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Computerized System Validation Jobs In Stow, Massachusetts - 29 Job Positions Available

1 – 20 of 29 jobs
Alkermes jobs

This position provides leadership and accountability for Digital Quality across the organization’s Quality, Regulatory, and R&D systems landscape, with responsibility for supporting computer system validation activities in alignment with applicable regulatory expectations, internal procedures, and data integrity requirements. The

Alkermes  10 days ago
Bristol Myers Squibb jobs

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

Bristol Myers Squibb  3 days ago
Sanofi jobs

Job Title: Location: Framingham, MA About The Job: The Automation and Manufacturing Systems (AMS) group is at the forefront of Sanofis digital transformation journey, driving operational excellence through innovative technology solutions and smart manufacturing initiatives. As a

Sanofi  15 days ago
Verista jobs

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

Verista  14 days ago
Bristol Myers Squibb jobs

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

Bristol Myers Squibb  7 days ago
Stantec jobs

Commissioning/Validation Specialist Stantecs Buildings team is on a mission to become the worlds leading integrated design practice. Our architects, engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design. Our collaborative culture

Stantec  1 day ago
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BioTalent jobs

An innovative, clinical-stage biotechnology company focused on developing transformative therapies for patients with serious genetic diseases is seeking a Senior IT Business Analyst to support its regulated GxP systems landscape. This individual will partner closely with Quality

BioTalent  12 hours ago
Ardelyx jobs

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients. Team

Ardelyx  5 days ago
JLL jobs

This job is with JLL, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. JLL empowers you to shape a

JLL  15 days ago
Confidential jobs

Executive Director, QMS & Digital About the Company Innovative pharmaceutical company specializing in oral therapeutics for metabolic & mineral disorders Industry Pharmaceuticals Type Public Company Founded 2007 Employees 201-500 Categories Pharmaceuticals Biotechnology Health Care Medical Conditions

Confidential  1 day ago

QC Data Integrity Program Manager Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially

Rentschler Biopharma  4 days ago
Maverick Technology Partners jobs

Looking for a Project Manager / Business Analyst for a 6-month contract 5 days on-site in Lexington, MA Local candidates only Must Haves: 5-7+ years of experience in a business analyst, project manager, or hybrid IT

Maverick Technology Partners  1 day ago

Job Title Provide global leadership for the strategy, governance, and continuous improvement of Computerized Maintenance Management Systems (CMMS) across the manufacturing network. Job Description About the role: Provide global leadership for the strategy, governance, and continuous improvement of

Takeda Pharmaceuticals  1 day ago
USDM Life Sciences jobs

Risk Assessment/Technical Document Specialist The Risk Assessment/Technical Document Specialist serves as a subject matter expert across both IT systems and data integrity for a Takeda quality control lab systems engagement, ensuring solutions are compliant, inspection ready, and operationally

USDM Life Sciences  1 day ago
LanceSoft jobs

Risk Assessment / Technical Document Specialist This role will serve as a subject matter expert across both IT systems and data integrity, ensuring solutions are compliant, inspection-ready, and operationally efficient. 12 Month contract with potential to extend.

LanceSoft  1 day ago
Ardelyx, Inc. jobs

Executive Director, QMS And Digital Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create

Ardelyx, Inc.  1 hour ago

Manager, QC Instrument Specialist - Devens, MA Attention Military Affiliated Job Seekers - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military,

National Guard Employment Network  2 days ago
Vericel jobs

Director, Facilities & Engineering At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific

Vericel  1 hour ago
Vedanta Biosciences jobs

Head Of Quality (Vice President) Cambridge, MA (hybrid) Vedanta Biosciences is a late-stage biopharmaceutical company developing medicines for the treatment of gastrointestinal diseases. The companys lead asset is a potential first-in-class oral therapy, VE303, in a

Vedanta Biosciences  3 days ago
US Tech Solutions jobs

Job Title Duration: 12 months (potential to extend) Onsite Expectations: For onboarding and training for the first few weeks should plan to be onsite 4-5 days a week. After onboarding and starting working on projects, it

US Tech Solutions  1 hour ago

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