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Overnight Biotech Quality Control Jobs (NOW HIRING)

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 ...

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 ...

QC, Analyst I

Raritan, NJ · On-site

$68.04 - $95.54/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in ...

New

QC, Analyst I

Raritan, NJ · On-site

$68.04 - $95.54/hr

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing ... Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in ...

New

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 ...

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 ...

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 ...

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

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 · On-site

$41K - $66K/yr

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 ...

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 ...

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 ...

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 ...

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Overnight Biotech Quality Control information

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

As of Aug 20, 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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What are the most commonly searched types of Biotech Quality Control jobs?

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What job categories do people searching Overnight Biotech Quality Control jobs look for?

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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, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

cGMP Quality Control (QC) Specialist

Keck Medicine of USC

Los Angeles, CA

$87K - $92K/yr

Full-time

Re-posted 25 days ago


Keck Medicine of USC rating

7.5

Company rating: 7.5 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

301st of 1,060 rated hospitals


Job description

The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the "Trojan Family," which is comprised of the faculty, students and staff that make the university what it is.

USC's Keck School of Medicine, Department of Medicine is seeking a dynamic individual to work on the manufacturing of biologics and drugs for cell and gene therapy of internal/external users in the university's current Good Manufacturing Practices (cGMP) facility. The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and implementing quality control testing, assays, and procedures for materials and final cell therapy products manufacturing. The position will also be responsible for ensuring consistency with current Good Manufacturing Practice (cGMP) principles.

Job Accountabilities:

  • Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible quality before being applied to patients. Writes and reviews qualifications (e.g., installation, operation, performance), facility operation plans and reports, standard operating procedures, and batch records as required. Completes batch record documentation, all appropriate equipment log entries, and cGMP documentation.
  • Operates instrumentation needed for cell and gene therapy manufacturing (e.g., cell counters, bioreactors, centrifuges, biological safety cabinets). Assists in technology transfer of manufacturing processes from pre-clinical into cGMP environment.
  • Provides verification of facility operations and equipment, along with advanced problem-solving, troubleshooting, and consultation support, as needed. Supervises and directs junior staff to achieve project goals. Serves as a resource to cGMP facility management in identifying and assessing the appropriate complement of resources and support needed to successfully implement and execute projects.
  • Maintains confidentiality for patient identification, specimen labeling, and specimen verification during batch testing. Performs duties in a clean room environment, when needed and while fully gowned (e.g., mask, coverall, gloves), following cGMP guidelines and using aseptic techniques. Works with senior staff to ensure facilities' compliance with all applicable regulations.
  • Attends routine meetings with the management team for progress reports on projects, facility needs, and discussion of any other required items. Improves current methods and evaluates innovative techniques in quality control testing for cell therapy and biologics.
  • Promotes an environment that fosters inclusive relationships and creates unbiased opportunities for contributions through ideas, words, and actions that uphold principles of the USC Code of Ethics.
  • Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.

Successful Candidates Must Demonstrate:

  • Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of all aspects of biotechnology and cell therapy. Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Extensive leadership experience.

Salary Range:

The annual base salary range for this position is $87,576.76 - $92,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

*This is a 3-year fixed-term position.

USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.

Minimum Education: Bachelor's degree
Minimum Experience: 3 years
Supervises: May lead one or more employees performing similar work
Minimum Field of Expertise: Bachelor's degree in a scientific discipline (e.g., pharmaceutical, biologics). Three years' experience in cellular or biological manufacturing with quality control responsibilities. Demonstrated knowledge base with Good Manufacturing Practices (e.g., cGMPs, GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work as an individual contributor and in a dynamic team environment. Excellent written and oral communication skills.
Preferred Education: Master's Degree
Preferred Experience: 5 Years
Preferred Field of Expertise: Biotechnology and life sciences

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to theBackground Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email atuschr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.

  • Notice of Non-discrimination
  • Employment Equity
  • Read USC's Clery Act Annual Security Report
  • USC is a smoke-free environment
  • Digital Accessibility

If you are a current USC employee, please apply to this  USC job posting in Workday by copying and pasting this link into your browser:

https://wd5.myworkday.com/usc/d/inst/1$9925/9925$125114.htmld

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