Alnylam Pharmaceuticals
Engineer III Combination Product Quality Assurance
Alnylam Pharmaceuticals, Cambridge, Massachusetts, us, 02140
Engineer III Combination Product Quality Assurance
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Engineer III Combination Product Quality Assurance
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Alnylam Pharmaceuticals Engineer III Combination Product Quality Assurance
Join to apply for the
Engineer III Combination Product Quality Assurance
role at
Alnylam Pharmaceuticals Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Alnylam Pharmaceuticals Talent Acquisition- Biotechnology and Pharmaceutical
Overview The Engineer III - Combination Product Quality Assurance (CPQA) is responsible for providing quality oversight for the development and life cycle management for combination products at Alnylam. This role will work cooperatively with their counterparts throughout the combination product development team and QA providing quality oversight and support to ensure clinical through commercial lifecycle activities meet cGMP regulatory requirements and guidelines including Part 4 for combination products. This position reports to the Senior Manager of CPQA. This position is a hybrid role and is located at the Kendall Square location in Cambridge, Massachusetts. Key Responsibilities Review of post-market surveillance activities for an on-market program including device constituent and component QA support for change controls, complaints, and post-market surveillance meetings Provide new product and sustaining QA support for design and development activities of combination product design history, human factors, and risk management files. Provide quality support for notified body opinion submissions for significant changes Provide combination product QA support for Quality Management System (QMS) improvement efforts Collaborate with various CMOs and represent Alnylam QA. Help ensure that CMOs adhere to various requirements and oversee any required manufacturing changes. Identify and drive process/procedure improvements to increase efficiency. Lead and manage various QA feeder systems to ensure continued compliance. Qualifications Bachelor’s degree in engineering or sciences. Advanced degree preferred Minimum of 3 years of relevant experience, 5 years preferred, in a regulated industry preferably with medical device, combination product, or QA experience. Understanding of global Device and Combination Product regulations, standards, and guidelines (e.g., 21 CFR Part 4, Part 803, Part 820, ISO 13485, ISO 14971, ISO 62366) Ability to translate and implement evolving regulatory requirements into internal SOPs Proficient technical writing skills Excellent organizational, communication, and interpersonal skills including collaborating and working with a high functioning team About Alnylam : We are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values:
fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people . We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Quality Assurance Referrals increase your chances of interviewing at Alnylam Pharmaceuticals by 2x Sign in to set job alerts for “Product Quality Engineer” roles.
Hingham, MA $95,000.00-$125,000.00 2 weeks ago Cambridge, MA $97,440.00-$155,904.00 2 weeks ago Brockton, MA $70,000.00-$90,000.00 1 week ago Design Quality Engineer -Walpole, MA, 02032
Quincy, MA $72,800.00-$138,300.00 1 month ago Chelmsford, MA $75,000.00-$85,000.00 2 days ago Woburn, MA $81,226.00-$131,131.00 2 weeks ago Bedford, MA $110,000.00-$170,000.00 4 days ago Marlborough, MA $119,700.00-$199,400.00 2 weeks ago Quality Engineer (Second Shift) - Chelmsford, MA
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Join to apply for the
Engineer III Combination Product Quality Assurance
role at
Alnylam Pharmaceuticals Engineer III Combination Product Quality Assurance
Join to apply for the
Engineer III Combination Product Quality Assurance
role at
Alnylam Pharmaceuticals Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Alnylam Pharmaceuticals Talent Acquisition- Biotechnology and Pharmaceutical
Overview The Engineer III - Combination Product Quality Assurance (CPQA) is responsible for providing quality oversight for the development and life cycle management for combination products at Alnylam. This role will work cooperatively with their counterparts throughout the combination product development team and QA providing quality oversight and support to ensure clinical through commercial lifecycle activities meet cGMP regulatory requirements and guidelines including Part 4 for combination products. This position reports to the Senior Manager of CPQA. This position is a hybrid role and is located at the Kendall Square location in Cambridge, Massachusetts. Key Responsibilities Review of post-market surveillance activities for an on-market program including device constituent and component QA support for change controls, complaints, and post-market surveillance meetings Provide new product and sustaining QA support for design and development activities of combination product design history, human factors, and risk management files. Provide quality support for notified body opinion submissions for significant changes Provide combination product QA support for Quality Management System (QMS) improvement efforts Collaborate with various CMOs and represent Alnylam QA. Help ensure that CMOs adhere to various requirements and oversee any required manufacturing changes. Identify and drive process/procedure improvements to increase efficiency. Lead and manage various QA feeder systems to ensure continued compliance. Qualifications Bachelor’s degree in engineering or sciences. Advanced degree preferred Minimum of 3 years of relevant experience, 5 years preferred, in a regulated industry preferably with medical device, combination product, or QA experience. Understanding of global Device and Combination Product regulations, standards, and guidelines (e.g., 21 CFR Part 4, Part 803, Part 820, ISO 13485, ISO 14971, ISO 62366) Ability to translate and implement evolving regulatory requirements into internal SOPs Proficient technical writing skills Excellent organizational, communication, and interpersonal skills including collaborating and working with a high functioning team About Alnylam : We are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values:
fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people . We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another. At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer. Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Quality Assurance Referrals increase your chances of interviewing at Alnylam Pharmaceuticals by 2x Sign in to set job alerts for “Product Quality Engineer” roles.
Hingham, MA $95,000.00-$125,000.00 2 weeks ago Cambridge, MA $97,440.00-$155,904.00 2 weeks ago Brockton, MA $70,000.00-$90,000.00 1 week ago Design Quality Engineer -Walpole, MA, 02032
Quincy, MA $72,800.00-$138,300.00 1 month ago Chelmsford, MA $75,000.00-$85,000.00 2 days ago Woburn, MA $81,226.00-$131,131.00 2 weeks ago Bedford, MA $110,000.00-$170,000.00 4 days ago Marlborough, MA $119,700.00-$199,400.00 2 weeks ago Quality Engineer (Second Shift) - Chelmsford, MA
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr