, Cell-based methods will support activities within the Quality Control department, with a focus on cell-based methods such as Adventitious Agents, rcAAV, potency, etc. This role will utilize laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), QC Methods & current Compendia. This role is based 100% on-site.Location: Durhan, NC #LI-OnsiteShift: 1st. Some night and weekend work may be required Job DescriptionKey Responsibilities:Executes routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to cell-based methods (potency, AA), PCR (ddPCR, qPCR), Immunoassays (ELISA), chromatography (HPLC-UV, HPLC-ELSD, HPLC-MS), AUC, compendial assays (Bioburden, pH) and electrophoresis (CE, Western Blot).  Ensures assigned to specific disciplines, but will support all necessary laboratory and assay functions, including housekeeping, safety, logbook/equipment use and maintenance, and updates to existing and authors new operating procedures. Capable of delivering to assigned work schedule with attention to detail and accuracy. Notifies management, initiates (such as Laboratory Investigations) and authors minor events/discrepancies in the quality systems, with little to no guidance from advisor or management. Understands the basic process improvement methodologies, learning and applying concepts of lean lab and six sigma that are applicable to the QC lab environment. May facilitate training to other team members in the organization. Ensures calibrates and maintains lab and analytical equipment are performed within established period. Conducts review of logbooks and may perform reviews as assigned by management May assist in drafting technical documents such as Protocols / Report to support method verification/validations. Other related job duties as assigned Essential Requirements:Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field with 2 years’ experience in GMP environment. Developing professional expertise, applies company policies and procedures to resolve a variety of issues.  Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.   Exercises judgment within defined procedures and practices to determine appropriate action including the critically thinking, troubleshooting and problem-solving skills.Normally receives general instructions on routine work, detailed instructions on new projects or assignments. Excellent interpersonal, verbal and written communication skills with strong technical writing experience required and ability to work in a team environment. Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties. Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $32.12/hour and $59.62/hour; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.  EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.  Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range$66,800.00 - $124,000.00 Skills DesiredAgility, Audit Management, Business Partnering, Continued Learning, Health Authorities, Influencing Skills, Knowledge Of Capa, Quality Management, Risk Management, Root Cause Analysis (RCA), Self-Awareness, Sop (Standard Operating Procedure), Technological Expertise Read Less

Compensation Details:Drivers earn on average $80000 a year!For a Limited Time we are offering at $10000 Sign On Bonus! Why should you join our team? We live our values - W.E.L.I.G.H.T (Winning, Excellence, Love, Integrity, Gratitude, Humility, and Teamwork). Gratitude. Humility. Love. You don’t often see values like these in most corporate statements, but Ace is different. These things are important to us. They represent our commitment to the company, our employees, to Ace retailers and to the Ace brand.In addition to providing our employees a great culture, Ace also offers competitive benefits* that address life’s necessities and perks, many of which expand and improve year after year, including:Weekly Pay (Additional pay for store deliveries, sleeper berths, backhauls, road closures, training)Driver incentive program to boost incomePaid Time Off Programs (incl. vacation, paid sick time, holiday pay). Newly hired full-time employees will receive a one-time pro-rated allocation of up to 24 hours of vacation in their first calendar year depending on the month of hire. Paid sick time in accordance with applicable state law. You will receive up to 9 holidays per year, depending on the month of hire.Comprehensive health coverage (medical, dental, vision and disability – up to 26 weeks short-term disability and long-term disability) & life insurance benefits for you and your dependents.Generous 401(k) retirement savings plan with a fully vested matching contribution the first year in addition to quarterly contributions and annual discretionary contribution (once eligibility requirements have been met). Over the past 5 years, company contributions (matching, quarterly & discretionary) for fully eligible employees have averaged 10.4% of total eligible compensationDriver Recognition ProgramCompany-paid HazMat Certification and DOT physicalsEmployer sponsored uniform programLong-term Career Opportunities: Many of our leaders started with Ace looking for a job, just like you, but found long-term career opportunities at our 15 Distribution Centers across the country and our Corporate Headquarters. Our company is growing, and we would love to have you grow with us!Merchandise Discounts on Top Brands like Weber, Traeger, Yeti, Craftsman, DeWalt and thousands more!Employee Assistance Program (EAP) – access to free visits to therapists and lawyers, guidance on financial matters, elder and childcare, and assistance with tickets to entertainment events.Tuition Reimbursement ProgramAdoption cost reimbursementIdentity theft protection* Benefits are provided in compliance with applicable plans and policies.Job Description:At Ace, “Helpful” is more than just a slogan—it’s at the core of everything we do. It guides the service we provide to our retailers and their communities, who are impacted daily by the quality of our operations and retail experience. We also take Helpful beyond our stores through our Ace Foundation, and its partnerships with Children’s Miracle Network Hospitals (CMN) and Habitat for Humanity, as well as through our employee-sponsored Ace Helpful Fund that provides emergency financial support to our own Ace team members in times of crisis. The spirit of Helpful can also be found within our values-driven company culture, in which team members live our W.E.L.I.G.H.T. Values every day to create a positive work environment for all. Within the Ace family, there’s always room for more Helpful, so join us today to be a part of what makes Ace the Helpful Place!Our Moxee, WA distribution center is looking for Professional Truck Drivers to make an impact and support our retailers with direct-to-store deliveries. Backed by a team of traffic and safety experts, Ace Drivers receive continuous support to ensure safety and efficiency when delivering product to Retailers and are one of the revered “Faces of Ace,” working independently to provide superior customer service and the Ace Helpful experience on and off the road.Safety is Our Number 1 Priority! With Safety as our number one priority, Ace is committed to maintaining a safe, healthy, and injury-free environment for all team members by supporting the latest and greatest safety programs and initiatives and practicing continuous improvement as new advancements become available. In addition, Ace Drivers are equipped with the industry-leading tools and equipment before hitting the road.Our RSC is located in Moxee, right outside of Yakima in Central WA and we service over 300 retailers all over WA, OR, ID, AK and part of MT. Our drivers do experience a variety of mountain terrain and intercity driving.This is a regional position which means you will usually run Sunday through Friday and are home 1-2 nights per week. Drivers do run unassigned for the first year or two, then they may be eligible for a route bid that allows for more of a structured schedule. Drivers are paid based on a combination of an hourly rate, by the mile and/or a handful of different pay components. Eligibility and RequirementsValid CDL with hazardous material endorsement (or 90 days to obtain)Minimum of 1-year Class A tractor/trailer on-road driving experience (or comparable experience)No suspensions/revocations or convictions of reckless driving in the past 3 years, or DUI/DWI in the past 5 yearsTo learn more and apply, please visit careers.acehardware.com or text "ACE" to 30914.Want to be notified when new jobs are posted? Follow the link below to create an account and set up custom job alerts:Create Job AlertWe want to hear from you!When most people think of career opportunities with Ace Hardware, they often think of the helpful cashiers and sales associates at their local store. However, have you also considered the people behind the scenes who select, promote, ship and process the invoices for more than 75,000 products? Maybe you haven't, but we'd like you to. Because together we help our customers take care of their homes. Come find out why a career with the Ace Hardware Corporation is one of America's best kept secrets.Equal Opportunity EmployerAce Hardware Corporation is committed to a policy of promoting equal employment opportunities. The company recognizes the importance of diversity and leveraging the skills and talents of all people to the mutual advantage of each individual and the organization. The company is committed to the prevention of employment discrimination related to race, religion, color, sex (including sexual harassment), gender identity, national origin, age, marital status, disability and military or veteran status, sexual orientation or any other action covered by federal or applicable state/local laws.DisclaimerThe pay range for this position starts as listed in the job posting, but could be higher based on education and experience. Please note, compensation decisions are dependent on the facts and circumstances of each opening. We take into consideration the minimum requirements outlined in the job description, such as an individual’s education, training and experience, the position’s work location, required travel (if any), and external market conditions when determining the final salary for potential new hires. Be aware that salary estimates published via alternate online job boards may not be a true representation of the actual pay range offered for this position. Please refer to the Ace position description for the accurate starting pay range information and feel free to discuss this with a Talent Acquisition professional if you are chosen to move forward with an interview. This written “Position Description” is not intended to cover all aspects of the position listed. It is meant to cover the basic/general essential job functions of a particular position. Ace Hardware Corporation reserves the right to change job duties, including essential job functions, according to business necessity.It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Read Less