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Overnight Quality Assurance Biotech Jobs (NOW HIRING)

Kelly Services

Overnight QA Supervisor

Lancaster, SC

$75K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Initial training will be completed on 1st Shift Salary: $75,000-$85,000 + Annual Bonus Opportunity We are seeking a Quality Assurance Supervisor to lead our overnight QA team in a fast-paced, FDA ...

SpecialtyRX

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Overnight QA Wellness Rep

Ridgefield Park, NJ · On-site

$19 - $22/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We're currently seeking Full Time Overnight Wellness Quality Assurance Rep to join our New Jersey Team. Wellness Quality Assurance Rep: we offer competitive salary and benefit package. Hours: 7:00pm ...

Legend Biotech US

QA Investigations Lead II

Raritan, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role Overview The QA Investigation Lead is an exempt level position reporting to the QA ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

  • Medical

  • Retirement

  • PTO

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Chamblee, GA

  • Medical

  • Retirement

  • PTO

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Chamblee, GA · On-site

  • Medical

  • Retirement

  • PTO

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

  • Medical

  • Retirement

  • PTO

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Alpharetta, GA

  • Medical

  • Retirement

  • PTO

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

Actalent

Quality Assurance Technician

Cambridge, MA · On-site

$30 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role works closely with the QA team to maintain accurate documentation, manage Trackwise entries, and support a growing product line within a regulated pharmaceutical or biotech environment.

Legend Biotech USA, Inc.

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe QA Investigation Lead is an exempt level position reporting to the QA ...

Kinetic Personnel Group

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Quality Assurance Biopharma

Tustin, CA · On-site

$25 - $37.50/hr

Bachelor's degree in Biology, Biotechnology, Biochemistry, Chemistry, Pharmaceutical Sciences, or a related Life Sciences field preferred. * 1-3 years of experience in Quality Assurance, Quality ...

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Overnight Quality Assurance Biotech information

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$13

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

As of Aug 18, 2026, the average hourly pay for overnight quality assurance biotech in the United States is $31.24, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $36.54 per hour, depending on experience, location, and employer.

What does an overnight quality assurance biotech do?

An Overnight Quality Assurance Biotech is responsible for monitoring and maintaining the quality of biotech products and processes during nighttime or overnight shifts. They conduct inspections, review documentation, perform audits, and ensure that manufacturing operations comply with regulatory standards and company protocols. This role is crucial for continuous production environments, as it helps prevent errors, ensures product safety, and addresses any quality issues that arise outside of regular business hours.

What are the key skills and qualifications needed to thrive as an overnight quality assurance biotech, and why are they important?

To thrive as an Overnight Quality Assurance Biotech, you need a solid background in biology or chemistry, familiarity with GMP/GLP regulations, and a relevant degree or certification in life sciences. Experience with laboratory equipment, LIMS (Laboratory Information Management Systems), and quality management software is typically required. Strong attention to detail, effective communication, and problem-solving skills are essential soft skills for this role. These skills and qualities ensure that quality standards are consistently met during off-hours, maintaining compliance and product integrity in a 24/7 biotech environment.

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

Overnight Quality Assurance Biotech professionals often encounter challenges such as limited immediate access to senior staff, managing time-sensitive quality issues, and maintaining focus during off-hours. To effectively manage these challenges, professionals should develop strong communication with day teams, utilize thorough documentation practices, and stay organized to ensure smooth handovers. Additionally, fostering self-motivation and building a reliable support network with other overnight team members can help maintain high-quality standards throughout the shift.

What is the difference between Overnight Quality Assurance Biotech vs Quality Control Technician?

AspectOvernight Quality Assurance BiotechQuality Control Technician
CertificationsGMP, ISO, QA certificationsGMP, ISO, Lab certifications
Work EnvironmentBiotech manufacturing, labs, overnight shiftsLaboratories, manufacturing plants, shifts vary
Job FocusProcess compliance, documentation, auditsTesting, sample analysis, data recording

Overnight Quality Assurance Biotech professionals focus on ensuring manufacturing processes meet quality standards through audits and documentation, often working overnight shifts in biotech facilities. In contrast, Quality Control Technicians primarily perform testing and analysis of samples to verify product quality. While both roles require GMP knowledge and similar certifications, their daily tasks and focus areas differ, with QA emphasizing process oversight and QC concentrating on testing procedures.

More about Overnight Quality Assurance Biotech jobs

What cities are hiring for Overnight Quality Assurance Biotech jobs?

Cities with the most Overnight Quality Assurance Biotech job openings:

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

The most popular types of Quality Assurance Biotech jobs are:

What states have the most Overnight Quality Assurance Biotech jobs?

States with the most job openings for Overnight Quality Assurance Biotech jobs include:

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The top searched job categories for Overnight Quality Assurance Biotech jobs are:

Overnight Quality Assurance Biotech jobs near you
Infographic showing various Overnight Quality Assurance Biotech 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 $64,986 per year, or $31.2 per hour.

Overnight QA Supervisor

Kelly Services

Lancaster, SC

$75K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago

Job description

Quality Assurance Supervisor – 3rd Shift

Location: Lancaster, SC
Shift: Sunday – Thursday | 11:15 PM – 7:15 AM
Training: Initial training will be completed on 1st Shift
Salary: $75,000–$85,000 + Annual Bonus Opportunity

We are seeking a Quality Assurance Supervisor to lead our overnight QA team in a fast-paced, FDA-regulated manufacturing environment. This role is responsible for overseeing Quality Assurance personnel, ensuring compliance with cGMP and company quality standards, supporting manufacturing operations, and driving continuous improvement initiatives. We're looking for a hands-on leader who can coach and develop employees while maintaining a strong culture of quality and accountability.

What You'll Do
  • Supervise, coach, and develop Quality Assurance personnel on 3rd shift.
  • Provide QA oversight for manufacturing, packaging, and warehouse operations.
  • Review batch records, production documentation, and quality records for accuracy and compliance.
  • Lead investigations involving deviations, non-conformances, and quality events while driving effective CAPA implementation.
  • Partner with Manufacturing, Quality Control, and cross-functional teams to resolve quality issues and improve processes.
  • Ensure compliance with FDA regulations, cGMP requirements, SOPs, and company quality standards.
  • Support internal audits, regulatory inspections, and inspection readiness activities.
  • Train employees on GMP requirements, quality systems, and standard operating procedures.
  • Monitor quality metrics and champion continuous improvement initiatives throughout the department.
Required Qualifications
  • Associate's or Bachelor's degree in a science-related field preferred.
  • 4–5+ years of experience in an FDA-regulated manufacturing or production environment.
  • At least 3 years of Quality Assurance experience.
  • Experience with:
    • FDA and cGMP regulations
    • SOPs
    • Batch record review
    • Deviations and non-conformances
    • ISO standards
    • Lean Manufacturing principles
    • Dietary supplement manufacturing (preferred)
  • Proven leadership experience managing teams, including:
    • Coaching and mentoring employees
    • Holding team members accountable
    • Managing difficult conversations
    • Conflict resolution
    • Ensuring policy compliance
  • Strong communication, organizational, and problem-solving skills.
  • Passion for continuous improvement and driving positive change within Quality Operations.
Compensation & Benefits
  • Salary: $75,000–$85,000, based on experience.
  • Annual Bonus: Eligible to earn up to 15% of year-to-date earnings. While not guaranteed, bonuses are typically paid during Q1 of the following year.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.