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Weekend Biotech Quality Control Jobs (NOW HIRING)

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 ...

Astrix Inc

QC Supervisor- Night Shift

Rensselaer, NY · On-site

... and biotechnology contract research, development, and manufacturing, to identify top talent for ... Every other weekend required Position Overview The Quality Control Supervisor will oversee a team ...

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 ...

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 ...

TekWissen LLC

Quality Control Analyst

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 / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

Peregrine Team

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 ...

Pinnaql

Quality Control Manager

High Point, NC

... Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...

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

As of May 30, 2026, the average hourly pay for weekend biotech quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.
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Weekend Biotech Quality Control jobs near you

QC Specialist, Lab Services, II/III

Legend Biotech US

Raritan, NJ

Other

Posted yesterday

Job description

Legend Biotech is seeking QC Specialist, Lab Services, II/III as part of the Quality team based in Raritan, NJ. 

Role Overview

The QC Specialist, Lab Services is responsible for sample management. The QC Specialist is encouraged to work independently on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support to resolve some sophisticated issues. He/ She will serve as technical specialist within job function. Thinks logically and acts decisively.

Shift (Alternates Weekly) 

  • Wednesday-Saturday 5:00pm-4:00am 
  • Thursday-Saturday 4:00pm-4:00am

Key Responsibilities  

  • Prepares and reviews documentation independently.
  • Responsible for QC sample and retain management.
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems.
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and lab management software system (LIMS).
  • Prepare documents and coordinate Sample shipment (internal and external shipments).
  • Review logbooks and/ or LIMs to align physical quantities of samples in freezers/refrigerators.
  • Periodic inspection and consolidation of retains.
  • Document and perform sample management related non-conformance investigations.
  • Document and handle corrective and preventative action records.
  • Supports internal and regulatory audits.
Requirements
  • A minimum of a Bachelor's degree or higher.
  • A minimum of two (2) years related experience in medical device, biopharmaceutical, or pharmaceutical industry.
  • A degree in Biology, Biochemistry, Microbiology, Chemistry or related field.
  • Solid understanding of regulatory requirements, policies and guidelines.
  • Experience with Quality Control document reviews and regulatory inspection processes.
  • Working knowledge of Quality systems.
  • Experience in management of retain samples using electronic systems (eLIMS).
  • Candidates must be able to accommodate shift schedule. Shifts include weekend and evening work as required by the manufacturing process.
  • This position will be located in Raritan, NJ and may require up to 5% of travel.
  • This position will occasionally require to lift up to 20 pounds.

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