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.
Process Validation Specialist Location: Torrance, CA | Employment Type: Full-Time Support compliant, reliable manufacturing for clinical and commercial products. At PolyPeptide, we partner with pharmaceutical and biotech companies to support the development and manufacturing of peptide based therapies.
Position Overview The Senior Engineer or Scientist of Process Validation ensures that manufacturing processes meet the validation and regulatory requirements to ensure the process is robust and reproducible under normal operating conditions. This role involves designing, executing, and documenting process validation protocols
With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Standing for full shift Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive
Purpose of the position Foxconn Technology Group, a globally leading electronics manufacturing company, is now hiring a SMT Process Experiment Engineer. Lead failure mode experiment analysis of SMT (surface mounting technology, Consumer Electronics Industry), such as Cross-section/Dye
Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help
More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead
We are a fast-paced business with ambitious growth plans; so if you are dedicated, enthusiastic and always seeking ways to improve, youll enjoy a career with us! Ontic is a leading global aerospace OEM trusted by
Build our future together: Regeneron is seeking a Process Controls & Validation Engineer to join our Process Sciences Drug Product Engineering department. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment)
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Process Controls & Validation Engineer with a strong background in cGMP validation, who can develop sound
General Purpose Perform foundational laboratory, pilot plant, and product development activities in support of process design, process validation, product development, and commercialization initiatives. Perform assigned technical work under guidance, while gaining knowledge of dairy science, product development processes, pilot
This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Bring more to life. Are you
We are actively seeking a Principal QA Process Validation Specialist to provide technical Quality oversight and subject matter expertise for process validation activities supporting aseptically filled drug products. This role is ideal for a Process Validation Engineer or Validation SME with strong technical
Ingenyx, a leading medical device contract manufacturer, is seeking a Manufacturing Engineer for our Jaffrey, NH site to design, develop, and improve manufacturing processes and equipment in a fast-paced environment. The role involves leading cross-functional initiatives,
Massachusetts Health & Hospital Association in Tempe, AZ, is seeking a role to support the development and optimization of medical devices. On-site presence is required to perform hands-on testing and collaborate with cross-functional teams across departments.
Role: Support the development and optimization of medical devices. Responsibilities: Conduct hands‑on testing, prepare technical documents, and collaborate across departments. Qualifications: B.S. or M.S. in a relevant scientific field with 1–3 years of R&D experience in
Process & Validation Project Manager Location: Philadelphia, PA Employment Type: Full-time, mostly onsite About Us Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a