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Overnight Biotech Quality Control Jobs (NOW HIRING)

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 ...

Quality Control Scientist

Vista, CA · On-site

$41 - $91/hr

A brief overview The Quality Control Scientist performs laboratory day-today operations, guides and ... Minimum of 3 years' experience in GMP pharma/biotech facility * Experience with Equipment ...

New

Quality Control Scientist

Vista, CA · On-site

$62 - $138/hr

A brief overview The Quality Control Scientist performs laboratory day-today operations, guides and ... Minimum of 3 years' experience in GMP pharma/biotech facility * Experience with Equipment ...

Has experience in regulated manufacturing (strong preference: dietary supplements, pharma, biotech ... Comfortable working weekend overnight shift (3rd shift) * Strong communication and ability to hold ...

Has experience in regulated manufacturing (strong preference: dietary supplements, pharma, biotech ... Comfortable working weekend overnight shift (3rd shift) * Strong communication and ability to hold ...

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 ...

Manager, Quality Control Chemistry

Hopewell, VA · On-site

$110.80 - $150.80/hr

Manages all Quality Control (QC) Chemistry Laboratory - Capillary Electrophoresis (CE) activities ... Bachelor's degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or related ...

New

AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience OR * High School Degree and 3+ years' experience in biotechnology or related field and Quality ...

The job opportunity below is with one of our clients specializing in biotechnology product ... Quality Control Scientist Location: Eugene OR 97402 Duration: 4 Months Job Type: Temporary ...

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 ...

Manager, Quality Control

Germantown, MD · On-site

$105K - $140K/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 ...

Background in biotechnology, biopharmaceutical manufacturing, or QC laboratory environments. * Familiarity with GMP, GLP, HACCP, or food safety practices and their application in laboratory or ...

Showing results 41-60

Overnight Biotech Quality Control information

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

As of Sep 3, 2026, the average hourly pay for overnight 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 an overnight biotech quality control?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What are the key skills and qualifications needed to thrive as an overnight biotech quality control professional?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.

What are some common challenges faced by overnight biotech quality control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What is the difference between Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

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Infographic showing various Overnight Biotech Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% 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.

Quality Control Specialist

TekWissen LLC

Vacaville, CA • On-site

$20 - $26/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 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

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