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Quality Control Bioanalytical Jobs (NOW HIRING)

Senior QC Biochemist

Silver Spring, MD · On-site

$92.50K - $120K/yr

... bioanalytical and analytical method development/validation * Proficiency in cGMP documentation and regulated laboratory practices, including use of electronic quality and data management systems ...

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

We are seeking an experienced Quality Assurance Manager to support our Translational Science ... document control) * Experience supporting or leading FDA inspections for bioanalytical labs

Lab Technician I, Bioanalytical

Durham, NC · On-site

$17.25 - $23/hr

Position Summary The Lab Technician will support the bioanalytical laboratory by performing routine ... Quality Control Travel requirements: * 0-10% of job time. No expected travel on a routine basis.

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Quality Control Bioanalytical information

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How much do quality control bioanalytical jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for quality control bioanalytical in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Quality Control Bioanalytical specialist, and why are they important?

To thrive as a Quality Control Bioanalytical specialist, you typically need a background in life sciences or chemistry, experience with analytical techniques, and knowledge of regulatory standards such as GMP. Familiarity with laboratory instruments like HPLC, GC, and LIMS, as well as certifications in quality management, are highly valued. Attention to detail, strong problem-solving skills, and effective teamwork set outstanding professionals apart in this role. These qualifications ensure accurate data, compliance with industry regulations, and the delivery of safe, high-quality products.

What are some common challenges faced by professionals in Quality Control Bioanalytical roles, and how can they be addressed?

Professionals in Quality Control Bioanalytical roles often encounter challenges such as managing tight deadlines, ensuring compliance with strict regulatory standards, and troubleshooting complex analytical instrumentation. Effective communication with cross-functional teams, ongoing training on evolving technologies, and meticulous documentation are key to overcoming these challenges. Collaborating closely with R&D and production teams also helps ensure data integrity and timely resolution of issues, supporting both product quality and continuous improvement.

What is a Quality Control Bioanalytical professional?

A Quality Control Bioanalytical professional is responsible for ensuring the accuracy, reliability, and compliance of analytical testing in biopharmaceutical environments. They perform laboratory tests on biological samples to verify the quality and safety of products, following strict regulatory guidelines. Their work helps ensure that products meet required specifications before being released to the market. These professionals typically use advanced instruments and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

What is the difference between Quality Control Bioanalytical vs Quality Control Microbiological?

AspectQuality Control BioanalyticalQuality Control Microbiological
Required CredentialsBachelor's or higher in Life Sciences, relevant certificationsBachelor's or higher in Microbiology, relevant certifications
Work EnvironmentLaboratories focused on drug analysis, pharmacokineticsMicrobiology labs, contamination testing, sterilization validation
Industry UsagePharmaceutical, biotech, clinical researchPharmaceutical, food, cosmetics industries
Common Search/ComparisonYesYes

Quality Control Bioanalytical and Quality Control Microbiological roles both involve testing within the pharmaceutical industry but focus on different aspects. Bioanalytical QC emphasizes analyzing drug compounds and pharmacokinetics, while Microbiological QC concentrates on contamination control and sterilization processes. Both require relevant scientific credentials and are essential for ensuring product safety and efficacy in their respective fields.

Infographic showing various Quality Control Bioanalytical job openings in the United States as of May 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Principal Scientist, QC Analytical, Cell Therapy

Bristol Myers Squibb

Devens, MA • On-site

$124.59K - $150.98K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Subject matter expert in bioanalytical techniques leading method
transfer/validation and routine testing of in-process, final product, and
stability samples. Conceptualize and lead complex projects, CAPAs,
deviations, and continuous improvement efforts. Represent department
in product review boards, regulatory inspections, and author responses
to regulatory requests. Apply technical knowledge, regulatory
requirements, and scientific principles to independently perform
complex troubleshooting and problem solving.

Work Schedule:

Monday through Friday with weekend and holiday support if required but not routinely expected

Duties and responsibilities:

  • Subject matter expert in bioanalytical techniques (e.g., cell-based assays, ELISA, qPCR, flow cytometry) leading method transfer/validation and routine testing of in-process, final product, and stability samples.

  • SME for training and mentoring team on multiple complex QC test methods, processes, and procedures.

  • Independently develop, write, and execute methods, protocols, reports, and other related documents aligned with regulatory and corporate guidelines. Represent the department in product review boards, regulatory inspections (internal and external audits).

  • Own and author responses to regulatory requests.

  • Review and approve laboratory investigations.

  • Champion and foster a positive and successful collaborative quality culture. Conceptualize and lead complex projects, CAPAs, deviations, and continuous improvement efforts.

  • Own sections of APQR.

  • Represent QC interest on cross functional/ cross-site teams and communicate and collaborate effectively.

  • Apply technical knowledge, regulatory requirements, and scientific principles to perform troubleshooting and problem solving for nonroutine complex issues. Perform other tasks as assigned

Education and Experience:

Bachelor's degree or equivalent required, preferably in science. Advanced degree preferred. Netherlands: PhD in (bioanalytical) science preferred. Bachelor's degree in (bioanalytical) science with equivalent combination of work experience may be considered.

10+ years of relevant analytical testing, including 2+ years of QC experience, or an equivalent combination of education and experience.

Expert scientific knowledge with a broad range of bioanalytical techniques (cell-based assays, ELISA, qPCR, flow cytometry) and deep expertise with the characterization, validation, and transfer of bioanalytical methods.

Required Knowledge and skills:

Advanced ability to accurately and completely understand, follow, interpret and apply global regulatory and cGMP requirements.

Demonstrated advanced technical writing skills.

Advanced strategic thinking and problem-solving ability/mentality, technically adept and logical.

Ability to work independently in a fast-paced team environment, meet deadlines, and prioritize work from multiple projects.

Advanced ability to communicate and collaborate effectively with peers, senior management and cross-functional peers about task status, roadblocks and needs, locally and globally.

Advanced mentoring, coaching, influencing, negotiating and personnel interaction skills.

#LI-ONSITE

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Devens - MA - US: $124,590 - $150,977

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • Health Coverage: Medical, pharmacy, dental, and vision care.

  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1602048 : Principal Scientist, QC Analytical, Cell Therapy