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Manager Biotech Quality Control Jobs in Massachusetts

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

Role Description As a Quality Control Manager at Borg Design Inc., you will be responsible for overseeing the quality of all machined parts produced by our team. This role is based in Hudson, MA and ...

... biotech. Responsibilities * Manage phase appropriate stability, specification and reference ... Serve as QC point of contact for CDMOs/CTLs ensuring appropriate quality control oversight of ...

Quality Control Manager

Pittsfield, MA · On-site

$80K - $110K/yr

Quality Control Manager Job Overview Pay : $80,000- $110,000 We are seeking an experienced Quality Control Manager to lead and manage all quality operations throughout the manufacturing process. This ...

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Manager Biotech Quality Control information

What does a manager biotech quality control do?

A Manager Biotech Quality Control oversees the quality assurance processes within a biotechnology company, ensuring that products meet regulatory standards and internal specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products, and analyze data to identify trends or issues. This role also involves setting quality control policies, training staff, and liaising with regulatory bodies to maintain compliance. Managers in this field play a crucial role in product safety and efficacy, directly impacting the success of biotech products in the market.

What are the key skills and qualifications needed to thrive as a manager biotech quality control?

To thrive as a Manager Biotech Quality Control, you need a strong background in biology or chemistry, extensive knowledge of quality assurance regulations, and typically a bachelor’s or master’s degree in a life science field. Familiarity with laboratory information management systems (LIMS), GMP (Good Manufacturing Practices), and certifications such as ASQ or Six Sigma are highly valued. Leadership, attention to detail, and strong problem-solving and communication skills help you guide teams and ensure compliance. These skills and qualities are critical for maintaining product quality, regulatory adherence, and the overall success of biotech manufacturing operations.

What are the most common challenges faced by a manager biotech quality control, and how are they typically addressed?

Managers in Biotech Quality Control often face challenges such as ensuring regulatory compliance, maintaining rigorous documentation, and managing a team with diverse expertise. Keeping up-to-date with changing industry standards and regulatory requirements is crucial, as is fostering a culture of continuous improvement and clear communication. These challenges are typically addressed through ongoing staff training, implementing robust quality management systems, and close collaboration with other departments like R&D and manufacturing to ensure that quality standards are consistently met.

What is the difference between Manager Biotech Quality Control vs Quality Control Specialist?

AspectManager Biotech Quality ControlQuality Control Specialist
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's in Life Sciences or related field, Quality Certifications preferred
Work EnvironmentOversees QC teams, manages testing processes, and ensures compliancePerforms testing, data analysis, and reports results
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech, pharma, and manufacturing sectors

The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.

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 Manager Biotech Quality Control jobs in Massachusetts?

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

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

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

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

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

Infographic showing various Manager Biotech Quality Control job openings in Massachusetts as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 3% Contract, and 3% Nights. Highlights an 100% In-person job distribution.

Pharmaceutical Quality Control Associate

Randstad

Norwood, MA

$41 - $42/hr

Full-time

Posted 3 days ago

New


Job description

Ready to Make an Impact in Biotech Quality Control?

Join a high-performing team dedicated to advancing life-saving therapies! We are seeking a detail-oriented Quality Control Associate II to support cGMP QC testing for raw materials, drug substances, and finished products at our state-of-the-art manufacturing facility.

In this hands-on, on-site role, you will execute and troubleshoot core analytical methods, drive method transfers, and ensure absolute compliance with cGMP standards. If you excel in a fast-paced environment and want to apply your testing expertise directly to patient safety, this opportunity is for you!

The Role The Quality Control Associate II will support cGMP QC testing for raw materials, drug substances, and finished products at the company's manufacturing facility and affiliated contract organizations. This role includes executing and troubleshooting analytical methods, supporting method transfers, qualification activities, and ensuring compliance with cGMP standards. This is an on-site position.Here’s What You’ll Need (Basic Qualifications) Education: BA/BS DegreeExperience: STEM degree with 3-5 years’ of experience in a cGMP laboratory setting, with hands-on experience in mammalian cell culture, cell based and potency assays, ELISA, molecular biology, and Protein Analysis.Here’s What You’ll Bring to the Table (Preferred Qualifications)
  • Method development/qualification experience with molecular biology, cell-based assays, or protein analysis methods.
  • Trained in Aseptic techniques and general laboratory instrumentation (e.g. pH meters, balances, pipettes)
  • Ability to prepare reagents, pipette small volumes, work in a Biological Safety Cabinet
  • Experience with laboratory equipment calibration and maintenance.
  • Ability to work effectively in a fast-paced, cross-functional matrix environment.
  • Familiarity with relevant FDA, EU, ICH guidelines, and regulations.
INTERESTED? APPLY NOW! THESE POSITIONS FILL FAST! salary: $41 - $42 per hour
shift: First
work hours: 8 AM - 5 PM
education: Bachelors

Responsibilities

  • Execute QC molecular biology and Bioassay methods (e.g. Mammalian cell based potency, qPCR, sequencing, protein analysis)
  • Assist in troubleshooting equipment and assay issues.
  • Perform general laboratory support activities including reagent preparation, equipment maintenance, housekeeping, logbook reviews, etc.
  • Establish and maintain a safe laboratory working environment.
  • Write, revise, and maintain SOPs, protocols, and reports.
  • Support training as assigned.
  • Assist in execution of Quality records (i.e. investigations, change controls, CAPAs)
  • Ensure compliance with cGMP documentation and regulatory guidelines.
  • Accountable for all mandatory training and assigned tasks.
  • Provide support during audits and collaborate on continuous improvement initiatives.
  • Additional duties may be assigned.

Skills
  • Quality Control
  • Quality Assurance
  • cGMP
  • GMP
  • raw materials
  • Drug Substance
  • ELISA (1 year of experience is required)
  • mammalian cell culture
  • cell based and potency assays
  • molecular biology

  • Qualifications
  • Years of experience: 2 years
  • Experience level: Experienced

  • Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


    Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
    This posting is open for thirty (30) days.
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.


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About Randstad USA

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Our business is supporting business productivity, from matching the right people with great jobs to custom project solutions and consulting. We use innovative technologies and a passion for people to provide you with the best experience possible. We provide outsourcing, staffing, consulting and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. We can’t wait to tell you all about it.

Industry

Recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Minneapolis, MN, US