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
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.
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
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.
Title: Validation Engineer – Quality Assurance | Cell Therapy | GMP Location: Westborough, MA 01581 (Onsite) Job Duration: 06 Months Contract + (Possibility of extension) Working Environment Choose one of the first two statements below to describe
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
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
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
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
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.
Manager, QC Instrument Specialist Challenging. Meaningful. Life-changing. Those arent 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
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. Join the PPD clinical research business of Thermo Fisher Scientific, where our
About ECI ECIs mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and
Job Title: CSV / CQV Engineer Location: MA Experience:6years Resource:2 SLA:By EOD Duration: 6 months Start Date: August 31st JOB Description: Seeking experienced CSV / CQV Engineers to provide onsite validation support within a regulated biopharmaceutical manufacturing
Position: CSV / CQV Engineer Location: Massachusetts Duration: Long Term Job Overview We are seeking a CSV / CQV Engineer to support validation activities in a regulated biopharmaceutical manufacturing environment. The role will focus on Computer System Validation (CSV)