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Quality Control Biochemistry Jobs (NOW HIRING)

WuXi Biologics

Scientist I, Quality Control

Cranbury, NJ · On-site

$60K - $960K/yr

Bachelor's degree in Analytical Chemistry, Biochemistry, or related field with a minimum of 4 years of industry quality control experience. * Or Master's degree in Analytical Chemistry, Biochemistry ...

GlaxoSmithKline

QC Scientist

King Of Prussia, PA · On-site

$60 - $80/hr

... using chemical, biochemical, and microbiological methods. - Prepare samples, standards, and ... Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing ...

GlaxoSmithKline

QC Scientist

King Of Prussia, PA · On-site

... using chemical, biochemical, and microbiological methods.- Prepare samples, standards, and ... Quality Control (QC), Risk Awareness, Testing Operations Please visit GSK US Benefits Summary to ...

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Sc. in Chemistry with concentration in Biochemistry Experience: 1-3 years in the field of Pharmaceutical (manufacturing facility). Background in the functional areas of Quality Control in Stability ...

H.B. Fuller

Quality Control Manager

South Bend, IN · On-site

$100 - $125/hr

The QC Manager plans and coordinates activities of the QC lab and is accountable for timely and ... Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry or Engineering * Minimum 5-10+ ...

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Quality Control Biochemistry information

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How much do quality control biochemistry jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality control biochemistry 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 quality control biochemistry?

Quality Control Biochemistry is a specialized field within the pharmaceutical, biotechnology, and food industries that focuses on testing and verifying the chemical and biological properties of products to ensure they meet required safety and quality standards. Professionals in this area use a variety of analytical techniques to assess the purity, potency, and stability of substances, such as drugs or food ingredients. Their work is essential for compliance with regulatory guidelines and helps prevent the release of unsafe or ineffective products to the market. Quality Control Biochemistry often involves collaboration with other departments, strict documentation, and adherence to Good Manufacturing Practices (GMP).

What are the key skills and qualifications needed to thrive as a quality control biochemistry specialist?

To thrive as a Quality Control Biochemistry Specialist, you need a strong background in biochemistry or a related life science, with experience in analytical techniques such as HPLC, ELISA, and spectrophotometry, often supported by a relevant bachelor's or master's degree. Familiarity with laboratory information management systems (LIMS), GMP/GLP regulations, and certifications like ASQ or similar are highly valued. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills in this role. These competencies ensure accurate testing, regulatory compliance, and the reliability of biopharmaceutical products.

What are some common challenges faced in a quality control biochemistry role, and how can they be addressed?

In a Quality Control Biochemistry role, professionals often encounter challenges such as tight testing deadlines, handling complex instrumentation, and ensuring compliance with rigorous regulatory standards. Working with sensitive biological samples requires strong attention to detail and the ability to quickly troubleshoot equipment or assay issues. Collaboration with cross-functional teams, such as manufacturing and regulatory affairs, is essential for resolving discrepancies and maintaining product quality. To address these challenges, staying current with standard operating procedures, participating in ongoing training, and fostering open communication within the team are highly effective strategies.

What is the difference between Quality Control Biochemistry vs Quality Control Microbiology?

AspectQuality Control BiochemistryQuality Control Microbiology
Required CredentialsBachelor's in Biochemistry, Chemistry, or related field; certifications like ASQ CQE often preferredBachelor's in Microbiology, Biology, or related; similar certifications valued
Work EnvironmentLaboratories focused on chemical and biochemical testing of raw materials, in-process, and finished productsLaboratories testing microbial contamination, sterility, and microbial counts in products
Employer & Industry UsagePharmaceutical, biotech, and chemical manufacturing companiesPharmaceutical, food, and beverage industries

Both roles involve quality testing but focus on different aspects: biochemistry emphasizes chemical analysis, while microbiology concentrates on microbial testing. Understanding these differences helps in choosing the right career path or job search focus within quality assurance roles.

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

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

Infographic showing various Quality Control Biochemistry job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Quality Control Supervisor

Middletown, VA • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

$75K - $113K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 430 frontline employees who took The Breakroom Quiz

171st of 547 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting

Job Description

Thermo Fisher Scientific’s Clinical Diagnostics Division supports diagnostic solutions that help healthcare professionals make informed clinical decisions. The Middletown, VA site operates within a highly regulated manufacturing environment where Quality Control plays an important role in ensuring products consistently meet established quality, safety, and regulatory requirements.

The QC Supervisor provides day-to-day leadership and oversight of Quality Control laboratory operations at the Middletown, VA site. This role leads laboratory personnel, coordinates testing priorities, and helps ensure accurate and timely testing in compliance with cGMP, site procedures, and applicable regulatory requirements.

Working cross-functionally with Quality Assurance, Manufacturing, Engineering, Validation, and other partners, the QC Supervisor supports product release, laboratory investigations, inspection readiness, and continuous improvement initiatives.

Location: Middletown, VA
Relocation: Relocation assistance is not available for this position.

Key Responsibilities
  • Supervise, coach, and develop QC laboratory personnel.
  • Coordinate daily testing priorities and laboratory workload.
  • Review and approve laboratory data and controlled documentation.
  • Support product release, environmental monitoring, and routine QC testing.
  • Lead or support OOS, OOT, deviation, and laboratory investigations.
  • Support CAPAs, change controls, and continuous improvement initiatives.
  • Ensure laboratory equipment, training, and documentation remain compliant.
  • Maintain inspection readiness and support internal and regulatory audits.
  • Monitor laboratory performance, turnaround time, and key quality metrics.
  • Partner with QA, Manufacturing, Engineering, Validation, and other departments.
Qualifications
  • Bachelor's degree in Chemistry, Biology, Microbiology, Biochemistry, or related scientific field.
  • 5+ years of QC laboratory experience in a regulated industry.
  • Previous supervisory or team leadership experience preferred.
  • Strong knowledge of cGMP, Good Documentation Practices, and data integrity.
  • Experience with laboratory investigations, deviations, CAPAs, and change controls.
  • Strong leadership, communication, organization, and problem-solving skills.
Preferred Experience
  • Pharmaceutical, biologics, diagnostics, or medical device manufacturing.
  • Environmental monitoring and microbiology testing.
  • LIMS, SAP, MasterControl, or similar quality/laboratory systems.
  • Lean or continuous improvement methodologies.

Compensation and Benefits

The salary range estimated for this position based in Virginia is $75,800.00–$113,675.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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