- United Therapeutics (Silver Spring, MD)
- …and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Senior Validation Specialist or Engineer, Equipment will perform ... in a scientific field and 5+ years of relevant validation experience in a pharmaceutical /cGMP environment +...colleagues and management cross-functionally, to provide the status of validation activities, to collaborate with peers, senior … more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Glenmark is actively seeking a Senior Validation Specialist ... Sr. Validation Specialist , Pharmaceuticals - Monroe,...must have a Master-s Degree (or US equivalent) in Validation Engineering, Pharmaceutical Chemistry, Chemistry or … more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Senior Specialist , MSAT Department: Validation Location: Monroe, NC START YOUR APPLICATION ... (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req\_id=2981422&source=2981422-CJB-0) Position Summary: Glenmark is actively seeking a Senior Specialist , MSAT to join the… more
- Unither Pharmaceuticals (Rochester, NY)
- Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and ... and Capsules. It has more than 280 employees. Your role Reporting to the Senior Manager, Engineering, JOB SUMMARY: Manages validation projects or multiple … more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …Validation department at Regeneron is adding to their team! The **QA Validation Specialist - External Partners** coordinates the equipment, systems, and ... + Presents project and program status and metrics to Senior Management. Act as Technical Subject Matter Expert (SME)...of experience required for each level: + Associate QA Validation Specialist : 0-2 years + QA … more
- Takeda Pharmaceuticals (Social Circle, GA)
- …true to the best of my knowledge. **Job Description** **About the role** As a Senior Quality Assurance Specialist , you will be on site to provide Quality ... OOR, Protocols authored by QC organization. + Approve Analytical Method Validation /Transfer Protocols and Reports + Participate in problem solving sessions and… more
- Regeneron Pharmaceuticals (Troy, NY)
- …Associate Specialist - 0-2 years + Specialist - 2+ years + Senior Specialist - 5+ years May substitute proven experience for education requirement. Level ... We are currently looking to fill a Quality Compliance Specialist (Complaints) position. This position maintains site compliance of operations focused primarily on… more
- Unither Pharmaceuticals (Rochester, NY)
- Metrology Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify ... Capsules. It has more than 280 employees. Your role Reporting to the Senior Manager, Engineering, Validation & Metrology, Maintains the calibration group's… more
- Charles River Laboratories (Malvern, PA)
- Computer Systems Validation Specialist Req ID #: 221491 Location: Malvern, PA, US, 19355Horsham, PA, US, 19044Wayne, PA, US, 19087Rockville, MD, US, 20850 For 75 ... required. ⦁ Report any non- compliances of Quality Management System with respect to validation to the Senior Management. ⦁ Identify plan and schedule project… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …2+ years of relevant experience; or an equivalent combination of education and experience Senior Analytical Specialist I: BS/BA, or related field and 4+ years of ... Regeneron is currently looking for an Analytical Development Specialist position with a 1st shift, Tuesday-Saturday, 8am-4:30pm schedule. This technical lead… more
- Stantec (Albany, NY)
- Commissioning/ Validation Specialist - ( 240000E0 ) **Description** Stantec Buildings is on a mission to become the world's leading integrated design practice. ... group for an enthusiastic, diligent commissioning engineer / specialist . In this role you will prepare and implements...intent and client requirements. Working under the guidance of senior commissioning/ validation staff, you will work on… more
- Takeda Pharmaceuticals (Lexington, MA)
- …and Business Solutions Organization. As a key team member in COBS, the Senior Analyst, CRM Business Solutions will be engaged in transformative initiatives. They ... ensuring its continued success in a rapidly evolving marketplace. The Specialist , Field Platforms is responsible for establishing and maintaining excellence within… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …of relevant experience for each level: + Associate QA Specialist - 2+ years + QA Specialist - 4+ years + Senior QA Specialist - 6+ years May substitute ... We are currently looking to fill a Quality Assurance Specialist position to support the Manufacturing Execution System (MES). This position will support a cross… more
- Regeneron Pharmaceuticals (Troy, NY)
- …while following GAMP 5 guidelines + Supporting manufacturing, engineering, and validation projects + Providing support to process control and process monitoring ... work with a career goal of becoming a domain specialist . + Have a knack for compiling documentation and...Engineer: BS with 2+ years of relevant experience + Senior Automation Engineer: BS with 5+ years of relevant… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Senior Specialist Medical Device and Combination Product (MDCP) engineer is a key technical leader of regulatory and ... development, and package development for medical devices, combination products, and pharmaceuticals . The person in this position participates in high impact,… more
- Bausch Health (Bridgewater, NJ)
- …our mission of improving people's lives with our health care products. The ** Senior Specialist , External Manufacturing Quality** plays a crucial role in ... Cosmetic, and Medical Device regulated environment. Reporting directly to the Senior Manager of Quality, this position collaborates closely with External… more
- United Therapeutics (Eden Prairie, MN)
- …to help patients with liver and kidney disease. How you'll contribute The Senior QC Specialist is responsible for completing raw material certificate review ... for transplantation. We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...the team + Perform method transfer, method qualification, and validation activities + Author and approve SOPs, test methods,… more
- Novo Nordisk (Clayton, NC)
- …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
- Novo Nordisk (Clayton, NC)
- …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
- Mayo Clinic (Rochester, MN)
- …provides the resources you need to succeed. **Responsibilities** The Biomanufacturing Senior Specialist supports the development and production of ... biotherapeutics via approved standard operating procedures (SOPs) and product validation for FDA-regulated, CGMP manufacturing operations. Primary responsibilities include… more