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Qc Biotech Jobs (NOW HIRING)

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, master's degree in ...

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

... in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of ... QC laboratory. Alternatively, master's degree in above areas with 8 years of experience in a ...

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A-Line Staffing is now hiring a Quality Control Microbiologist in El Paso, TX. The Quality Control Microbiologist would be working for a Fortune 500 BioTech company and has career growth potential.

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

QC Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

... biotech QC laboratory. Experience: • Previous experience in a cGMP laboratory. • Strong ... background in small molecule and protein chemistry and experience troubleshooting analytical ...

... in a biotech lab environment. * The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow ...

... in a biotech lab environment. * The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow ...

QC Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in ...

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Qc Biotech information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc biotech jobs pay per year?

As of Jun 1, 2026, the average yearly pay for qc biotech in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QC Biotech, and why are they important?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.

What is a QC Biotech professional?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

More about Qc Biotech jobs
What cities are hiring for Qc Biotech jobs? Cities with the most Qc Biotech job openings:
What are the most commonly searched types of Qc Biotech jobs? The most popular types of Qc Biotech jobs are:
What states have the most Qc Biotech jobs? States with the most job openings for Qc Biotech jobs include:
Infographic showing various Qc Biotech job openings in the United States as of May 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Quality Control Manager

Quality Control Manager

Pinnaql

High Point, NC

Other

Posted 18 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Quality Control Manager

Summary:

We are seeking a Quality Control Manager for a 6 month contract to oversee laboratory operations and QC activities supporting pharmaceutical manufacturing processes. This is an onsite position in High Point, NC and local candidates are strongly preferred.

Responsibilities:

  • Manage QC laboratory operations including analytical and microbiological testing.
  • Ensure compliance with cGMP and data integrity requirements.
  • Review and approve laboratory investigations, OOS/OOT results, and CAPAs.
  • Support method validation, transfer, and stability programs.
  • Coordinate laboratory scheduling and resource planning.
  • Support audits and regulatory inspections.
  • Develop and mentor QC staff.

Qualifications:

  • Bachelors degree in Chemistry, Microbiology, or related scientific discipline.
  • 7+ years of QC laboratory experience in pharmaceutical manufacturing.
  • Prior supervisory or management experience.
  • Strong understanding of FDA and cGMP requirements.
  • Experience with analytical instrumentation and laboratory systems.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.