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Day Biotech Quality Control Jobs (NOW HIRING)

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Astrix Inc

QC Analyst

Chapel Hill, NC · On-site

$33.65 - $36.06/hr

Bachelor's degree in Biology, Microbiology, Biochemistry, Biotechnology, Chemistry, or another related life science field OR * 3+ years of relevant Quality Control, Analytical Development, GMP, or ...

Adecco

Quality Control Analyst

Plainville, MA · On-site

$23.50 - $31.50/hr

Adecco Healthcare & Life Sciences is hiring for a leading global pharmaceutical and biotechnology ... QC Microbiology Analyst I Location: Onsite Schedule: Sunday - Wednesday | 11:00 AM - 9:30 PM (30 ...

Genentech

Quality Control Associate II

Oceanside, CA · On-site

$66K - $110K/yr

You possess a Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline with 5-6 years of experience in pharmaceutical/biotech QC labs, including hands-on raw material testing ...

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

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

BioLegend

Quality Control Supervisor

San Diego, CA

Oversee the day to day operations of the Flow QC group, including assigning testing samples to QC ... 6 years of biotech industry experience related to Quality Control * 2 years of experience ...

Actalent

Quality Control Technician

Richmond, CA

$27 - $33/hr

Experience in the medical device or biotechnology industry with a technical background is preferred ... days per week. Work takes place in a controlled manufacturing or sterilization environment that ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

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 ...

Precigen, Inc

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 ...

Legend Biotech US

Sr. QC Analyst

Raritan, NJ

$24.50 - $33/hr

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ . Shift: 3rd shift Wed-Sat Role Overview The Sr. QC Analyst is an exempt level position with ...

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product quality in a biotech environment. This role is essential to maintaining compliance and product ...

Omeros

Director, Quality Control

Seattle, WA

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 ...

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

As of Jun 29, 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:
Day Biotech Quality Control jobs near you
Quality Control Specialist

Quality Control Specialist

TekWissen LLC

Vacaville, CA • On-site

$20 - $26/hr

Contractor

Posted 24 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 Specialist II 
Location:      Vacaville, CA, 95688 
Duration:      6 Months    
Job Type:      Temporary Assignment 
Work Type:  Onsite 
Shift:             Monday to Friday from 08:00 AM to 04:00 PM
 
Summary: 
  • Under moderate supervision, the QC Specialist supports planning, managing, and executing projects related to the product portfolio for Vacaville Quality Control.
  • These projects include analytical transfers, control system updates, regulatory filings, and other product life-cycle activities.
  • The individual partners with customers across the site and with other locations to meet project objectives.
  • Additionally, they contribute to developing and improving processes and procedures related to Quality Control activities.
  • This position plays a critical role in new product and/or technology transfers within the Vacaville Quality Control organization.
Responsibilities: 
  • Assist in managing projects and technical activities associated with method improvements, method transfers, and lab-related activities.
  • Support project teams to meet schedules, timelines, and deadlines.
  • Collaborate with internal departments, external partners, and customers to support multi-site operational activities.
  • Ensure GMP compliance throughout operations.
  • Participate in project teamwork, process improvements, and group initiatives.
  • Achieve scheduled performance targets (e.g., 95% on-time delivery).
  • Assist in execution of projects such as method transfers and method validations.
  • Support activities related to products, control systems, and health authority filings.
  • Monitor analytical methods, manage reference material replenishment and testing.
  • Identify and resolve discrepancies as applicable.
Required Skills: 
  • BS/BA degree with 2–3 years of commercial quality control experience (pharmaceutical/biopharmaceutical preferred).
  • Strong knowledge of GMP quality control systems.
  • Experience in a relevant scientific discipline.
  • Strong planning skills for working with cross-functional teams.
  • Ability to negotiate, influence, and make decisions to meet objectives.
  • Excellent verbal and written communication skills with the ability to present formally and informally.
  • Solid understanding of scientific theories, principles, and techniques used in analytical and/or biological test procedures.
  • Demonstrated judgment, reasoning, and problem-solving skills.
  • Ability to work with moderate independence or under supervision while managing multiple projects.
Desired Skills
  • Prior experience in pharmaceutical or biopharmaceutical quality control operations.
  • Experience with analytical method transfers and validations.
  • Familiarity with regulatory filings and product life-cycle management.
  • Demonstrated ability to contribute to process improvements within QC operations.
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. 

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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

Social media

Twitter

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