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
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
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.
Replimune is seeking a Validation Engineer II to join our Framingham site to qualify and maintain facility equipment, utilities, instrumentation and computerized systems in a validated state in accordance with regulatory guidance. You will work with internal customers and
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, we live by our
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, We Live By Our
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
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
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
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
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
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,
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.
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