- 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
- 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
- Gilead Sciences, Inc. (El Segundo, CA)
- …work on innovative T cell therapy for cancer treatment. The Cell Therapy Specialist will be responsible for cell culture media preparation, cell processing and cell ... expansion in a cGMP manufacturing facility. **Responsibilities:** . Perform all tasks associated...with Product Sciences and Quality . Assist in the development of standard operating procedures, batch records, deviations and… 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
- Merck (Wilson, NC)
- …investigations, approve investigations, Annual Product Reviews, regulatory document reviews, process change request activities, SOP development and review, ... general direction of the Associate Director, Wilson Quality Operations, the Specialist is primarily responsible for support of Quality Assurance activities within… 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
- Bausch Health (Bridgewater, NJ)
- …of improving people's lives with our health care products. The **Senior Specialist , External Manufacturing Quality** plays a crucial role in upholding compliance ... devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements. With a keen eye… more
- Boehringer Ingelheim (Athens, GA)
- …to assess the quality / compliance of current Good Manufacturing Practice ( cGMP ), applicable regulations, and applicable company policies and procedures. May support ... contractors on behalf of the BI manufacturing world, including Operations, Development , Biopharma, and Animal Health. Ensures corrective measures are implemented.… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Analytical Quality Assurance Specialist Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION ... New Biological Entities (NBEs'), with eight molecules in various stages of clinical development . Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US… more
- Catalent Pharma Solutions (Greendale, IN)
- **Quality Assurance Specialist II** **Position Summary** Welcome to Greendale, Indiana! Greendale is one of two gummy technology development and manufacturing ... plant-based pectin gummies for nutritional supplements and nutraceuticals. With extensive development and manufacturing expertise and a wide range of flavors,… more
- Merck (West Point, PA)
- …areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development , Technical Services, Utilities and Validation. The ... + Reports to and receives supervision from a Senior Specialist or Associate Director. On routine process ...Experience and Skills:** + Minimum one (1) year of cGMP , technical/mechanical services experience. + Good interpersonal skills including… more
- Actalent (Brownsburg, IN)
- …as needed Skills: GMP, Laboratory, Quality Control, Chemistry, Six sigma, Process improvement, Batch Record, cGMP , Cyclotron, Particle Accelerator, Sample ... HIRING NOW: Lead Sr. QC Specialist for a leading Biotech company in Indianapolis!...EPA, chemical, waste disposal, etc. * Adhere to SOPs, cGMP requirements, company policies, regulatory requirements * Regulatory compliance:… more
- Boehringer Ingelheim (St. Joseph, MO)
- …an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development , and delivery of our products to our patients and customers. Our ... reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Production Execution Systems assists the supervisor in coordinating the… more
- Charles River Laboratories (Memphis, TN)
- QC Specialist III Microbiology Req ID #: 222403 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to ... assist in the discovery, development and safe manufacture of new drug therapies. When...you can feel passionate about. **Job Summary** The QC Specialist III will be responsible for participating and leading… more
- Merck (Rahway, NJ)
- … knowledge capture, and troubleshooting equipment with the aim of advancing process development , aiding technology development , and supplying Active ... The Operations Specialist role at the Associate Specialist level will serve as a process ...of new manufacturing technology/processes, training opportunities for improved manufacturing process development and seamless tech transfer to… more
- Boehringer Ingelheim (St. Joseph, MO)
- **Description** The Specialist , Automation should have knowledge of AVEVA System Platform DCS and process integrations to our upstream and downstream of the ... manufacturing personnel and supervision on support the antigen manufacturing process equipment, work methods, troubleshooting techniques and continuous improvement… more