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Quality Control Laboratory Manager Jobs in Boston, MA

Replimune

Scientist I, Quality Control

Framingham, MA · On-site

$112K - $146K/yr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Replimune-2

Scientist I, Quality Control

Framingham, MA · On-site

$112.50 - $146/hr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Replimune Group

Scientist I, Quality Control

Framingham, MA · On-site

$112.50 - $146/hr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.

Rentschler

Quality Control Data Reviewer

Milford, MA · Hybrid

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

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All JobsQuality Control Laboratory JobsQuality Control Laboratory Manager JobsQuality Control Laboratory Manager Jobs in Boston, MA

Quality Control Laboratory Manager information

See Boston, MA salary details

$33.1K

$88.3K

$140.7K

How much do quality control laboratory manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality control laboratory manager in Boston, MA is $88,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,700.00 and $108,600.00 per year, depending on experience, location, and employer.

What does a quality control laboratory manager do?

A Quality Control Laboratory Manager oversees the operations of a laboratory that tests products for quality and compliance with industry standards. They manage laboratory staff, ensure testing procedures are followed accurately, and maintain equipment. The manager is responsible for implementing quality assurance protocols, analyzing test results, and reporting findings to upper management. Their work helps ensure that products meet safety and quality requirements before reaching consumers.

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

To thrive as a Quality Control Laboratory Manager, you need a strong background in laboratory science, quality assurance, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and certifications such as ASQ Certified Quality Auditor are often required. Excellent leadership, problem-solving, and communication skills help manage teams and ensure smooth operations. These competencies are crucial for maintaining high standards, ensuring product safety, and meeting regulatory requirements in laboratory environments.

What are some common challenges faced by quality control laboratory managers, and how can they be addressed?

Quality Control Laboratory Managers often face challenges such as maintaining compliance with strict regulatory standards, managing a diverse team, and ensuring timely turnaround of test results. To address these, effective managers implement robust training programs, foster clear communication across teams, and establish standardized operating procedures. Proactive planning and continuous process improvement are key to staying ahead of regulatory updates and ensuring consistent data quality, which ultimately supports both operational efficiency and product safety.

What is the difference between Quality Control Laboratory Manager vs Quality Control Analyst?

AspectQuality Control Laboratory ManagerQuality Control Analyst
CredentialsBachelor's degree in science, often with management certificationsBachelor's degree in science or related field
Work EnvironmentSupervises lab staff, manages operations, oversees testing processesPerforms testing and analysis of samples under supervision
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for lab oversightCommonly employed in similar industries for sample analysis

The main difference is that the Quality Control Laboratory Manager oversees the entire lab operations and staff, ensuring compliance and quality standards, while the Quality Control Analyst focuses on conducting specific tests and analyses. The manager has more responsibilities related to supervision and process management, whereas the analyst is primarily involved in testing tasks.

What are the most commonly searched types of Quality Control Laboratory jobs in Boston, MA?

The most popular types of Quality Control Laboratory jobs in Boston, MA are:

What cities near Boston, MA are hiring for Quality Control Laboratory Manager jobs?

Cities near Boston, MA with the most Quality Control Laboratory Manager job openings:

Quality Control Laboratory Manager jobs near you
Infographic showing various Quality Control Laboratory Manager job openings in Boston, MA as of June 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $88,350 per year, or $42.5 per hour.

Scientist I, Quality Control

Framingham, MA • On-site

Replimune
Biotechnology Research and Development • 201 - 500 employees
Learn more about Replimuneexternal

$112K - $146K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 10 days ago

Job description

Overview
Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient's lives depend on it.
At Replimune, we live by our values:
United: We Collaborate for a Common Goal.
Audacious: We Are Bold.
Dedicated: We Give Our Full Commitment.
Candid: We Are Honest With Each Other.
People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.
Join us, as we reshape the future.
Job Summary:
The Scientist I/II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the responsibility of overseeing the work of junior QC staff and provide training for new analyst. The QC Analytical Scientist will be responsible for assisting with maintaining systems for QC Analytical Laboratory. The QC Analytical Scientist will be required to assist with scheduling, performing and reviewing of tests results of raw materials, in-process, drug substance and final drug product samples following established test method (SOPs). The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory.
This position is based in our Framingham location and typically has a 5-day on-site expectation.
Responsibilities
Key responsibilities:
The responsibilities of the QC Analytical Scientist include, but are not limited, to the following:
  • Establish, revise and maintain procedures for QC Analytical testing.
  • Maintain QC systems related to raw materials, in-process, drug substance and final drug product sample testing.
  • Review testing data of other analysts.
  • Assist with the maintenance of QC laboratory and equipment.
  • Responsible for the protocol and report generation of method qualifications related to QC tests.
  • Perform QC Analytical testing of raw materials, in-process, water and product samples following Standard Operating Procedures (SOPs).
  • Review and complete documentation in accordance with current Good Manufacturing Practices (cGMP).
  • Responsible for change control, deviations and CAPA's related to QC Analytical operations including conducting OOS, OOT, and lab investigations.
  • Assist with audits and regulatory inspections, as needed.
  • Assist with QC laboratory equipment validation.
  • Interact within internal, as well as across other functional groups to communicate QC Analytical requirements.
  • Oversee sampling and storage of QC samples and maintain regulatory/retention inventory.
  • Coordinate shipping of samples to contract testing laboratories.
  • Train of others within department within the scope of knowledge and responsibilities.
  • Understanding of USP/EP monograph testing/requirements.

Other responsibilities
  • Troubleshoot equipment and analytical test methods.
  • Manage technical studies performed with external companies with provision and review of reports.
  • Represent QC at inter-departmental meetings and interact with external vendors, as necessary.
  • Other tasks as assigned.

Qualifications
Education:
  • BA or BS in analytical chemistry or other related science, preferably with chemistry or coursework as part of the study program.

Required Experience:
  • 5+ years of experience working in GMP/GLP environment or similar set up.
  • Knowledge of Analytical techniques and technical experience, within a Analytical Lab is preferred.
  • Computer literacy (MS Word and Excel), good communication and organizational skills.
  • Ability to work well independently and with others in a team.
  • Good organizational skills

Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $112,500-$ $146,000. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate's unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.
At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.
About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune's proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.
We are an Equal Opportunity Employer.

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