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Overnight Biotech Quality Control Jobs (NOW HIRING)

Astrix Inc

Quality Control Scientist

Vista, CA · On-site

$47/hr

We are seeking a Quality Control Scientist to join the Raw Materials team supporting a global pharmaceutical/biotech organization. This is a great opportunity to gain hands-on experience in a GMP ...

Legend Biotech USA, Inc.

$83.71K - $109.87K/yr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... The QC Specialist is encouraged to work independently on routine tasks and have conceptual ...

Pacer Group

Quality Control Specialist

San Diego, CA · On-site

... a biotech lab environment. The QC Associate I is responsible for routine, accurate and timely ... testing of QC samples according to standard protocols and operating procedures, such as flow ...

NWRPros

Director, Quality Control, CMC

Seattle, WA · On-site

Experience in big pharma/biotech; experience in a startup biopharma company is desirable ... Occasionally required to travel overnight * Ability to travel 10% of the time Supervisory ...

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 ...

Tunnell Consulting

Quality Control Manager

Raleigh, NC · On-site

... biotech, pharma, the U.S. Government, foundations, public/private partnerships, investors, and ... Our client is seeking a Quality Control (QC) Manager to lead both Microbiology and Analytical ...

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 ...

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 . Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing QC ...

Legend Biotech US

QC Analyst II

Raritan, NJ · On-site

$24.50 - $33/hr

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

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 ...

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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 May 30, 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 are the key skills and qualifications needed to thrive as an Overnight Biotech Quality Control professional, and why are they important?

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 are Overnight Biotech Quality Control jobs?

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 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.

More about Overnight Biotech Quality Control jobs
What cities are hiring for Overnight Biotech Quality Control jobs? Cities with the most Overnight 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 Overnight Biotech Quality Control jobs? States with the most job openings for Overnight Biotech Quality Control jobs include:
What job categories do people searching Overnight Biotech Quality Control jobs look for? The top searched job categories for Overnight Biotech Quality Control jobs are:
Overnight Biotech Quality Control jobs near you
Infographic showing various Overnight Biotech Quality Control job openings in the United States as of May 2026, with employment types broken down into 65% Full Time, 31% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 3% Hybrid, and 1% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
Quality Control Scientist

Quality Control Scientist

Astrix Inc

Vista, CA • On-site

$47/hr

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking a Quality Control Scientist to join the Raw Materials team supporting a global pharmaceutical/biotech organization. This is a great opportunity to gain hands-on experience in a GMP environment with strong potential for long-term growth and conversion.
Location: San Diego County, CA (Onsite)
Pay Rate: $36-$47/hr (based on experience)
Schedule: Monday - Friday, 8:00 AM Start
6-Month Contract ( potential for conversion)
Pay Rates:
(1-3 years): Up to $36/hr
(3-5 years): Up to $40/hr
(5+ years): Up to $47/hr
Key Responsibilities
  • Perform QC testing on raw materials, in-process samples, and finished products
  • Conduct analytical testing and review data for accuracy and completeness
  • Maintain compliance with cGMP standards, SOPs, and documentation practices
  • Write, revise, and support GMP documentation (SOPs, specifications, test methods)
  • Operate and maintain analytical instrumentation (HPLC, UPLC, GC, Mass Spec, UV)
  • Support method validation, calibration, and equipment maintenance
  • Manage raw material processes including receiving, quarantine, testing, and release
  • Investigate deviations, out-of-specification results, and support stability activities

Qualifications
  • Bachelor's degree in Chemistry or related field (Master's preferred)
  • Minimum 1+ year of experience in a GMP pharma/biotech environment
  • Hands-on experience with HPLC (required)
  • Experience with analytical instrumentation (GC, HPLC, Mass Spec, etc.)
  • Experience in QC, raw materials, or analytical lab settings
  • Strong understanding of GMP and documentation practices

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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