- Merck & Co. (Durham, NC)
- …implementation. Preferred Experience - Skills - Knowledge Experience with on-the-floor cGMP manufacturing support Authored complex process change control or ... Job DescriptionWe are seeking a Growth and Improvement minded Validation Specialist that can help drive our Strategic Operating Priorities. Invent - Pursue the Most… more
- Merck & Co. (Rahway, NJ)
- …the broader Enabling Facilities Automation Team supporting facility operations, process development activities, compliance investigation, change management and ... of new manufacturing technology/processes, training opportunities for improved manufacturing process development and seamless tech transfer to commercial… more
- Merck & Co. (Rahway, NJ)
- …of new manufacturing technology/processes, training opportunities for improved manufacturing process development and seamless tech transfer to commercial ... supply facility.Experience with small molecule drug substance and/or biologics process development .Experience in supporting compliance investigations and change… more
- Merck & Co. (Rahway, NJ)
- … knowledge capture, and troubleshooting equipment with the aim of advancing process development , aiding technology development , and supplying Active ... of new manufacturing technology/processes, training opportunities for improved manufacturing process development and seamless tech transfer to commercial… more
- Catalent (Manassas, VA)
- POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the production ... or contractors inside the production plant are following our cGMP and execute corrective actions when needed. Assist the...nutraceuticals, as well as small batch lozenges. With extensive development and manufacturing expertise and a wide range of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...for clinical trials and commercial operation in a controlled cGMP environment. Reviews, inspection, and disposition of all incoming… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … process flow diagrams as well as protocol and reports from development . Support the implementation of manufacturing and process improvement strategies ... and Quality to ensure seamless implementation of technical transfer activities and/or process improvements. Work closely with the development organization to… more
- University of Southern California (Los Angeles, CA)
- …in the university's current Good Manufacturing Practices ( cGMP ) facility. The Process Development Specialist is responsible for developing procedures and ... Process Development SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Process - Development - Specialist \_REQ20145450/apply) Keck School… more
- Gilead Sciences, Inc. (Frederick, MD)
- …to join us in this mission? We are seeking a highly motivated, Cell Therapy Specialist to join our newly formed Cell Therapy Manufacturing team at Kite's brand new, ... Cell Therapy facility in Frederick, Maryland. The Cell Therapy Specialist will perform and/or verify all tasks associated with...unique, innovative immunotherapies? Do you have a background in cGMP manufacturing? If the answer is yes, we'd like… more
- Unither Pharmaceuticals (Rochester, NY)
- …company SOPs and industry standards. Provides Quality oversight to the drug development process , including safety, toxicity and regulatory compliance and the ... Quality Specialist - Development & Validation Who...maintain partnerships with internal teams and external organizations supporting development , technology transfer, process validation, and commercialization… more
- Merck (Durham, NC)
- …implementation. **Preferred Experience | Skills | Knowledge** + Experience with on-the-floor cGMP manufacturing support + Authored complex process change control ... **Job Description** We are seeking a Growth and Improvement minded Validation Specialist that can help drive our Strategic Operating Priorities. + Invent | Pursue… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …completion of associated operations/documentation, and assisting in the monitoring of cGMP compliance. As a Specialist of External Manufacturing (DS/FDS/API), ... We are currently looking to fill a Specialist position within the New Modalities External Manufacturing...or business partners. + Leads a sub-team in continuous process improvements, system/equipment implementation and/or strategy development .… more
- Cardinal Health (Fort Lauderdale, FL)
- …Health's Nuclear and Precision Health Solutions organization tasked with the development and technology transfer of radiopharmaceutical products into and among our ... quality functions at the PET manufacturing site, such as: + Handles cGMP documentation review related to product release, facilities and equipment, material… more
- Kedrion Biopharma, Inc. (Melville, NY)
- …in hematology, immunology, neurology, and transfusion medicine. The Quality Operations Specialist has a robust understanding of applicable CGMP regulations ... Kedrion Biopharma is a biopharmaceutical company specializing in the development , production and distribution of plasma-derived products. Kedrion has been producing… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- Job Title Sr. Process Safety Specialist - Onsite Requisition JR000014049 Sr. Process Safety Specialist - Onsite (Open) Location St. Louis, MO (Pharma) - ... and processes to continually improve the organization's safety culture. The Sr. Process Safety Specialist will directly support site needs for developing,… more
- ThermoFisher Scientific (Plainville, MA)
- …Plainville) business unit of Thermo Fisher Scientific. At VVS Plainville, we deliver process development through commercial supply and offer the expertise and ... genetic, rare, and otherwise untreatable diseases. **Discover Impactful Work:** The Procurement Specialist III reports to the Sr. Manager Procurement into the Viral… more
- Merck (West Point, PA)
- **Job Description** The Senior Specialist is an experienced individual contributor. **ACCOUNTABILITY** As a member of the Engineering, Maintenance, & Utility ... in compliance with GMP, safety, and environmental regulations. Responsible for the development of objectives and projects and upon approval, implements by self or… more
- National Institutes of Health (Montgomery County, MD)
- …Affairs-Facilities organization within ORSC provides regulatory support for the various cGMP and compounding facilities on campus. Support includes guidance in ... preventative maintenance, will aid in FDA Inspections of facilities, aide in development of Quality Systems, and responses to audits. Responsibilities As a GS-0601… more
- ThermoFisher Scientific (Cambridge, MA)
- …strong communication, leadership, technical and operational skills to join our growing Process Development team. This position is focused on service delivery ... related field, preferred **Experience:** * 1+ years' experience in a process development / manufacturing environment preferred. **Knowledge, Skills, Abilities**… more
- Kelly Services (Irving, TX)
- **QC Specialist II - Irving, TX (Pharma)** **Are you a detail-oriented scientist with a passion for quality? Do you thrive in a fast-paced environment where your ... a leader in analytical testing services. We are seeking a highly motivated QC Specialist II to join our growing team. **About Company:** This laboratory is a dynamic… more
