Job Description SummaryWe are seeking a Lead QA Specialist – New Product Implementation to provide Quality Assurance leadership for the introduction of new products across a global external manufacturing network. In this role, you will lead
The Product Quality Manager is responsible for providing quality leadership, oversight, and decision support throughout the product development lifecycle of bioprocess products and solutions. This role ensures that product designs, specifications, materials, manufacturing processes, verification and
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
ABOUT US Bonfiglioli is a worldwide designer, manufacturer and distributor of a complete range of gearmotors, drive systems, planetary gearboxes and inverters, which satisfy the most challenging and demanding needs in industrial automation, mobile machinery and
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.
Location(s) Shanghai, Shanghai Company Molex Career Field Research & Development/Sciences Job Number 192649 What You Will Do 1.Review and interpret customer design requirements from Marketing, Sales or Customer drawings or specifications. 2. Provide preliminary design feasibility
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
• Participate TFC and Contract Review meeting to identify potential supplier risks • Responsible to define CLD according to ASM, implement necessary audit to supplier process at different phase, such as PPAP trial run, run at
This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, well invite you for an interview. If
ABOUT QUINCE Founded in 2018, Quince was built to challenge the idea that nice things have to cost a lot. Our mission is simple: to make really high quality essentials for really low prices, produced fairly
Job Description SummaryGE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join
Typical Accountabilities Responsible for establishing study and trial level V2V process. Establish cell therapy site qualification criteria and conduct technical on-site assessment. Responsible for developing V2V related study and trial documents, creating apheresis and product administration
About AkzoNobel Since 1792, we’ve been supplying the innovative paints and coatings that help to color people’s lives and protect what matters most. Our world class portfolio of brands – including Dulux, International, Sikkens and Interpon
As a Product Quality Engineer at Meta, you will take responsibility to ensure that the product produced in the manufacturing site meets the requirements defined by the team, covering product cosmetic, function, and reliability. You will
Job Description External Manufacturing Large Molecule Drug Substance Technical Lead Our Large Molecule Technical Operations Unit is seeking a highly motivated individual to fill an open Associate Director Technical Operations, to support drug substance manufacture within
ABOUT QUINCE Founded in 2018, Quince was built to challenge the idea that nice things have to cost a lot. Our mission is simple: to make really high quality essentials for really low prices, produced fairly
Your mission Contribution to the Continuous Improvement of the Corporate Midas Pharmaceutical Quality System. Management of international GxP and Regulatory standards during sourcing, development, procurement, manufacturing and supply chain of Drug Substances (IM, API) and Medicinal
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,