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Quality Control Bioanalytical Jobs (NOW HIRING)

MSD

Director, Bioanalytical Laboratory

Gaithersburg, MD · On-site

$114K - $149K/yr

... quality control and safety requirements. • Ensures laboratory procedures, methods and staff ... bioanalytical sample testing in a GLP/GCLP environment is required. • A minimum of 6 years of ...

Iff

Senior Scientist, Bioanalytics

Wilmington, DE · On-site

$88K - $121K/yr

Provide advanced technical leadership within the Global Bioanalytical Quality Technical function through strong expertise in statistical quality control (SQC), analytical method performance, and data ...

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Quality Control Bioanalytical information

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How much do quality control bioanalytical jobs pay per hour?

As of Sep 9, 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 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 are the key skills and qualifications needed to thrive as a quality control bioanalytical specialist?

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 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.

What states have the most Quality Control Bioanalytical jobs?

States with the most job openings for Quality Control Bioanalytical jobs include:

What are popular job titles related to Quality Control Bioanalytical jobs?

For Quality Control Bioanalytical jobs, the most frequently searched job titles are:

Infographic showing various Quality Control Bioanalytical job openings in the United States as of June 2026, with employment types broken down into 94% Full Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Senior Scientist, Bioanalytical Sciences (Cambridge, MA)

Cambridge, MA • On-site

Cedent
IT Services • 11 - 50 employees
Learn more about Cedentexternal

$100K - $136K/yr

Full-time

Re-posted 7 days ago

Job description

The client is seeking an experienced Senior Scientist to join their Bioanalytical Sciences team. In this hands-on, lab-based role, you will lead the design, development, and execution of regulatory-aligned bioanalytical assays supporting IND-enabling studies for our mRNA-LNP therapeutics. You will be a subject matter expert in nucleic acid and protein bioanalysis, working to generate critical data that informs decision-making across preclinical and clinical development. You will be instrumental in building client's IND readiness and advancing our genetic medicine platform. You will report into the VP, Head of DMPK and Clinical Pharmacology, with the expectation to be onsite 5 days a week. This is an individual contributor role.
You will:
  • Design and execute phase-appropriate bioanalytical strategies for mRNA-based delivery systems
  • Develop, optimize, and qualify RT-qPCR-based assays for quantifying LNP-delivered mRNA in biological matrices
  • Develop and oversee ligand-binding immunoassays (ELISA, MSD, Luminex or similar platforms) for the detection of translated proteins and anti-drug or anti-protein antibodies, including screening, confirmatory, and neutralizing antibody assays in accordance with regulatory guidance
  • Collaborate with stakeholders in DMPK, Toxicology, Clinical, and Regulatory to ensure assay readiness, study support, data integrity, and reporting across GLP and non-GLP studies
  • Become a bioanalytical SME for external CROs to ensure method transfer, scientific rigor, compliance, and execution of assay development, sample analysis, and method validation/qualification
  • Review, interpret, and present bioanalytical data to teams; contribute to the authorship of study reports, assay qualification/validation summaries, and regulatory documentation (e.g., IND Module 4/5)
  • Ensure all analytical work is conducted in alignment with regulatory expectations and fit-for-purpose principles
  • Stay current on emerging technologies and industry standards in nucleic acid and protein bioanalysis.
Qualifications:
  • Ph.D. in Biochemistry, Molecular Biology, Pharmaceutical Sciences, or a related field with a minimum of 5 years of industry experience; an M.S. with 8+ years of relevant industry experience will also be considered
  • Prior contribution to IND submissions or regulatory responses related to bioanalysis
  • Experience with nucleic acid bioanalysis using RT-qPCR for quantifying mRNA or oligonucleotides in preclinical or clinical settings
  • Experience developing and qualifying ligand-binding assays (ELISA, MSD, Luminex) for protein quantification and ADA characterization
  • Experience managing outsourced bioanalytical work, including CRO oversight, protocol review, and data quality control
  • Familiarity with regulatory guidance (e.g., ICH M10) and FDA/EMA expectations for bioanalytical support of IND submissions
  • Experience with data interpretation
  • Commitment to our Core Values: Respect, Integrity, Excellence, and Impact
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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