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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 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in ...

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 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, master's degree in ...

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 ... QC laboratory. Alternatively, master's degree in above areas with 8 years of experience in a ...

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

Thermo Fisher Scientific

Team Leader, QC

Fair Lawn, NJ · On-site

Chemistry, Biology, Biotechnology, Pharmaceutical Sciences, or related scientific field • ... QC activities with manufacturing timelines • Strong focus on safety leadership, including ...

Legend Biotech

Sr. QC Analyst

Raritan, NJ

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role Overview The Sr. QC Analyst is an exempt level position with responsibilities for performing Q ...

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, including hands-on experience with sample management, LIMS, or stability and environmental ...

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, including hands-on experience with sample management, LIMS, or stability and environmental ...

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 ...

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

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

Cellectis

Director, Quality Control

Raleigh, NC · On-site

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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Biotech Quality Control information

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$30.5K

$81.3K

$129.5K

How much do biotech quality control jobs pay per year?

As of May 29, 2026, the average yearly pay for biotech quality control in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.
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What cities are hiring for Biotech Quality Control jobs? Cities with the most Biotech Quality Control job openings:
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Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in the United States as of May 2026, with employment types broken down into 8% As Needed, 8% Full Time, and 84% Part Time. Highlights an 6% Physical, and 94% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

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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