JobRx, Inc. is seeking an APQR Program Lead to oversee annual product quality reviews, merging data evaluation with engineering controls to ensure products meet safety and quality standards. The role leads statistical trending, data collection, and the drafting
Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of
Senior Specialist, QA Program Management Syracuse, NY We are LOTTE BIOLOGICS! Delivering Therapies That Enable a Healthier World. A new company, built on 80 years of tradition. We embody our core values of being Inspired by Science,
Portfolio Business: Huber Engineered Materials J.M. Huber Corporation is one of the largest privately held, family-owned companies in the United States. Established in 1883, we are a diversified, global supplier of specialty and commodity chemicals, hydrocolloid
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Position Summary The person in charge of QC is responsible for leading all Quality Control activities at the Alexion Georgia Manufacturing Facility in Bogart, including oversight of QC operations, personnel, and budget. The role includes responsibility
Job SummaryThe QA Compliance Specialist works with the Compliance Management Team to Identify and correct cGMP inadequacies at the Production Unit, as well as, helping to develop and implement Quality Systems designed to maintain a high
Job Description General Summary: The Analytical Science and Technology (AS&T) Principal Scientist, Separation Method Expert, will be responsible for providing scientific and technical expertise within and across functional areas for late-stage & commercial methods and vendor
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
Associate Director Quality Assurance Department: Quality Reports To: Vice President, Regulatory Affairs, Drug Safety, Quality FLSA Status: Exempt Job Type: Full-time Location: Raleigh, NC (hybrid role) The Associate Director, Quality Assurance is responsible for supporting the
This job is with Gilead Sciences Inc., an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Gilead, were creating
Overview Create a future where DNA is no longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We
Quality Control Manager The person in charge of QC is responsible for leading all Quality Control activities at the Alexion Georgia Manufacturing Facility in Bogart, including oversight of QC operations, personnel, and budget. The role includes
Senior Manager, ExM Quality Analytical This role is 100% Onsite. Person can work from either the New Brunswick or Summit West site. Local Candidates Only. Work Schedule: Mon - Fri, Business Hours. *When submitting candidates, please
Quality Systems Associate Director The Quality Systems Associate Director supports strategic design of and ensures tactical execution of quality systems, risk management, and quality culture across the Vertex Cell and Gene Therapy (VCGT) organization. The role
Senior Manager Hybrid Role New Brunswick, NJ Work Schedule: Mon - Fri, Business Hours Business Unit / Department: External Manufacturing Quality Principle Objective of Position: This role is a development opportunity for 12 months to gain
Senior Manager, Quality Systems Hi, were Supergoop! Since 2005, weve been changing the way the world thinks about sunscreen. Today, were as committed as ever to creating feel-good sunscreen that youll really want to wear. Because
Product Quality Lead (PQL) At Gilead, were creating a healthier world for all people. For more than 35 years, weve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapies that
Position Summary The Global Biologic Stability (GBS) team manages the stability programs for Clients commercial biologics Drug Substances and Drug Products. The global stability program supports all internal and external manufacturing sites. The Stability Senior Scientist reports to
Quality Control Manager STAQ Pharma is a 503B Outsourcing Facility located in Denver, Colorado. STAQ Pharma produces sterile injectable medications for adults and pediatric patients, compounded under cGMP standards. STAQs ownership and board are composed of