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Overnight Biotech Quality Control Jobs (NOW HIRING)

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

Quality Control Technician Poly-America, L.P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags ...

Legend Biotech US

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC ...

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

Quality Control Technician Poly-America, L.P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags ...

BioPhase Solutions

QC Inspector

San Diego, CA · On-site

$18 - $19.80/hr

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

LegendBiotech

WI · On-site

$23.25 - $31.25/hr

As a QC analyst, you will play a critical role in ensuring the highest quality of life-saving cell ... Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting ...

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags, construction and agricultural films. Quality ...

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags, construction and agricultural films.

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe QC Analyst is an exempt level position with responsibilities for performing QC ...

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags, construction and agricultural films.

Legend Biotech USA

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is seeking a QC Analyst as part of the Quality Operations team based in Raritan, NJ. Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC ...

Legend Biotech USA, Inc.

$63K - $83K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... The QC Specialist is encouraged to work independently on routine tasks and have conceptual ...

Thorne

Quality Control Supervisor

Summerville, SC · On-site

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

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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 Sep 10, 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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For Overnight Biotech Quality Control jobs, the most frequently searched job titles are:

Overnight Biotech Quality Control jobs near you
Infographic showing various Overnight Biotech Quality Control job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Senior Manager, Quality Control

San Francisco, CA • On-site

Vir Biotechnology
Biotechnology Research and Development • 51 - 200 employees
Learn more about Vir Biotechnologyexternal

$142K - $199K/yr

Full-time

Medical, Retirement, PTO

Re-posted 15 days ago

Key responsibilities

  • Execute and operationalize QC strategy for assigned programs and external testing networks.

  • Manage day-to-day QC operations, including overseeing release and stability testing, review of analytical data, and supporting documentation.

  • Coordinate and oversee vendor performance, external lab activities, and method lifecycle activities.

Job description

THE OPPORTUNITY

The Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. This role ensures the timely and compliant delivery of QC activities, including release and stability testing, method lifecycle management, and vendor oversight. 

The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions. This individual contributes to the development of QC strategy and drives continuous improvement in QC processes, systems, and external network performance. 

This role is located in our San Francisco headquarters with an expectation of 3 days per week in office.

WHAT YOU'LL DO
  • Execute and operationalize QC strategy for assigned programs and external testing networks in alignment with QC and Quality organization strategy.  
  • Lead QC activities across the product lifecycle (Phase 1 through commercial) for designated programs, ensuring effective implementation of phase-appropriate control strategies.  
  • Support development and refinement of QC strategies, including methods, specifications, and testing approaches, in collaboration with Analytical Development and QC leadership.  
  • Drive consistent execution and harmonization of QC methods, specifications, and practices across programs and external partners.  
  •  Identify, assess, and escalate risks to QC performance, supply continuity, and compliance, and implement mitigation plans with cross-functional stakeholders. 
  • Represent QC on program teams and sub-teams, ensuring alignment of analytical deliverables, timelines, and QC readiness for key CMC milestones. 
  • Manage day-to-day execution of QC operations to ensure timely, compliant testing for clinical and commercial programs.  
  • Coordinate and oversee release and stability testing (including CDMOs/CTLs), including review of analytical data, batch records, and supporting documentation; support CoA generation.  
  • Lead execution of QC GMP processes (deviations, OOS/OOT, change controls, investigations) in collaboration with QA.  
  • Coordinate QC documentation and logistics at external labs, including sampling plans, shipments, and reagent/inventory management.  
  • Manage vendor performance and execution, including CTL/CDMO oversight and routine operational interactions.  
  • Execute method lifecycle activities (qualification, transfer, validation, implementation, and monitoring) across internal and external labs.  
WHO YOU ARE AND WHAT YOU BRING
  • BA/BS with 10 + years experience, MA/MS/MBA with 8+ years experience in Biochemistry, Chemistry, Biology, Virology, Chemical Engineering or a related discipline is preferred
  • Technical expertise in a wide range of analytical methods for release and stability testing of monoclonal antibodies
  • Strong scientific background in Quality Control and/or assay development in biotech industry with strong knowledge of cGMP/ICH/FDA/EMA regulations
  • Expertise with analytical test method optimization, validation, and transfer as well as working with contract organizations 
#LI-AS1
#LI-Onsite
 
WHO WE ARE AND WHAT WE OFFER

The expected salary range for this position is $142,500 to $199,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.

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