Laboratory Equipment Calibration & Qualification Engineer
Company: Synergy Bioscience
Job Type: Full-Time
Synergy is seeking an experienced, hands-on Laboratory Equipment Calibration & Qualification Engineer to support our pharmaceutical and biotech laboratory operations. This is a technically focused role designed for professionals who thrive in active laboratory environments and are committed to maintaining the highest standards of instrument accuracy, regulatory compliance, and operational reliability. If you have a passion for precision and a proven track record in laboratory instrumentation, we want to hear from you.
Role Overview
The Laboratory Equipment Calibration & Qualification Engineer will serve as the technical backbone of our laboratory infrastructure, ensuring that all instruments and equipment perform to their validated specifications. This is not a managerial position; it is a direct, hands-on role that requires deep technical expertise and a proactive approach to equipment performance management.
Requirements
Education and Experience
Bachelor's degree in Engineering or a related technical discipline.Minimum of 5 years of direct, hands-on experience in laboratory equipment maintenance, qualification, and calibration.Proven experience within a pharmaceutical or biotech environment, with a strong working knowledge of cGMP standards and laboratory quality system requirements.Demonstrated proficiency with a wide range of laboratory instruments, calibration tools, and specialized calibration software.Skills
Technical Troubleshooting: Strong technical and troubleshooting skills across a diverse range of laboratory instruments, with the ability to diagnose and resolve both mechanical and software-related failures efficiently and effectively.Documentation Excellence: Exceptional documentation and record-keeping abilities, ensuring that all calibration, maintenance, and qualification activities are recorded with the accuracy and completeness required for regulatory audits and internal reviews.Communication and Vendor Management: Effective communication skills combined with proven vendor management experience, enabling seamless coordination with external service providers and clear alignment with internal cross-functional stakeholders.Independent and Collaborative Work Style: Demonstrated ability to manage a complex personal workload with minimal supervision while contributing meaningfully to cross-functional team projects involving quality assurance, facilities, and research and development.On-Site Readiness: Ability to work effectively in an on-site laboratory environment.Benefits
Benefits
Health Care Plan: Synergy offers a comprehensive Health Care Plan covering Medical, Dental, and Vision services, designed to support the overall well-being of our employees and their families.Paid Time Off: We provide a generous Paid Time Off policy that includes Vacation days, floating holidays, and all major Public Holidays, reflecting our commitment to a healthy and sustainable work-life balance for every member of our team.Training and Development: Synergy invests in its people through robust Training and Development programs, including ongoing learning opportunities to ensure our engineers remain at the cutting edge of laboratory qualification and calibration technology. Read LessQA/RA Specialist - Pharmaceutical GLP/GMP Experience
Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. This role involves reviewing procedures, ensuring documentation compliance, conducting internal audits, and assisting with regulatory submissions and inspections.
Key Responsibilities:
Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies.Conduct internal audits and inspections to assess compliance with quality systems and regulatory standards.Support preparation and management of regulatory submissions and responses to regulatory agencies.Collaborate with cross-functional teams to ensure compliance throughout product lifecycle.Assist in training laboratory and manufacturing staff on quality system requirements and regulatory standards.Investigate and support resolution of deviations, non-conformances, and CAPA activities.Education & Experience:
Bachelor’s degree in life sciences, pharmacy, chemistry, or related field.Minimum 5 years of experience in pharmaceutical GLP/GMP quality assurance and regulatory affairs.Strong knowledge of FDA, EMA regulations, and ICH guidelines.Experience with internal auditing and regulatory inspections.Requirements
Education:
Bachelor’s degree in life sciences, pharmacy, chemistry, or a related discipline.Experience:
At least 5 years of hands-on experience in pharmaceutical GLP/GMP QA and regulatory affairs.Familiarity with international regulatory frameworks including FDA, EMA, and ICH guidelines.Proven experience conducting internal audits and supporting regulatory inspections.Skills:
Strong attention to detail and organizational skills.Excellent communication and interpersonal abilities.Ability to work collaboratively with cross-functional teams and manage multiple priorities.Proficiency in quality management systems and documentation practices.Benefits
Health Care Plan (Medical, Dental & Vision)Paid Time Off (Vacation, Sick & Public Holidays)Training & Development Read LessChemist
Synergy is looking for a motivated Chemist to join our dynamic team. The ideal candidate will have a solid background in chemistry and laboratory experience to support research and development, quality control, or manufacturing processes across pharmaceutical or biotech projects. The Chemist will conduct experiments, analyze data, prepare reports, and maintain laboratory equipment while adhering to regulatory and safety standards.
Key Responsibilities:
Conduct chemical analyses and experiments following standard operating procedures (SOPs).Develop, optimize, and validate analytical methods.Maintain accurate and detailed records of experimental data.Operate and maintain laboratory instruments and equipment.Collaborate with cross-functional teams including R&D, QC, and manufacturing.Ensure compliance with GMP, safety, and environmental regulations.Assist in troubleshooting analytical or process issues.Education & Experience:
Bachelor’s degree in Chemistry or related scientific discipline.Minimum 10 years of laboratory experience in pharmaceutical, biotech, or chemical industry.Familiar with analytical techniques such as HPLC, GC, GC-MS, LC-MS, Dissolution Apparatus, TOC, or any other.Working knowledge of GMP, safety, and quality standards.Requirements
Education:
Bachelor’s degree in Chemistry or related field.Experience:
10+ years of experience in laboratory settings within pharmaceutical, biotech, or chemical industries.Experience operating analytical instruments.Skills:
Strong analytical and problem-solving skills.Good communication and teamwork abilities.Attention to detail and ability to maintain precise records.Benefits
Competitive Salary Health Care Plan (Medical, Dental & Vision)Paid Time Off (Vacation, Sick, floating & Public Holidays)Training & Development Read LessDigital Marketing Specialist
Synergy is looking for a creative and results-driven Digital Marketing Specialist to join our marketing team. The ideal candidate will be responsible for developing, implementing, and managing digital marketing campaigns that promote our CRO services in the pharmaceutical, biotech, and medical device sectors. This role involves leveraging digital channels, including SEO, SEM, email marketing, social media, Google Ads, LinkedIn Page, and content marketing, to increase brand awareness, generate leads, and support sales growth.
Key Responsibilities:
Develop and execute digital marketing strategies aligned with company objectives.Manage and optimize campaigns across SEO, PPC, social media, email marketing, and content marketing channels.Analyze website traffic and campaign performance using analytics tools, providing insights and recommendations.Collaborate with content creators to produce engaging and informative marketing materials.Coordinate with sales and business development teams to align marketing activities with lead generation goals.Stay up to date on digital marketing trends and emerging technologies to enhance the company’s online presence.Manage the company’s social media profiles and engage with relevant online communities.Education & Experience:
Bachelor’s degree in Marketing, Communications, or related field.5+ years of experience in digital marketing, preferably in the pharmaceutical, biotech, or scientific services sectors.Proficiency with digital marketing tools such as Google Analytics, Google Ads, SEO tools, and email marketing platforms.Strong analytical skills and a data-driven mindset.Excellent written and verbal communication skills.Requirements
Experience:
10+ years of experience in digital marketing, preferably within pharmaceutical, biotech, or CRO environments.Proven experience managing multi-channel digital campaigns.Familiarity with SEO, SEM, email marketing, Google Ads, and social media marketing strategies.Skills:
Proficiency in analytics and digital marketing tools (Google Analytics, Google Ads, SEO software).Strong communication, writing, and content creation abilities.Ability to analyze data and optimize marketing performance.Team-oriented with the ability to collaborate across departments. Read LessOrganic Synthetic Chemist
Synergy is seeking an experienced Organic Synthetic Chemist to join our research and development team. The ideal candidate will have strong expertise in designing and executing synthetic routes for complex organic molecules, supporting pharmaceutical and biotech projects. This role will involve collaboration with cross-functional teams to develop, optimize, and scale-up synthetic methods while ensuring high-quality and reproducible results in compliance with regulatory standards.
Key Responsibilities:
Design and perform multi-step organic syntheses to produce target molecules for drug development.Develop and optimize synthetic routes to improve yield, purity, and scalability of enantiomeric chemicals.Document experimental procedures, data, and results accurately in lab notebooks and reports.Collaborate with analytical scientists to support project goals and timeline. Ensure compliance with safety, GMP, and regulatory requirements in all laboratory activities.Troubleshoot synthetic scheme challenges, characterization data, and reaction conditions, and propose innovative solutions.Education & Experience:
Master’s degree in Chemistry or higher degree in chemistry with a focus on stereochemistry and enantiomeric synthesis.Minimum 10 years of experience in synthetic organic chemistry, preferably in pharmaceutical or biotech settings.Strong knowledge of stereochemistry, synthetic methodologies, reaction mechanisms, and analytical techniques.Experience with GMP environment and documentation is preferred.Requirements
Skills:
Strong problem-solving skills and innovative thinking in organic synthetic design.Excellent documentation and laboratory practices.Effective communication and teamwork capabilities.Benefits
Competitive Salary Health Care Plan (Medical, Dental & Vision)Paid Time Off (Vacation, Sick & Public Holidays)Training & Development Read LessManager, New Business Development
Location: United States (Remote – National Territory)
Travel: ~40–50%
Overview
Synergy Bioscience is a Contract Research, Development, Testing, and Consulting Organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies across the drug development lifecycle. We are seeking a Manager of New Business Development to lead commercial expansion across the United States. This individual will drive new business opportunities for CRO services with biotech, pharmaceutical, and medical device companies. The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting, and a proven ability to partner with clients to accelerate product development and testing and ensure regulatory readiness.
This is a high-impact role responsible for identifying strategic partnerships, managing the full sales cycle, and expanding national revenue growth.
Key Responsibilities
Business Development & Sales
Develop and execute a national business development strategy targeting biotech, pharmaceutical, and medical device companies.Identify and secure new clients requiring analytical testing, pharmaceutical development, microbiology testing, and regulatory consulting services.Manage the full sales cycle, including prospecting, qualification, proposal development, negotiation, and closing.Build relationships with R&D, CMC, Quality, and Regulatory leaders within target organizations.Represent the company at industry conferences, trade shows, and networking events.Strategic Account Development
Establish and grow relationships with emerging biotech, mid-size pharma, and device companies.Expand services within existing client accounts.Partner with internal scientific teams to translate client needs into technical solutions and proposals.Market Intelligence
Track industry trends within drug development, analytical testing, and regulatory compliance.Provide competitive intelligence and market insights to leadership.Identify opportunities for new service offerings or expansion areas.Cross-Functional Collaboration
Work closely with scientists, laboratory leadership, and project management teams to ensure client success.Support proposal development and pricing strategy.Assist in strategic partnerships and long-term client agreements.Requirements
Qualifications
Bachelor’s degree in Life Sciences, Chemistry, Biology, or related field.10+ years of business development experience within:CROCDMOAnalytical testing labsPharmaceutical development servicesDemonstrated success selling services such as:Analytical chemistryMicrobiology testingPharmaceutical developmentRegulatory consultingStrong network within biotech/pharma R&D or CMC organizations.Proven ability to generate new revenue and close complex service deals.Benefits
- Competitive salary
- Commissions for every new project.
- End-of-year bonuses.
- Healthcare, dental, and vision insurance.
- PTO and floating holidays.
Read LessPharmaceutical GMP QA Specialist
Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible for implementing and maintaining quality management systems, conducting inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration with the development and testing teams to maintain compliance with the regulatory requirements.
Key Responsibilities:
Ensure adherence to pharmaceutical GMP regulations and internal quality standards.Conduct routine and for-cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories.Review and approve GMP-related documentation, including test results, technical reports, investigation reports, and SOPs.Coordinate with cross-functional teams to address non-conformities and implement corrective and preventive actions (CAPAs).Support regulatory inspections and manage responses to audit findings.Monitor quality metrics and report on compliance status.Provide training and guidance on GMP requirements to laboratory personnel.Education & Experience:
Bachelor’s degree in Chemistry or Microbiology.Minimum 10 years of experience in pharmaceutical quality assurance with strong knowledge of GMP regulations.Experience working within the FDA, DEA, and ISO 17025.Proven ability to conduct audits and manage quality documentation.Strong communication, analytical, and interpersonal skills.Requirements
Education:
Bachelor’s degree in Chemistry or Microbiology.Experience:
10 + years of experience in pharmaceutical quality assurance or GMP compliance.Familiarity with the FDA, DEA, and the iSO 17025 regulations and requirements.Experience in conducting audits and managing quality systems.Skills:
Strong analytical and problem-solving abilities.Excellent communication and interpersonal skills.Ability to work collaboratively in cross-functional teams.Benefits
Health Care Plan (Medical, Dental & Vision)Paid Time Off (Vacation, Sick & Public Holidays)Training & Development Read LessQA Lead Auditor – With Previous FDA Audit Experience.
This position will be responsible for planning and conducting audit procedures, including identifying and defining audit issues, developing audit criteria, reviewing and analyzing evidence, documenting the status and operating procedures of the organization, and preparing audit reports. The Lead Auditor will be responsible for the assessment of the organization’s quality system and compliance status in accordance with all relevant regulations and guidelines, such as 21CFR Parts 211, Parts 600s, Parts 3 &4, as well as Part 820. The lead auditor will independently perform quality audits of drug product manufacturing practices to ensure products, controls, procedures, and processes meet quality standards. The Lead Auditor will also prepare audit reports and communicate findings to stakeholders.
Responsibilities:
· Able to perform high-profile audits for manufacturing facilities and clinical trial sites.
· Lead a team of auditors, conduct manufacturing sites audits, and identify and follow up on any resolved audit findings identified during a Quality Assurance Audit.
· Adheres to all safety, environmental, and quality requirements, not limited to: Quality Management Systems (QMS), U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
· Schedules audit activities with the internal sites and provide audit agenda.
· Writes audit reports of findings, recommendations, and management corrective action plans.
· Assure that issues from sponsor audits are promptly communicated to the appropriate team
· Tracks audit responses and auditees’ remediation CAPAs until completion and closeout.
· Independently performs evaluations of quality systems and practices to identify potential problems
· Stays up to date on current FDA and Health Canada manufacturing trends
Education & Experience & Knowledge & Skills:
· Previous work experience with FDA or Health Canada Agencies is a requirement.
· Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
· Thorough knowledge of current standard practice and regulations
· Ability to review technical documents
This unique opportunity provides:
· Exceptional hourly rates on 1099 or C2C.
· Reimbursement of all expenses while working on the project.
Requirements
Education & Experience & Knowledge & Skills:
· Previous work experience with FDA regulations and GMP requirements is required.
· Minimum of a BS degree in science with a minimum of 5+ years of experience in performing and discussing audits.
· Thorough knowledge of current standard practice and regulations
· Ability to review technical documents
Location:
· Hybrid work style with requirements to travel overseas to perform onsite audits
Benefits
This unique opportunity provides:
· Exceptional hourly rates on 1099 or C2C.
· Reimbursement of all expenses, while working on the project.
Read Less