As a member of the R&D Executive Leadership Team, this role holds a key leadership position within the R&D organizations of the CSL Enterprise. In this leadership role you will develop, implement, and maintain a forward-thinking Research Immunology/Transplant strategy and Vaccines strategy, in alignment with the overarching Therapeutic Leadership Teams for T&I and Vaccines.Main Responsibilities:Develop strategies to mitigate disruptive innovation for the plasma-derived Ig product portfolio Proactively contribute to all 5 TA strategies where immunology is a key driver Drive generation of scientific insights using internal and external expertise to progress projects and life cycle management goals in support of R&D and commercial products across the company Oversee CSL's interactions with multi-national government authorities key for developing and maintaining a vaccines product portfolio Strategic Leadership:Accountable for the Immunology & Transplant project portfolio and its turnover and maturation in alignment with the overall CSL therapeutic strategy Oversee new Research projects from target/pathway identification through to lead discovery and IND enabling studies Provide expert scientific leadership and advice to Immunology/Transplant TALT and cross TA opportunities based on related pathomechanisms Drive CSL's drug discovery to ensure development of a commercial portfolio that contributes to the company's vision of being a leading plasma biotech company Team Management:Lead a team of scientific SMEs: Research Product Leads & Disease Area experts to develop strategy and manage internal and external projects Leadership in a matrix working environment with relevant heads of drug development functions to ensure project delivery Research and Development:Drive scientific innovation by identifying novel targets, pathways, and therapeutic approaches in Immunology & Transplantation Ensure robust experimental design, data integrity, and scientific rigor across all research programs Foster a culture of scientific excellence and continuous learning within the team Translate scientific discoveries into viable therapeutic candidates aligned with unmet medical needs External Engagement:Leverage existing external network to build and maintain strong relationships with academic institutions, biotech partners, CROs, and key opinion leaders Represent the organization at scientific conferences, advisory boards, and in external collaborations Identify and evaluate external innovation opportunities, including licensing, partnerships, and acquisitions Serve as a scientific ambassador for the company's Immunology/Transplant research strategy Regulatory Compliance and Quality Assurance:Ensure all research activities comply with internal policies, ethical standards, and regulatory requirements Partner with Quality Assurance and Regulatory teams to support IND submissions and regulatory interactions Maintain accurate and auditable documentation of research activities and decisions Promote a culture of compliance, safety, and continuous improvement Innovation and Technology:Champion the adoption of cutting-edge technologies, platforms, and methodologies to enhance research capabilities Evaluate and implement digital tools, AI/ML, and high-throughput systems to accelerate discovery Encourage a forward-looking mindset that embraces scientific and technological advancements Lead initiatives to explore emerging trends and disruptive innovations in Immunology & Transplantation Required Qualifications:Advanced degree (Ph.D. or equivalent) in a relevant scientific discipline (e.g., pharmacology, biochemistry, molecular biology) Significant international experience (>15 years) and a proven track record in senior R&D leadership positions in the Pharma/Biotech industry with at least 10 years in a leadership or managerial role Demonstration of creating and executing on strategic initiatives Direct experience of end-to-end R&D development from project initiation through to launch Strong external network with academic institutions, biotech partners, CROs, and key opinion leaders (KOLs) Travel Requirements: This role will require 25% to 30% travel across various locations. Our Benefits We encourage you to make your well-being a priority. It's important and so are you. Learn more about how we care at CSL. About CSL CSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL . We want CSL to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL. Do work that matters at CSL!
The OpportunityThis position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations.Reporting compliance status data to operational quality managementCollaborate with center management in the development and implementation of continuous improvement plansCollaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concernsResponsible for coordinating and managing training activities, policies and processes at the center level.You will report to the Assistant Manager QualityThe RolePerform final QA review and release for all shipment and associated documents, to ensure shipment meets customer specifications.Ensure center records QA review to ensure thoroughness, accuracy and timeliness of required information. Initiate investigation and ensure documentation of regulatory deficiencies. Determine the need for corrective action, ensure appropriate documentation and determine effectiveness of the action.Perform center records QA review to ensure thoroughness, accuracy and timeliness of required information. Initiate investigation and ensure documentation of regulatory deficiencies. Determine the need for corrective action, ensure appropriate documentation and determine effectiveness of the action.Maintain and review Plasma center personnel training documents to ensure documents comply with CSL procedures, SOP's, CLIA/COLA and other applicable requirements.Maintain the Learning Management System to ensure data integrity, report generation and data analysis to comply with company and regulatory standards.Initiates schedule, coordinate and monitor the delivery of all training, such as new hire, annual and any retraining to meet center or other training and regulatory requirements. Ensure the most current version of training materials at the center is being usedCollaborates with center management when viewing the Quality Management System to identify, coordinate and deliver retraining for the purpose of correcting or improving operational or quality issues.Conduct periodic process assessments to ensure compliance of CSL written procedures. Initiate investigation to ensure documentation of deficiencies and development of corrective action plans, as necessary in partnership with management.Identifying and communicate non-conformities to CSL's SOP's. In the absence of the AQM, may conduct monthly quality team meeting to inform, promote, assess and identify opportunities for continuous process improvement in quality, safety, and training for implementation.Promote Safety, Health and Environment Policies & Procedure. Ensure safety training and safety practices are implemented and followed within the center.Conducts and may lead internal audits to monitor facility compliance with CSL procedures and policies, cGMP, OHSA, FDA, and other regulations, as applicable, and develop center responses for deficiencies. In the absence of the AQM, host external audits conducted by the regulatory agencies and customers.Responsible to initiate, investigate and close Trackwise reports in a timely manner. Confirm through follow-up, to ensure appropriate corrective action was initiated, implemented, and effective.Maintain clean efficient work environment. Comply with all Health Safety and Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Conduct routine internal procedure and documentation audits, as applicable.Follow all Standard Operating Procedures (SOPs), company policies and procedures.Comply with all local, state and federal regulations and laws to include, but not limited to: ADA, Civil Rights, EEOC, FDA, GHA, HIPAA, and OSHA.Maintain confidentiality of all personnel, donor and center information. Understand policies and procedures associated with hyperimmune programs at the center, if applicable.Assist Plasma center staff in completing other special projects or assignments, as requested.Perform other job-related duties, as assigned.dd 4-6 key responsibilities of the jobYour skills and experienceEducationHigh school diploma or equivalent required. Associate or Bachelor's degree in business administration or biological sciences preferred.ExperienceMinimum 1-year leadership experience or equivalent of one-year experience in a regulated environment.Strong customer service skillsStrong critical reasoning, decision-making and problem solving skills to analyze situationsOrganizational skills and attention to details to handle multiple tasks, short deadlines, frequent interruptions, and shifting priorities in support of changing company objectivesUnderstand Quality Systems and/or regulated training requirementsWorking Conditions(physical & mental requirements)Occasionally required to work with the public when they are dissatisfied80% of the time standing and walking and 20% of the time sittingReach, bend, kneel and have high level of manual dexteritySee and speak with customers and observe equipment operationOccasionally be required to lift and carry 25 lbs.Exposure to hot and cold temperatures, sudden temperature changes, working with freezers and various odorsOur BenefitsWe encourage you to make your well-being a priority. It's important and so are you. Learn more about how we care at CSL.About CSLCSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL .We want CSL to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL!
Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges? CSL Seqirus has an exciting opportunity for a Maintenance Apprentice in Holly Springs, NC. With a state of the art manufacturing facility and a deep expertise in influenza science, we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to collaborate. Together, we're working on the front line to protect communities from seasonal influenza and global pandemic threats. When you join CSL Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day.You Will:Be Enrolled in a Wake Tech Community College BioMechatronics Certificate Program in a cohort of North Carolina Life Sciences Apprentices from local pharmaceutical companies. The program includes the Electro-Mechanical and Mechatronics Technology program, Aseptic Processing I, Current Good Manufacturing Practices (CGMP), Writing Effective SOPs (WSOPs), and Cleanroom Gowning. Additional specialty courses OSHA 10, AHA CPR/First Aid/AED are included this program.Classes will be held at Wake Tech's Beltline Education Center (3200 Bush Street, Raleigh) and the Capstone Center (850 Oval Drive, Raleigh, NC - on NC State's Centennial Campus Monday - Friday from 7/28/2025 to 8/8/2025 and on Mondays and Tuesdays from 8/11/2025 to 3/26/2026 and will be funded by CSL Seqirus.Work onsite Wednesdays, Thursdays, and Fridays from 8AM to 5PM at our Holly Springs, NC facility from 8/11 /2025 to 2/26/2026 and Monday through Friday from 3/26/2026 until program completion July 2026 and rotate between Facilities, Utilities, HVAC/Refrigeration, Calibrations, and Process Maintenance teams to gather knowledge on all aspects of Pharmaceutical Maintenance.Repair, install, inspect, adjust, troubleshoot, and maintain pharmaceutical production and processing machinery and utility distribution systems.Learn how to track and monitor equipment performance to prevent equipment failures.Learn how to adjust, setup, calibrate, and complete alignments on conventional production equipment.Monitor and respond to equipment and Building Automation System alarms.Follow standard operating procedures for preventative and corrective maintenance.Comply with all GxP guidelines and compliance requirements for maintenance practices and documentation.Execute Maintenance Work orders in a CMMS system.Clean and move materials into a GMP controlled classified areas.Upon successful completion of the 1 year program and course requirements, receive a Journeyworker Apprenticeship Certificate from the United States Department of Labor and the North Carolina Community CollegesMinimum Qualifications:High school diploma/GED requiredBe willing to be enrolled and successfully complete the Wake Tech Community College BioMechatronics Certificate Program during the 1 year program. This training course is designed to meet industry demands for highly skilled technicians in the mechatronics field through instruction that leads to competency-based certifications. Upon successful completion of the course, students will be equipped to work in a manufacturing environment and earn SACA (Smart Automation Certification Alliance) micro-credentials in the following areas:Electrical SystemsMotor Control SystemsPneumatic SystemsMechanical Power SystemsExperience applying mathematical concepts in a professional or industry setting is preferredBasic mechanical aptitude and knowledge of hand toolsSuggested Pre-requisites and Certificate requirements:Have completed NC BioWork Certificate Program (Pre-Apprenticeship).Our BenefitsCSL Seqirus employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL Seqirus offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.Please take the time to review our benefits site to see what's available to you as a CSL Seqirus employee.About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL Seqirus .We want CSL Seqirus to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL Seqirus!Watch our 'On the Front Line' video to learn more about CSL Seqirus
As the Senior Director of Sales Operations & COE you will play a key role with responsibility for leading all aspects of sales force operations across the entirety of CSL Behring's US portfolio of products and sales teams. This role will leads efforts including sales force sizing and organizational design, sales customer targeting, incentive program strategy and deployment, sales force reporting, customer and sales force analysis and insight, recommendations for improvements in sales force effectiveness, and deployment of tools in the US market (including CRM) to enhance sale force and operational productivity.
The role requires synthesis of exceptional leadership, collaboration and analytical skills with the incumbent leading multiple cross functional projects and operations in parallel within the sales operations function and related sub-functions (Targeting/Alignment/Reporting, Incentive Compensation). Operates as a key member of the US Insights & Analytics leadership team and strategic business partner to the US sales and marketing leadership teams.
Main Responsibilities and Accountabilities:
Leadership: Leads the Sales Operations team across all work streams (targeting/alignment, reporting, sales incentives, sales analytics, sales data, CRM) providing priority setting, planning, and timely decision making of activities to ensure value delivery to all internal and external customers. Encourage a culture of innovation and continuous improvement. Represent Sales Operations on the Strategic Analytics & Pricing leadership team.Sales Incentives: Lead a cross functional team (including analytics, sales and marketing leadership) to develop quarterly/semesterly sales incentive compensation plans across US portfolio that promote alignment between CSL strategic objectives and field force activity. Oversee annual performance awards, program modeling, and implementation of approved sales incentive programs. Responsible for leading governance and related processes associated with sales incentive plans.Sales Force Alignment: Own sales force sizing, territory design, and alignment processes. Oversee the analytical effort for field force alignments, both major and minor. Ensure sales force deployment is consistent with company, brand and sales strategies and the CSL sales organization is deployed to optimally interact and promote CSL products to our customers. Ensure the alignments are sound pre and post implementation.Sales Force Targeting: Oversee the process and analysis to translate brand strategic and tactical intent into action-oriented plans for CSL customer interactions. Provide analytics to identify customers with greatest opportunity and promotional sensitivity and work with cross functional stakeholders to prioritize and optimize sales resource deployment against CSLs target customers. Operationalize customer targets across the sales force including executional oversite of planned activities.CRM: Own CRM operations for US sales and customer facing teams. Represents the US commercial organization needs on the global CRM (Veeva) operating committee within the global organization. Supports the ongoing development of initiatives across various functional areas including Sales, Medical and Marketing.Global COE: Serve as a strategic advisor to U.S. and global commercial leadership, shaping the direction of field operations and sales excellence. Establish and lead the Global Sales Operations COE, standardizing tools, metrics, and processes across geographies. Drive alignment between regional and global stakeholders to ensure consistency in operations while enabling local customization where needed. Collaborate with the BE&Ops and IT team to identify, evaluate, and implement new technology solutions that support the CoE's objectives, drive efficiencies, and enhance data-driven decision-making.Management: Responsibility for oversight and effective management of all team members (i.e. direct reports) to include but not limited to the following
Annual objective setting
Mid-year and end of year review
Coaching and counseling as appropriate
Employee development
Recruitment, selection and development of talent
Managing, directing & measuring work on an ongoing basis. Provides timely constructive feedback to ensure quality of work meets or exceeds company standards
Assuring work is completed in a customer focused manner
Education
BA or BS required in Finance, Accounting, or Business or related field required.
MBA Highly Preferred
Experience
-15+ years professional experience, 8+ years' experience within the pharmaceutical industry.
-Experience in specialty/rare disease data strongly preferred including acquisition and integration of specialty pharmacy data and use of secondary claims data (e.g. IQVIA claims data)
-Experience across all areas of sales operations including sales incentive compensation design and operations, customer targeting, sales force alignment, analytics & reporting, leveraging associated information technology support systems
-Advanced analytical skills in Microsoft Office (Excel/Access/PowerPoint); Experience with -BI tools such as Power BI, Tableau preferred. Veeva knowledge preferred.
-8+ years of experience with CRM
-Multiple years' experience leading and managing teams in an international and matrixed environment-Excellent negotiation, communication, and relationship-building abilities-Strong Change and Leadership skills
Our BenefitsCSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.Please take the time to review our benefits site to see what's available to you as a CSL employee.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring .We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL Behring!
Responsibilities:
• Under direct supervision, assists with the setup and operation of production equipment
• Operates manufacturing equipment following standard procedures and current Good Manufacturing Practice (cGMP)
• Determines and corrects minor machine malfunctions
• Enters data for process control, departmental databases and spreadsheets
• Performs routine maintenance and cleaning
Qualifications:
• High School Diploma or equivalent vocational or technical training
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.Our BenefitsCSL offers the following benefits for this full-time position: Options for health care benefits, including choices of plans for medical, dental, and vision, prescription drug coverage; Company-provided basic life insurance and Short- and Long-Term Disability; the option to participate in CSL's 401(k) Savings Program; Paid Time Off (PTO) for use in connection with vacations, illness, and other personal business; and paid observed holidays as designated by the Company. For more information on CSL Plasma benefits visit .About CSLPlasmaCSL Plasma is one of the world's largest collectors of human plasma. Our work helps to ensure that people with rare and serious diseases are able to live normal, healthy lives. We are committed to our work because lives depend on us. Learn more about CSL Plasma .We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Plasma!
You will initially report into the Senior Director of New Product Planning & Evidence Strategy and will transition to Executive Director, Specialty Marketing three months prior to launch. You will have direct reports in this role.Responsibilities:As the Director of Marketing you will be responsible for launching RIASTAP in the US, with full P&L accountability for the brand. This pivotal role is essential in shaping and developing the market to unlock a multi-billion-dollar opportunity in Patient Blood Management (PBM), while achieving net sales and market share goals for RIASTAP. Collaborating with Sales, Healthcare Systems, Pricing and Contracting, Insights and Analytics, Payer Marketing, and Medical Affairs, the Director ensures that strategies are robust, impactful, and aligned with the overall brand and PBM vision. Additionally, the Director defines and drives synergies with other major brands in the portfolio to strengthen market leadership and maximize portfolio value. Engaging cross-functional leaders, the Director translates customer needs into effective initiatives and ensures these initiatives are executed with urgency to exceed brand objectives. This role demands independent work with a strong focus on excellence, customer centricity, and outcomes, while influencing cross-functional partners and senior management.Successfully launch RIASTAP in the US to realize multi-billion-dollar opportunity in the Patient Blood Management (PBM) and meet or exceed revenue and market share goals for RIASTAP.Develops and presents strategic and tactical plans to U.S. Commercial Leadership as part of the Integrated Business Planning (IBP) process. In collaboration with Sales, Healthcare Systems, Pricing and Contracting, Insights and Analytics, Payer Marketing, and Medical Affairs, ensures that brand strategies are robust, impactful, and aligned with the overall brand and PBM vision.Translates customer needs into effective cross-functional initiatives and ensures these initiatives are executed with urgency.Accountable for the successful implementation and measurement of these plans to meet brand objectives.Identifies customer needs for evidence and lifecycle management and act as a brand champion to ensure those needs are prioritized.Accountable for production plan forecasting, including gaining stakeholder input on projections. Responsible for the effective management and operation marketing activities within the approved budget.Responsibility for defining and driving synergies with other brand/s in the portfolio to strengthen market leadership and maximize portfolio value.Develops and manages effective agency relationships in support of key initiatives.Manages agency partners to deliver on brand and customer needs in support of brand objectives. Optimizes spends on external partner's support.Build and leverage effective and productive working relationships with key external customers, including thought leaders and professional societies.Hires, manages and develops top talent.Education:BS/BA, MBA preferredExperience:10+ years relevant health care marketing and commercial planning experience including experience with launch of product or line extensions.3+ years of people management preferredInstitutional/hospital experience preferredThe position requires excellent organizational skills, collaboration, teamwork, and the ability to manage multiple projects with tight deadlines in a fast paced environmentOur BenefitsCSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.Please take the time to review our benefits site to see what's available to you as a CSL employee.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring .We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL Behring!
Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges? Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With the state-of-the-art manufacturing facility and an expertise in influenza science we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to collaborate.Together, we're working to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day.Reporting to the Manager, Manufacturing Quality Systems, you will work onsite at our Holly Springs, NC facility. Our benefits include an Onsite Café, 1/2 mile Walking Trail, Basketball and Tennis Courts; access to Medical, Dental, Vision, Life Insurance, 401K with a 6% match and an annual bonus; and accrued PTO, wellness days and floating holidays.Responsibilities:Lead a cross functional deviation investigation team.Use root cause analysis tools and experience to determine root cause of deviations.Utilize technical writing to author deviation reports in the Quality Management System.Define CAPA plans to prevent reoccurrence of deviations.Author and/or supports product impact assessments.Manage corrective actions to prevent deviations.Own change controls and projects to support manufacturing operations.Qualifications:Bachelor's degree in Science or Engineering or equivalent industry experience required.Minimum of 1 years of experience conducting deviation investigations, root cause analysis, CAPA management , and Change Controls or equivalent experience in the pharmaceutical industry.Direct experience within a cGMP environmentDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.Our BenefitsCSL Seqirus employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL Seqirus offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.Please take the time to review our benefits site to see what's available to you as a CSL Seqirus employee.About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL Seqirus .We want CSL Seqirus to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL Seqirus!Watch our 'On the Front Line' video to learn more about CSL Seqirus
Responsibilities1. Following current good documentation and manufacturing practices to build high quality product per SOP's2. Inspecting product for rejects including leakers, illegible label copy, missing components, etc. per SOP's.3. Loading of sterilizer carts per validated cycle configurations per SOP's.
4. Meet production schedule daily.
5. Operation of equipment such as Printing Machines, Filling Machines, Overpouch Machine and Pallet Jack.
6. Packing product and palletizing per appropriate SOP's
7. Sanitization of work area as per SOP's.
8. May perform material handling duties as required.
9. Perform other job-related duties as assigned.
Job SpecificationsEducation:High School Diploma or equivalent is required
Experience:Minimum of one (1) year experience in operating equipment, preferably in production environment is requiredAdditional Comments:Proactively approaches responsibilitiesFriendly and service-orientedDemonstrates a high commitment to qualitySeeks to acquire knowledge in area of specialtyStrong verbal communication and listening skillsExcellent collaboration and team building skillsWorking Conditions (physical & mental requirements):Fast-paced environment with frequent interruptionsAbility to lift and carry up to 50 lbs.Standing frequently up to 75% of the timeSitting, walking, bending and twisting up to 25% of the timeUse hands to reach, finger, handle or feel objects, tools or controlsShares information with internal contacts with common desire to reach a solutionAbility to understand, remember and apply oral and/or written instructionsAbility to make decisions which have moderate impact on immediate work unitAbility to complete routine forms or conduct routine oral communicationsAbility to add, subtract, multiply, divide and to record, balance and check results for accuracyFrequently required to wear personal protective equipmentOccasionally exposed to hazardous chemicalsNote: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual
orientation, gender identity, disability, veteran status, national origin or other legally protected classifications.Our BenefitsCSL offers the following benefits for this full-time position: Options for health care benefits, including choices of plans for medical, dental, and vision, prescription drug coverage; Company-provided basic life insurance and Short- and Long-Term Disability; the option to participate in CSL's 401(k) Savings Program; Paid Time Off (PTO) for use in connection with vacations, illness, and other personal business; and paid observed holidays as designated by the Company. For more information on CSL Plasma benefits visit .About CSLPlasmaCSL Plasma is one of the world's largest collectors of human plasma. Our work helps to ensure that people with rare and serious diseases are able to live normal, healthy lives. We are committed to our work because lives depend on us. Learn more about CSL Plasma .We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Plasma!
As the Director of HIZENTRA, you will be responsible for the development and execution of marketing strategies to achieve business objectives and goals. You will work with internal and external partners to gain insights on the HCP and patient communities to create brand strategies, optimize the customer experience and pull tactical plans through to execution. You will identify and lead development of digital and non-digital assets such as web, social, mobile, print materials as well as innovative tactics to create a complete customer experience and multichannel marketing approach. The role will also be responsible for leading cross functional team meetings, using insights to develop strategic business plans and measurement to optimize marketing campaigns. You will be part of a high-performing team focused on customer engagement and experience. You must be able to work independently with minimum guidance from the Senior Director while being able to influence cross functional partners and senior management.Key Responsibilities:Strategic Planning: Develop and implement comprehensive marketing strategies for HCPs and patients that align with HIZENTRA's business objectives and achieve growth targets. Develop KPIs, track performance and optimize marketing programs for maximum impact.Asset Development: Lead the development and management of HCP and patient communication strategies, ensuring consistent messaging across all channels. Develop messaging that improves the patient / physician dialogue and drives patients to ask their physicians for HIZENTRA.Market Analysis and Research: Conduct thorough market analysis to identify opportunities, trends, and challenges within the rare disease market. Develop strategies to overcome barriers. Stay up to date on evolving market dynamics and competitors.Product Launches: Plan and execute successful indication launches and/or label updates, including the development of go-to-market strategies, promotional materials, and educational resources.Stakeholder Engagement: Build and maintain relationships with key stakeholders, including patients, healthcare professionals, advocacy groups, and industry partners.Digital Marketing: Oversee the development and execution of digital marketing campaigns, including social media, content marketing, and online advertising.Cross-Functional Collaboration: Work closely with cross-functional teams, including Sales, Medical Affairs, Market Access, Patient Services/Engagement, Public Affairs, Legal and Regulatory, to ensure alignment and successful execution of marketing strategies and brand priorities.Agency Management: Lead agency partners in the develop and implementation of strategic and tactical plans to drive brand growth.Budget Management: Oversee project budgets, ensuring efficient allocation of resources to maximize ROI.Qualifications:Experience: Minimum of 12+ years of marketing experience in the biotechnology or pharmaceutical industry, rare disease experience preferred. Sales and/or Market Access experience preferred.Education: Bachelor's degree in marketing, business, or a related field. MBA preferred.Expertise: Deep understanding of the immunology or rare disease market preferred, including regulatory requirements, patient advocacy, and market access challenges.Skills: Strong leadership, communication, and analytical skills, with the ability to think strategically and lead flawless execution. Innovation: A creative and innovative mindset, with a passion for making a difference in the lives of patients with rare diseases.Travel: Willingness to travel as needed (up to 20%)Our BenefitsCSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.Please take the time to review our benefits site to see what's available to you as a CSL employee.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring .We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Behring!
As a member of the R&D Executive Leadership Team, this role holds a key leadership position within the R&D organizations of the CSL Enterprise. In this leadership role you will develop, implement, and maintain a forward-thinking Research Immunology/Transplant strategy and Vaccines strategy, in alignment with the overarching Therapeutic Leadership Teams for T&I and Vaccines.Main Responsibilities:Develop strategies to mitigate disruptive innovation for the plasma-derived Ig product portfolioProactively contribute to all 5 TA strategies where immunology is a key driverDrive generation of scientific insights using internal and external expertise to progress projects and life cycle management goals in support of R&D and commercial products across the companyOversee CSL's interactions with multi-national government authorities key for developing and maintaining a vaccines product portfolioStrategic Leadership:Accountable for the Immunology & Transplant project portfolio and its turnover and maturation in alignment with the overall CSL therapeutic strategyOversee new Research projects from target/pathway identification through to lead discovery and IND enabling studiesProvide expert scientific leadership and advice to Immunology/Transplant TALT and cross TA opportunities based on related pathomechanismsDrive CSL's drug discovery to ensure development of a commercial portfolio that contributes to the company's vision of being a leading plasma biotech companyTeam Management:Lead a team of scientific SMEs: Research Product Leads & Disease Area experts to develop strategy and manage internal and external projectsLeadership in a matrix working environment with relevant heads of drug development functions to ensure project deliveryResearch and Development:Drive scientific innovation by identifying novel targets, pathways, and therapeutic approaches in Immunology & TransplantationEnsure robust experimental design, data integrity, and scientific rigor across all research programsFoster a culture of scientific excellence and continuous learning within the teamTranslate scientific discoveries into viable therapeutic candidates aligned with unmet medical needsExternal Engagement:Leverage existing external network to build and maintain strong relationships with academic institutions, biotech partners, CROs, and key opinion leadersRepresent the organization at scientific conferences, advisory boards, and in external collaborationsIdentify and evaluate external innovation opportunities, including licensing, partnerships, and acquisitionsServe as a scientific ambassador for the company's Immunology/Transplant research strategyRegulatory Compliance and Quality Assurance:Ensure all research activities comply with internal policies, ethical standards, and regulatory requirementsPartner with Quality Assurance and Regulatory teams to support IND submissions and regulatory interactionsMaintain accurate and auditable documentation of research activities and decisionsPromote a culture of compliance, safety, and continuous improvementInnovation and Technology:Champion the adoption of cutting-edge technologies, platforms, and methodologies to enhance research capabilitiesEvaluate and implement digital tools, AI/ML, and high-throughput systems to accelerate discoveryEncourage a forward-looking mindset that embraces scientific and technological advancementsLead initiatives to explore emerging trends and disruptive innovations in Immunology & TransplantationRequired Qualifications:Advanced degree (Ph.D. or equivalent) in a relevant scientific discipline (e.g., pharmacology, biochemistry, molecular biology)Significant international experience (>15 years) and a proven track record in senior R&D leadership positions in the Pharma/Biotech industry with at least 10 years in a leadership or managerial roleDemonstration of creating and executing on strategic initiativesDirect experience of end-to-end R&D development from project initiation through to launchStrong external network with academic institutions, biotech partners, CROs, and key opinion leaders (KOLs)Travel Requirements:This role will require 25% to 30% travel across various locations.Our BenefitsWe encourage you to make your well-being a priority. It's important and so are you. Learn more about how we care at CSL.About CSLCSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL .We want CSL to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.Do work that matters at CSL!
