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Day Biotech Quality Control Jobs (NOW HIRING)

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

... and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in ...

QC Inspector

Bothell, WA

$41K - $66K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

QC Inspector

Bothell, WA

$41K - $66K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

QC Inspector

Bothell, WA

$37K - $66K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Minimum Education: Bachelor's degree in a related field strongly ...

Director, Quality Control

Seattle, WA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Director, Quality Control

Seattle, WA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 Inspector

Bothell, WA · On-site

$37K - $66K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

... biotechnology and medical devices. This means we have the resources to support you within this ... quality control specifications Set up instruments and conduct sample tests; utilize a variety of ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

QC Microbiologist

Seminole, FL · On-site

$85K - $87K/yr

Quality Control Microbiology Supervisor Overview: Quality Control (QC) Microbiology Supervisor ... Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory ...

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

Associate Director, Quality Control

Waltham, MA · On-site

$160 - $200/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

You will report directly to the head of QC and will serve as key contributor in overseeing day-to ... This role is based in Waltham, MA and you must have experience in biotech. Responsibilities

Specialist QC

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Showing results 41-60

Day Biotech Quality Control information

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How much do day biotech quality control jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for day biotech quality control 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 the difference between Day Biotech Quality Control vs Day Biotech Quality Assurance?

AspectDay Biotech Quality ControlDay Biotech Quality Assurance
Primary FocusTesting and inspecting products to ensure quality standards are met
ResponsibilitiesConducting lab tests, analyzing samples, documenting results
Work EnvironmentLaboratories, manufacturing facilities
CertificationsRelevant lab certifications, GMP training

Day Biotech Quality Control professionals focus on testing products to verify quality, while Day Biotech Quality Assurance staff develop and maintain processes to prevent defects. Both roles are essential in biotech manufacturing, often working closely but with distinct responsibilities.

What cities are hiring for Day Biotech Quality Control jobs?

Cities with the most Day Biotech Quality Control job openings:

What are the most commonly searched types of Biotech Quality Control jobs?

The most popular types of Biotech Quality Control jobs are:

What states have the most Day Biotech Quality Control jobs?

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

Quality Control Analyst

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Contractor

Re-posted 29 days ago


Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       QC Associate / Quality Control Analyst I
Location:       Vacaville, CA - 95688
Duration:       6 Months
Job Type:       Temporary Assignment     
Work Type:   Onsite

Summary
 
With limited supervision, the QC Associate I is responsible for performing direct materials testing in compliance with cGMP regulations. The role involves executing laboratory testing, reviewing and trending data, supporting investigations (OOS, OOT, OOE), and contributing to laboratory operations and quality objectives. The position works closely with Quality Control leadership to meet departmental and organizational goals.

Responsibilities

  • Perform basic to moderately complex laboratory testing in compliance with GMP requirements
  • Review, analyze, and assess test data against established acceptance criteria
  • Conduct technical review of peer-generated data
  • Perform trend analysis and assist in establishing limits
  • Identify discrepancies and support quality investigations and CAPA initiatives
  • Troubleshoot technical and testing-related issues
  • Identify gaps in systems, procedures, and laboratory practices
  • Participate in assay transfer, assay validation, and method-related activities
  • Perform equipment qualification, calibration, and routine maintenance
  • Prepare and maintain standards, controls, stocks, cultures, and reagents per procedures
  • Ensure GMP compliance across laboratory operations
  • Support internal and external audits and regulatory inspections
  • Coordinate with internal customers to support multi-site operations
  • Meet assigned schedules, timelines, and deadlines (95% on-time performance expectation)
  • Participate in or lead team projects, process improvements, and continuous improvement initiatives
  • Write protocols, reports, and technical documentation under limited supervision
  • Provide and receive training as required
  • Perform additional duties as assigned to support Quality activities
Required Skills
  • Bachelor’s degree (B.S./B.A.) in a relevant scientific discipline with 1–3 years of industry experience OR
  • Master’s degree with at least 1 year of relevant experience
  • Experience in the pharmaceutical or biopharmaceutical industry
  • Hands-on experience with analytical and/or biological testing procedures
  • Strong understanding of cGMP regulations and quality systems
  • Experience with OOS, OOT, and OOE investigations
  • Exposure to assay transfer, assay validation, and method lifecycle activities
  • Experience supporting regulatory inspections (FDA, EMA, etc.)
  • Familiarity with trend analysis and data integrity practices
  • Prior involvement in process improvement or cross-functional projects
  • Experience working in multi-site or global operational environments
  • Ability to apply scientific principles, theories, and techniques in a QC environment
  • Strong verbal and written communication skills
  • Sound judgment, analytical thinking, and problem-solving abilities
  • Ability to work independently with limited supervision and manage short-term priorities
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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