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Remote Senior Quality Engineer Jobs in Massachusetts

Prenuvo

Senior QA Engineer

Boston, MA · Remote

We are looking for a Senior QA Engineer I to join our team! You will be responsible for ensuring ... This role is fully remote; however, we have a preference for candidates able to work in the Pacific ...

Actifio

Senior QA Enginerer

Waltham, MA · Remote

You will also work with cross-functional teams work with developers, Product Managers and Remote QA teams to develop software tests which verify and exercise product requirements. The candidate must ...

Motional

Senior Engineer

Boston, MA · On-site +1

$113K - $155K/yr

Ref. No. N270 BOSTON - REMOTE U.S. ONLY FULL-TIME What You'll Do: * Design, implement, and test ... Conduct code review and guide junior team members on code quality, correctness and efficiency.

Lantheus

Supplier Quality Senior Specialist

Bedford, MA · On-site +1

$86K - $119K/yr

Summary of role The Supplier Quality Senior Specialist is responsible for maintaining Lantheus ... The position can be either remote or hybrid, with occasional onsite requirements at the department ...

Symbotic

Senior Manufacturing Engineer

Boston, MA · Remote

$98K - $135K/yr

In close collaboration with Project Management, Quality Engineering, and external manufacturing ... bi-weekly. #LI-TS1 #LI-Remote About Symbotic Symbotic is an automation technology leader ...

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Remote Senior Quality Engineer information

What does a remote senior quality engineer do?

A Remote Senior Quality Engineer is responsible for ensuring the quality and reliability of software products by designing and implementing test strategies, identifying and troubleshooting defects, and collaborating closely with development teams. They often lead quality assurance (QA) initiatives, mentor junior engineers, and help define best practices for testing in a remote work environment. Their work includes both manual and automated testing, as well as creating and maintaining testing frameworks to ensure products meet high standards before release.

What are the key skills and qualifications needed to thrive as a remote senior quality engineer?

To thrive as a Remote Senior Quality Engineer, you need deep expertise in software quality assurance, test automation, and a strong understanding of programming concepts, commonly supported by a degree in computer science or related field. Familiarity with tools such as Selenium, Jenkins, Jira, and CI/CD systems, along with certifications like ISTQB, are typically required. Strong analytical thinking, self-motivation, and effective remote communication skills set outstanding candidates apart. These abilities ensure efficient collaboration, high product quality, and successful delivery within distributed engineering teams.

How does a remote senior quality engineer typically collaborate with cross-functional teams to ensure product quality?

As a Remote Senior Quality Engineer, you will regularly work with developers, product managers, and operations teams through virtual meetings, shared documentation, and collaboration tools. You are often responsible for leading test planning sessions, reviewing requirements, and providing feedback to ensure quality is considered early in the development cycle. Effective communication and proactive coordination are key, as you may need to bridge time zones and cultural differences to align quality standards. Utilizing project management and automation platforms is common to streamline workflows and maintain transparency across distributed teams.

What is the difference between Remote Senior Quality Engineer vs Remote Quality Analyst?

AspectRemote Senior Quality EngineerRemote Quality Analyst
CredentialsBachelor's in Engineering, Quality Management certifications (e.g., CQE)Bachelor's in related fields, QA certifications (e.g., ISTQB)
Work EnvironmentDesigning testing strategies, leading QA teams, collaborating with development teamsExecuting test cases, analyzing results, reporting defects
Industry UsageSoftware, manufacturing, tech companiesSoftware, IT services, product companies
Search/Comparison IntentUnderstanding senior QA roles, career progressionEntry to mid-level QA testing roles

The Remote Senior Quality Engineer typically leads testing efforts, designs quality strategies, and collaborates with development teams, requiring more experience and certifications. In contrast, a Remote Quality Analyst focuses on executing tests and reporting issues, often at an entry or mid-level. Both roles are vital in ensuring product quality but differ in responsibilities and seniority.

What are popular job titles related to Remote Senior Quality Engineer jobs in Massachusetts?

For Remote Senior Quality Engineer jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Remote Senior Quality Engineer jobs in Massachusetts look for?

The top searched job categories for Remote Senior Quality Engineer jobs in Massachusetts are:

What cities in Massachusetts are hiring for Remote Senior Quality Engineer jobs?

Cities in Massachusetts with the most Remote Senior Quality Engineer job openings:

Remote Senior Quality Engineer jobs near you
Infographic showing various Remote Senior Quality Engineer 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.

Remote Sr. Manager, GMP Quality

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

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

Job description

37609761 Remote Sr. Manager, GMP Quality, 6 Months Contract
Sigma Systems is currently looking for a Remote Sr. Manager, GMP Quality

Responsibilities:

  • Be the QA representative on cross-functional project teams. Responsible for communicating with the Quality and Production departments at domestic and international contract manufacturing organizations, and within SMPA's Quality, Supply Chain, CMC, and Commercial Manufacturing departments.
  • Conducts product release activities for clinical and commercial drug substances and drug products; including review and approval of Master Batch Records, Executed Batch Records, release and stability testing documentation, and batch disposition. These activities must be conducted in a timely manner to ensure continued product supply while ensuring Quality and Safety of the product.
  • Partners with CMC and Commercial Manufacturing to conduct technical transfers and validation of new or existing processes and products to domestic and international contract manufacturing organizations.
  • Supports commercial validation activities by reviewing validation protocols and reports.
  • Ensures compliance to existing procedures and supports continuous improvement opportunities by identifying areas where improvements and efficiencies can be gained through SOP and compliance standard revisions. Authors, reviews and approves standard procedures and electronic systems, as needed.
  • Leads, authors, reviews and/or approves CMOs Quality Events, Investigations, CAPA, Change Controls, and Complaints, as well as initiating in SMPA's eQMS, as needed. This may require timely interface with domestic and international suppliers.
  • Serves as Person-in-the-Plant, as needed.
  • Authors relevant sections of Annual Product Reviews by compiling appropriate data and metrics and making appropriate recommendations.
  • Other duties as assigned.

Requirements:

  • Minimum of Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or relevant field of study.
  • 8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role.
  • Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage formsand/or combination products.
  • Experience with managing external CMOs, contract laboratories, and third-party logistics suppliers.
  • Must have experience in reviewing and approving master and executed batch records and performing final disposition of drug substances and products.
  • Experience managing quality events (investigations, CAPA and change control), and working knowledge of formal risk management tools and assessments. The individual must demonstrate the ability to evaluate and assess technically complex quality events, as well as the ability to document these events with excellent technical writing skills.
  • Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows.
  • Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations.
  • Excellent verbal and written communication skills, including ability to interact effectively with senior management, partners, and project core team members.
  • Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of quality and compliance.