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Weekend Biotech Quality Control Jobs (NOW HIRING)

Kashiv BioSciences, LLC

QC Analyst II

Piscataway, NJ

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 ... Must be able to work extended hours or weekend hours, as may be required. Noise: No extraordinary ...

Kashiv BioSciences, LLC

QC Analyst III

Piscataway, NJ

$24 - $32.25/hr

Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 ... Must be able to work extended hours or weekend hours, as may be required. Noise: No extraordinary ...

Kashiv Biosciences LLC

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

... in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of ... hours or weekend hours, as may be required. Noise: • No extraordinary noise levels. Standing ...

Kashiv Biosciences LLC

QC Analyst II

Piscataway, NJ · On-site

$24 - $32.25/hr

... biotech QC laboratory. Experience: • Previous experience in a cGMP laboratory. • Strong ... hours or weekend hours, as may be required. Noise: • No extraordinary noise levels. Standing ...

Legend Biotech

Sr. QC Analyst

Raritan, NJ

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Shifts include routine weekend and evening work as required by the manufacturing process.

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Shifts include routine weekend and evening work as required by the manufacturing process.

Legend Biotech US

QC Analyst II

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Shifts include routine weekend and evening work as required by the manufacturing process.

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Shifts include routine weekend and evening work as required by the manufacturing process.Candidates ...

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Shifts include routine weekend and evening work as required by the manufacturing process.Candidates ...

Actalent

QC Sample Coordinator

Raleigh, NC

$19.25 - $26.50/hr

At least 2 years of experience in GMP pharmaceutical, medical device, or biotech QC/QA operations ... off-shift or weekend coverage as needed to support sample receipt, testing schedules, and ...

Actalent

QC Sample Coordinator

Raleigh, NC

$19.25 - $26.50/hr

At least 2 years of experience in GMP pharmaceutical, medical device, or biotech QC/QA operations ... off-shift or weekend coverage as needed to support sample receipt, testing schedules, and ...

BioPhase Solutions

QC Inspector

San Diego, CA

$18 - $19.80/hr

... biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join ... weekends as needed Key Responsibilities: * Perform routine and special inspections for visual ...

Cellectis

Director, Quality Control

Raleigh, NC

Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles. * Strong leadership skills with experience building and leading high-performing technical ...

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

As of May 29, 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 Analyst II

Kashiv BioSciences, LLC

Piscataway, NJ

$24 - $32.25/hr

Other

Posted 24 days ago

Job description

Description

 Position Summary


The QC Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required.


Essential Duties & Responsibilities


  • Analytical testing to support product in-process, release, Raw materials and stability programs.
  • Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.
  • Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.
  • Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards
  • Perform the investigation analysis during the non-conformance.
  • Conduct the investigation process as a part of Quality Event and work with supervisor to close the investigation.

Requirements

 Position Requirements and Qualifications


Education:


Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in above areas with 6 years of experience in a pharmaceutical/biotech QC laboratory.


Experience:  


Previous experience in a cGMP laboratory.

Strong background in small molecule and protein chemistry and experience troubleshooting analytical results.

Demonstrated success at writing, revising, and complying with SOPs, policies, and QC methods.


Specialized Knowledge and Skills: 


Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. 

Knowledge of and experience with Empower and/or Shimadzu software

Previous experience supporting regulatory inspections (e.g. PAI).

Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies.


Work Environment & Physical Demands:


General Working Environment:


Some time spent in an office doing office work (reading, writing, reviewing, and editing documents).

Significant amount of time spent in the laboratory.

Must be able to work extended hours or weekend hours, as may be required.

Noise:

No extraordinary noise levels.

Standing/Lifting:

Must be able to lift at least 25 lbs.

Visual:

No extraordinary requirements.

Stress:

High-paced demanding environment to meet ambitious project goals.

Travel:

No travel required.


Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

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