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Quality Control Laboratory Manager Jobs in Rutland, MA

Scientist I, Quality Control

Framingham, MA ยท 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 ...

Quality Control Data Reviewer

Milford, MA ยท 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 ...

Quality Control Data Reviewer

Milford, MA ยท 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 ...

QC Analyst

Devens, MA

$26.75 - $36/hr

Quality Control Analyst Location: Devens, MA Duration: 6 Months(extension up to 3 year) QC ... Work in a cGMP laboratory and manufacturing environment following techniques which require one to ...

Quality Control Data Reviewer

Milford, MA ยท 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 ...

Sr. QC Analyst, Microbiology

Hopkinton, MA

$26.25 - $35.50/hr

... Management. * Ability to prepare technical data and present to senior leadership. WHAT YOU WILL ... Experience in a cGMP QC laboratory environment performing environmental monitoring, contamination ...

New

Manager, Quality Control Lab

Devens, MA ยท On-site

$122K - $168K/yr

You will manage the laboratory's physical and human resources to ensure the facility is fully equipped to support aggressive production ramps. Your goal is to standardize and scale QC operations ...

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 ...

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 ...

Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives, and microbiological program execution. * Develop and deliver aseptic technique and contamination ...

New

Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives, and microbiological program execution. * Develop and deliver aseptic technique and contamination ...

New

QC Microbiologist II

Hopkinton, MA ยท On-site

$74K - $85K/yr

... * Assist QC management to author, review and approve documentation. * Assist QC management to ... General laboratory housekeeping Qualifications * Bachelor's degree in a relevant field and a ...

... * Assist QC management to author, review and approve documentation. * Assist QC management to ... General laboratory housekeeping Qualifications * Bachelor's degree in a relevant field and a ...

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Quality Control Laboratory Manager information

See Rutland, MA salary details

$32.2K

$85.8K

$136.7K

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

As of Aug 7, 2026, the average yearly pay for quality control laboratory manager in Rutland, MA is $85,832.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,900.00 and $105,500.00 per year, depending on experience, location, and employer.

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 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 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 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 cities near Rutland, MA are hiring for Quality Control Laboratory Manager jobs? Cities near Rutland, MA with the most Quality Control Laboratory Manager job openings:

Scientist I, Quality Control

Replimune

Framingham, MA โ€ข On-site

$112K - $146K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 18 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.