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Biotech Quality Control Jobs in Massachusetts (NOW HIRING)

QC Analyst 1

Watertown, MA · On-site

$26 - $35/hr

The Quality Control - Analytics department supports a growing portfolio of cell and gene therapy ... biotechnology manufacturing environment, ideally with hands-on experience in cell and/or gene ...

Quality Control Analyst II Discover Veranova: At Veranova, we believe people are our most important ... and biotech customers. With deep technical expertise and impressive flexibility, we develop ...

Showing results 21-40

Biotech Quality Control information

See Massachusetts salary details

$33.3K

$88.8K

$141.4K

How much do biotech quality control jobs pay per year?

As of Sep 5, 2026, the average yearly pay for biotech quality control in Massachusetts is $88,815.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,100.00 and $109,200.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

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 does a biotech quality control do?

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.

What are the key skills and qualifications needed to thrive in biotech quality control?

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 most commonly searched types of Biotech Quality Control jobs in Massachusetts?

The most popular types of Biotech Quality Control jobs in Massachusetts are:

What are popular job titles related to Biotech Quality Control jobs in Massachusetts?

For Biotech Quality Control jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Massachusetts look for?

The top searched job categories for Biotech Quality Control jobs in Massachusetts are:

What cities in Massachusetts are hiring for Biotech Quality Control jobs?

Cities in Massachusetts with the most Biotech Quality Control job openings:

Infographic showing various Biotech Quality Control job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $88,815 per year, or $42.7 per hour.

Quality Control Analyst II

Celldex Therapeutics

Fall River, MA • On-site

$76K - $99K/yr

Full-time

Medical, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.


Job description

Individual is responsible for performing and understanding all tasks associated with the performance of routine laboratory work. Duties include performing QC testing, trending data and creating/revising SOPS. Assignments are provided by department management and are completed with minimal supervision.


  • Support environmental monitoring of air, equipment and surfaces in ISO Class 5, 7 and 8 clea rooms, including in-process and personnel monitoring.
  • Support sampling of USP Purified Water system aseptically.
    Support microbial bioburden and TOC testing on USP/EP Purified Water/equipment cleaning samples.
  • Participate in the enumeration and identification of microorganisms isolated in the facility.
  • Perform in-process, release, stability, and raw material testing on product and materials according to Product Specifications, SOPs, stability protocols and USP/EP.
  • Support growth promotion of media used in production and product testing.
  • Participate in Laboratory and Out of Specification Investigations.
  • Assist in training of new employees.
  • Database entry for trending programs and data filing.
  • Create and revise SOPs and reports.
  • Participate in compendial method verifications for raw materials and Celldex products.
  • Perform inventory and order chemicals and general lab supplies.
  • Perform routine preventive maintenance and equipment troubleshooting.
  • Coordinate and assist with onsite vendor activities for annual maintenance and equipment repairs.
  • Support method transfer from Analytical Development to Quality Control.
  • Support critical reagent inventory and requalification program.
  • Participate in shipment of Celldex products for external testing.
  • Perform other additional job-related duties as required.

  • Bachelor’s degree in Biology, Chemistry or related discipline.
  • Minimum of 2 years of experience in Biotech/Pharma industry.
  • Familiar with standard concepts, practices, and procedures within a quality control organization.
  • Experience with various laboratory instrumentation, software, and analytical methods.
  • Experience with cGMP and aseptic technique preferred.
  • Must have good understanding of Microsoft Windows Software Packages.
  • Adaptable to last-minute changes.

  • Strong communication and organizational skills.

  • Working knowledge of raw material testing, microbiological assays, capillary electrophoresis, ELISA, cell-based assays and/or HPLC testing.

  • The ability to work independently and as part of a team.

  • Flexibility in schedule for performing testing during weekdays, weekends, and holidays.


The expected base salary for this position is: $76374.00 to $99188.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Subject to eligibility and applicable plan terms, compensation includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.