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
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
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.
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
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
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
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
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
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
Lead Facilities Maintenance Technician Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day,
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
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
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.
Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values
Sr Lead QA Analyst A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service
SR Lead QA Analyst A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service
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