72 engine validation engineer opportunities in Cambridge updated today
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· Page 1 / 4*Company Description** Aumvis PharmaTec, established in 2008, is a premier provider of consulting, engineering, and technical solutions to Pharma, Bio-Pharma, Biotech, Medical Device, and related industries. With offices in the United States and Canada, the company specializes in delivering quality
Company Description Aumvis PharmaTec, established in 2008, is a premier provider of consulting, engineering, and technical solutions to Pharma, Bio-Pharma, Biotech, Medical Device, and related industries. With offices in the United States and Canada, the company specializes in delivering quality and
*Responsibilities:** Perform start-up, commissioning, qualification, validation and revalidation for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, medical device, and drug product manufacturing processes. *Strategic Focus Area:** Develops into a subject
*Summary of Primary Responsibilities:** This position is responsible for leading and performing the Bedford Site’s Validation projects that includes start-up, commissioning, qualification, validation and revalidation for facility, equipment, critical utility, automation/computer system, cleaning, st
Please candidates make sure you are speaking to them about the IVD / IVDR requirements, and this should be clearly on your resume. Please send with 2 references as well. Title: Validation Engineer Duration: 1 year + Location: Massachusetts & NH - 100% onsite Job Description: We are seeking a sea
*Computer Systems Validation Engineer** *Location: Norwood, MA** *Duration: 12 Months** *USC, GC, GC-EAD and H4-EAD** *Rate: $65-70/hr. on C2C** *open to relocation candidates but MUST relo from day 1\*\*** *Job Description:** GxP Systems Engineer who will serve a key role supporting the Validation,
*Title: Software Quality & Validation Consultant** *Location: Andover, MA (Local Only)** *Duration: 12+ Months ContractUSC, GC, GC EAD, H4 EAD, TN** *Interview - 2 rounds. First round is virtual and 2** *nd** *round is probably onsite** *Job Description** Strong with quality software validations
*Job Summary:** The Principal Commissioning & Validation Engineer will lead validation activities to ensure GMP compliance across manufacturing, laboratory equipment, and computerized systems. This role supports QMS processes, validation documentation, and cross-functional collaboration to maint
Role: Computer Systems Validation Engineer Location: Norwood, MA GxP Systems Engineer who will serve a key role supporting the Validation, Delivery and Administration of the GxP laboratory benchtop computerized systems and Enterprise systems. This role will be a member of the Digital Quality team an
Date Posted: 2026-03-30 Country: United States of America Location: US-MA-ANDOVER-AN3 ~ 354 Lowell St ~ AN3 SUFFOLK BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to st
*Description** *Verista's** 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies s
*Date Posted:** 2026-01-29 *Country:** United States of America *Location:** US-MA-ANDOVER-AN2 ~ 352 Lowell St ~ AN2 HAMPSHIRE BLDG *Position Role Type:** Onsite *U.S. Citizen, U.S. Person, or Immigration Status Requirements:** The ability to obtain and maintain a U.S. government issued security cle
About Marvell Marvell's semiconductor solutions are the essential building blocks of the data infrastructure that connects our world. Across enterprise, cloud and AI, and carrier architectures, our innovative technology is enabling new possibilities. At Marvell, you can affect the arc of individual
*Job Description** Strong with quality software validations Strong/recent Med device industry experience is preferred, if not then pharma or biotech works. Any is required Will be supporting ongoing projects from the quality validation size initiatives Needs someone that can work cross functionally
Title: Validation Engineer Location: Massachusetts – 100% Onsite Job Description: We are looking for an experienced Validation Engineer with over 10 years of expertise in medical device or other regulated manufacturing environments. The ideal candidate will have strong hands-on experience in develop
*TITLE: Validation Engineer (Consultant)** *Location: Boston, MA** *Duration: 06+ Month contract** POSITION SUMMARY The Validation Engineer will report to the VCGT Validation leadership or an appropriate designee to execute Commissioning, Qualification and Validation activities for Cell and Gene The
Country: United States of America Location: US-NH-PELHAM-PE2 ~ 50 Bush Hill Rd ~ BLDG 2 Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: Active and transferable U.S. government issued security clearance is required prior to start date. U.S. citizenship is req
About Marvell Marvell’s semiconductor solutions are the essential building blocks of the data infrastructure that connects our world. Across enterprise, cloud and AI, and carrier architectures, our innovative technology is enabling new possibilities. At Marvell, you can affect the arc of individual
*Why Patients Need You** Our breakthroughs would not make it to the hands of patients without our validation team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their wo
*Date Posted:** 2026-03-25 *Country:** United States of America *Location:** US-NH-PELHAM-PE2 ~ 50 Bush Hill Rd ~ BLDG 2 *Position Role Type:** Onsite *U.S. Citizen, U.S. Person, or Immigration Status Requirements:** Active and transferable U.S. government issued security clearance is required prior
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to mo
*COMPANY DESCRIPTION:** A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to
Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Women's Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary focus on innovation in Women's Health, premised on our
Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Women’s Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary focus on innovation in Women’s Health, premised on our
In this highly visible role, you will perform lab characterization and validation of various analog & mixed signal embedded circuits; and collaborate with multi-functional teams to launch the world's most premiere mobile SoC’s. At Apple, we work every single day to craft products that enrich peo
Compensation will be determined based on the candidate’s level of experience and qualifications Be part of a mission that matters—join Theragenics as a Validation & Verification Engineer and help ensure the safety, quality, and performance of life-saving medical devices used in cutting-edge cancer t
Sequel Med Tech*About Sequel** Sequel, headquartered in Manchester, New Hampshire, is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. Sequel’s approach is to look at diabetes management holistically to advance systems that make living with diabetes simp
Coordinates testing activities to ensure equipment, machinery and systems are performing as expected. Designs and develops validation studies and test cases. Writes and reviews validation documentation as it relates to mechanics, computers and other equipment. 5-10 Years Experience. See attached Job
Job Description: The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols, test plans, various validation
$83,000 – $130,000/year
Estimation confidence: Low
Estimate based on market data for Cambridge. Actual salaries may vary depending on experience, company, and area.
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