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Biotech Quality Control Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

QC Microbiologist

Raleigh, NC · On-site

$22 - $28.75/hr

Alliance Biotech Solutions is seeking a dedicated QC Microbiologist to support Environmental Monitoring (EM) and microbiological testing activities within a GMP manufacturing environment. This role ...

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 ...

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ . Shift: 3rd shift Wed-Sat Role Overview The Sr. QC Analyst is an exempt level position with ...

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Biotech Quality Control information

See salary details

$30.5K

$81.3K

$129.5K

How much do biotech quality control jobs pay per year?

As of Jul 9, 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.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

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.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

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 does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
More about Biotech Quality Control jobs
What cities are hiring for Biotech Quality Control jobs? Cities with the most 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 Biotech Quality Control jobs? States with the most job openings for Biotech Quality Control jobs include:
Infographic showing various Biotech Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 91% Full Time, 1% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Quality Control (QC) Analyst II

$24.75 - $33.25/hr

Other

Posted 3 days ago

New


Job description

Description

Position Summary


The Quality Control Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial biosimilar products in cGMP-compliant laboratories and will also be expected to be engaged in continuous improvement initiatives to drive efficiency and effectiveness of Kashiv's Quality Systems. 


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, 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.
  • Train other analysts to perform laboratory procedures and assays. Participate in internal assessments and audits as and when required.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

Minimum Qualifications:


Education:

  • Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 5 years of experience in a pharmaceutical/biotech QC laboratory. 
  • Alternatively, Master's degree in above areas with 3 years of experience in a pharmaceutical/biotech QC laboratory or PhD in above areas with a minimum of 2 years of experience. 

Preferred Qualifications: 


Experience:

  • Previous experience in a cGMP laboratory.
  • Strong background in protein chemistry and experience troubleshooting analytical results.
  • Demonstrated success at writing, revising, and complying with SOPs, protocols/reports, and QC methods.

Special Skills:

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

  • 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 requested.
  • Must be able to lift at least 25 lbs.
  • Ability to work under pressure and meet deadlines. 
  • High-paced environment structured to meet ambitious project goals
  • Some travel may be required

Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties, or skills 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.


Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.