Job Summary: Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations and other functional groups as required (e.g. Facilities Engineering, IT, Supply Chain, etc.). Support timely review of events for classification,
Overview: The purpose of a Field Deviation Coordinator is to review deviated items that come back from the field and determine a resolution. Then, effectively communicate, document and rescheduled install date with our customers. Field Deviation Coordinator’s purpose
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
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of
Career CategoryOperations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that
Career CategoryOperations Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of
Deviation Investigator I Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–4:30 PM EST. What you will get: Below you will find a comprehensive summary of
MS&T Specialist – Deviations Investigator Location: Davie, FL Shift: Monday - Friday 8:00am - 5:00pm Duration: 6 months Temp to Perm: Possibility based on workers performance and openings Core Essential skill sets required: 1. This role will
Deviation Investigator – API Manufacturing Location: Rensselaer, NY (Onsite) Duration: Contract Position Summary We are seeking an experienced Deviation Investigator with hands-on API (Active Pharmaceutical Ingredient) manufacturing experience to support investigation and remediation activities within a GMP-regulated manufacturing
Job Title Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations and other functional groups as required (e.g. Facilities Engineering, IT, Supply Chain, etc.). Support timely review of events for classification,
WHO? INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The
divh2Deviations/Capa Manager Quality Systems IV/h2pIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively.
Field Deviation Coordinator The purpose of a Field Deviation Coordinator is to review deviated items that come back from the field and determine a resolution. Then, effectively communicate, document and reschedule install date with our customers. Field Deviation Coordinators
QA Compliance Specialist Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work ScheduleStandard (Mon-Fri) Environmental
Job Title: CMC Synthetics Clinical Manufacturing Leader Location: Cambridge, MA About the Job The Projects and External Technologies team, part of the CMC Synthetics organization within Sanofi R&D, is responsible for the delivery of clinical drug
Azenta Inc. At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and
Job Title: Senior Manager, Manufacturing Compliance Location: Redmond, and Seattle, WA Department: Site MSAT Manufacturing Compliance Reports To: Director, Site MSAT About Us: this is who we are At Just Evotec Biologics, we believe that curiosity