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Quality Operations Manager Jobs in Massachusetts

Operations Manager

Pembroke, MA · On-site

$57K - $65K/yr

Facility Management Corporation, known as "FMC Ice Sports," was formed in 1992 to deliver high ... We have established a record of quality operations and have grown to be the largest operator of ...

Operations Manager

Marlborough, MA · On-site

$57K - $65K/yr

We have established a record of quality operations and have grown to be the largest operator of ... The Operations Manager , reporting directly to the Arena Manager, will oversee operations including ...

Operations Manager

West Roxbury, MA · On-site

$57K - $65K/yr

We have established a record of quality operations and have grown to be the largest operator of ... The Operations Manager , reporting directly to the Arena Manager, will oversee operations including ...

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Quality Operations Manager information

See Massachusetts salary details

$42K

$99.4K

$151.3K

How much do quality operations manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for quality operations manager in Massachusetts is $99,435.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $120,100.00 per year, depending on experience, location, and employer.

How does a quality operations manager typically collaborate with other departments to maintain product standards?

A Quality Operations Manager works closely with departments such as production, supply chain, and R&D to ensure that product quality standards are consistently met. They often participate in cross-functional meetings to address quality concerns, analyze root causes of issues, and implement corrective actions. Effective communication and teamwork are essential, as the manager needs to align quality objectives with overall business goals and foster a culture of continuous improvement across teams.

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

To thrive as a Quality Operations Manager, you need expertise in quality management systems, process improvement, and a background in engineering or a related field, often supported by a bachelor’s degree. Familiarity with ISO standards, Six Sigma or Lean methodologies, and quality management software is typically required. Strong leadership, problem-solving abilities, and effective communication skills help drive quality initiatives and foster a culture of continuous improvement. These competencies are crucial to ensuring product consistency, regulatory compliance, and operational excellence.

What is the role of a quality operations manager?

A quality operations manager oversees the implementation and maintenance of quality systems to ensure products and services meet company standards and regulatory requirements. They analyze processes, lead quality improvement initiatives, and often use tools like Six Sigma or ISO standards to enhance efficiency and compliance.
What are popular job titles related to Quality Operations Manager jobs in Massachusetts? For Quality Operations Manager jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Quality Operations Manager jobs in Massachusetts look for? The top searched job categories for Quality Operations Manager jobs in Massachusetts are:
What cities in Massachusetts are hiring for Quality Operations Manager jobs? Cities in Massachusetts with the most Quality Operations Manager job openings:
Infographic showing various Quality Operations Manager job openings in Massachusetts as of June 2026, with employment types broken down into 80% Full Time, 18% Part Time, 1% Temporary, and 1% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $99,435 per year, or $47.8 per hour.

Manager, Quality Operations

Amylyx Pharmaceuticals

Cambridge, MA • On-site

Full-time

Posted 23 days ago


Job description

The Opportunity

This position is responsible for providing CMC quality oversight of sterile drug product and finished drug product manufacturing, labeling, packaging and distribution operations.

As the GMP quality expert, this role is accountable for ensuring all company, regional, and global GMP and GDP standards and regulations are met, and that the GMP Quality department performs to a standard that ensures the quality of products and materials produced by Amylyx contracted partners. 

We anticipate hiring the Manager, Quality Operations in September 2026. 

Responsibilities

  • Provide quality oversight of Drug Product and Finished Drug Product production activities.
    • Provide QA review and approval on sterile drug product process validation documents, equipment validation documents, master production records, product specifications (in-process, release, and stability), analytical method qualification/validation documents, method transfer documents, and stability plans.
    • Review executed Batch Production and QC Control Records to ensure all approved procedures were followed and all specifications are met.
    • Prepare and /or approve batch disposition packages.
    • Provide QA review and approval on quality system records, including but not limited to deviations, OOS, change controls, CAPAs, and product quality complaints.
    • Lead or participate in regular meetings internally and externally as Quality SME to ensure Amylyx's quality expectations are met in the areas of Good Manufacturing Practice, Good Distribution Practice, and Good Documentation Practice.
  • Write, review and/or approve SOPs as QA SME for manufacturing, labeling, packaging, and transportation of late stage and commercial products.
  • Provide QA review on NDAs. Assure that source data and information used in regulatory submissions and validation activities is maintained and traceable.
  • Support FDA, EMA or other regulatory agency inspections.

Required Qualifications

  • Bachelor's degree with 5+ years of experience in Quality Operations, Quality Control (QC), Manufacturing Science & Technology (MSAT), or related pharmaceutical manufacturing functions; or Advanced degree (Master's, PhD, or equivalent) with 3+ years of experience in Quality Operations, Quality Control (QC), Manufacturing Science & Technology (MSAT), or related pharmaceutical manufacturing functions.
  • Must have at least 3 years of hands-on experience supporting sterile or aseptic manufacturing environments, including but not limited to quality operations, QC, MSAT, etc.
  • Experience with authoring and reviewing NDA CMC sections and addressing Regulatory Filing requirements in FDA cGMP regulations, Eudralex and ICH Guidance, as well as other Biopharma industry guidance and regulations.
  • Ability to work with all levels of the organization and external contract service providers to ensure compliance with current regulations.
  • Travel may be required up to 10% within US, which may include on-site review of third-party operations.

Preferred Requirements

  • Experience with environmental monitoring is highly preferred.
  • Direct experience with serialization is highly preferred.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.