14 validation opportunities in Bedford updated today
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What You’ll Do The Validation Engineer II performs start-up, commissioning, qualification, validation, and revalidation activities for facility, equipment, critical utilities, automation/computer systems, cleaning, sterilization, medical device, and drug product manufacturing processes. This role de
Job Title: Sr. Validation Engineer Summary: This position supports the parenteral pharmaceutical manufacturing facility through the qualification and/or validation of equipment, raw materials, and manufacturing processes. Validation activities include research, protocol writing/execution and final r
PCI Pharma ServicesLife changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the futu
PCI Pharma ServicesA leading pharmaceutical services provider seeks a Validation Director to lead validation operations across PCI's sites. The role demands 15+ years of experience in pharmaceutical validation, strong leadership skills, and a solid understanding of regulatory requirements. Candidates should have a str
PCI Pharma ServicesLife changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the futu
A healthcare technology company in Bedford, MA is seeking a Senior Process Engineer to lead diverse process improvement initiatives in medical device manufacturing. The role involves designing and validating equipment, optimizing processes using methodologies like Six Sigma and Lean, and collaborati
Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix h
Merck KgaAWork Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcar
EMD Millipore CorporationWork Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcar
Anika TherapeuticsResponsibilities: 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 matter
Anika TherapeuticsSummary 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, steri
Position Summary Odyssey Systems has an exciting opportunity for a Senior Test Manager within our AFLCMC/HBG group. The C2ISR Division is responsible for a diverse portfolio that provides "cradle-to grave" support for the U-2 aircraft, E-8C Joint Surveillance Target Attack Radar System (JSTARS) airc
PhilipsJob Title Design Quality Engineer Job Description The Design Quality Engineer is responsible for the entire design control process, from validating design inputs to overseeing verification, validation, and design transfer, as well as leading comprehensive process validation strategies to ensure new
Ultragenyx PharmaceuticalWhy Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, th
Title : Manufacturing Validation Engineer Openings: 1 Duration: 12‑month contract (rolling), expected 4-5yr min total duration Hourly Pay : Starting at $50/hr Location: Raynham, MA 02767 5 days per week onsite Target Start : 6/1 Interview Process : 2 rounds Must‑Haves Bachelor of Science in Manufact
NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title : Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Locat
Position Summary The Validation Manager is responsible for leading validation strategy, execution, and lifecycle management for pharmaceutical or biotech manufacturing systems, with a strong focus on sterile processes. This role requires hands-on expertise in protocol authorship (IQ/OQ/PQ), project
Overview The Intern will assist validation department with routine validation tasks to include: Temperature Controlled Unit Mapping utilizing a validator and other data capture equipment, General report writing and generation of system database and list for qualified systems. Temperature mapping is
Summary: Supports testing and validation activities for medical devices, ensuring compliance with regulatory and quality standards. bility to interpret engineering drawings and specifications. Roles & Responsibilities: Develop Test Protocols aligned with design verification plans and regulatory
Drunix Solution IncJob Title: Project Lead - Validation (Supervisor) Full-Time Work Location: Fall River, MA Work Hours: General Shift: 8:30AM – 5:00PM (May very based on business needs) Duties and Responsibilities: • Design, review and approve protocols for equipment and processes to produce pharmaceutical drug produ
This role is responsible for supporting base business operations and smaller-scale projects while driving process changes and continuous improvement initiatives. The position focuses on reducing scrap, optimizing manufacturing efficiency, and managing non-conformance investigations by implementing e
Validation Engineer Apex Systems is hiring for a Validation Engineer to work for one of our top Medical Device clients. Job: Validation Engineer Type: 18 month contract Location: Raynham, MA Requirements/Responsibilities: Minimum of B.S. In Engineering 3 + yrs. of experience in Med Device (Ortho pre
CAIAre You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled per
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Bedford. Actual salaries may vary depending on experience, company, and area.
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