- Grifols Shared Services North America, Inc (Clayton, NC)
- …(chromatography, ultrafiltration, nanofiltration), steam sterilization, Clean-In-Place systems and processing vessels. ** Sr . Validation Specialist I:** The ... requires a minimum of 2 years' experience in the pharmaceutical industry ** Specialist II** - Requires a...Sr . Validation Specialist I is responsible for conducting validation … more
- Astellas Pharma (Westborough, MA)
- ** Senior Validation Specialist , Quality Assurance** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? ... you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries...AIRM is headquartered in Massachusetts. Astellas is announcing a ** Senior Validation Specialist , Quality Assurance**… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …Chemistry, or Life Sciences and the following years experience for each level: + Staff QA Validation Specialist : 10+ years + Sr . Staff QA Validation ... QA Validation department is hiring! The QA Validation Specialist validates and qualifies equipment, systems,...+ Presents project and program status and metrics to Senior Management. Act as Technical Subject Matter Expert (SME)… 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
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Senior Specialist , MSAT Department: Validation...MSAT to join the growing team in Monroe. The Sr . Specialist , MSAT will provide technical expertise ... of equipment & facility qualifications, computer system validations, and cleaning validation + Hands-on experience in Manufacturing Operation of Sterile /Parenteral… more
- Boehringer Ingelheim (Barceloneta, PR)
- **Description** This Automation Specialist will support Boehringer Ingelheim AH Puerto Rico site to ensure that the local business own computer systems and ... Business Own systems. + Support the site compliance by ensuring computer validation requirements through the system and equipment end-to-end SDLC process, including… more
- The Hershey Company (TN)
- *Location*: Memphis, TN * Summary:* Under Minimal guidance, the Food Safety Compliance Specialist 's primary role is to coordinate efforts to achieve and maintain the ... develop corrective/preventive actions, lead 3rd party audits, and complete required validation and verifications of the system. The Practitioner will deliver… more
- Quality Consulting Group (Juncos, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... + Technical writing knowledge + Organization and Communication skills + Process Validation and Computer software validation knowledge + Experience with Trackwise… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …10+ years industry relevant experience, 9+ years with MS or 4+ years with PhD. + Sr Staff Specialist requires a minimum of a BA/BS in any physical or biological ... **Summary:** The External Manufacturing Principal Specialist provides technical and process support for all aspects of clinical and commercial parenteral drug… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …and the following amounts of relevant experience for each level: + Quality Compliance Specialist : 2+ years + Sr . Quality Compliance Specialist : 5+ years ... We are currently looking to fill a Compliance Specialist position supporting Supplier Quality. This position maintains site compliance activities related to supplier… 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
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior IT Business Application Manager (Clinical Supply Chain) Date: Sep 12, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva ... Pharmaceuticals Job Id: 57687 **Who we are** Together, we're...**The opportunity** As the IT SHM (Stakeholder Management) lead specialist in the clinical supply chain, you will play… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and cost-effective processes for the manufacture of new synthetic molecule pharmaceuticals , along with methods for achieving and controlling high standards of ... will be recognized as a technical resource/expert within SMPD and across Pharmaceutical Sciences and utilize his/ her technical expertise to contribute across… more
- Mentor Technical Group (Juncos, PR)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... assignments in related fields. 6. Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …assessing timelines, and ensuring resolution per the timelines. This position supervises MSAT Senior Specialist and MSAT Specialist (I, II, and/or III). ... Manufacturing Science and Technology (MSAT) - Monroe, NC Department: Validation Location: Monroe, NC START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req\_id=3142637&source=3142637-CJB-0) Provide… more
- Regeneron Pharmaceuticals (Troy, NY)
- …following GAMP 5 guidelines + Supporting small 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...level: + Automation Engineer: BS with 2+ years + Senior Automation Engineer: BS with 5+ years + Principal… more
- Bausch Health (Bridgewater, NJ)
- …mission of improving people's lives with our health care products. The ** Senior Specialist , External Manufacturing Quality** is responsible for maintaining ... product lifecycle for NDA, ANDA, OTC, Medical Devices, and combination products. The senior specialist is also responsible for managing the electronic document… more
- Cambridge Isotope Laboratories, Inc. (Xenia, OH)
- …Isotope Separations (CIS) has an outstanding opportunity for an experienced Quality Assurance Senior Specialist based onsite in our Xenia, OH location. CIS is ... located at its CIS facility. Summary: Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance… 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
- Bausch + Lomb (Woodruff, SC)
- …the advancement of eye health in the future. **Purpose of Job:** A senior level Quality professional that supports the development and maintenance of site-specific ... Non-conformance/CAPA, Change Control, Document Management, Records Management, Data Integrity, Validation , Risk Management, Training, Customer Service Complaints, Supplier Management,… more