- Sumitomo Pharma (Phoenix, AZ)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... interpret drug metabolism and ADME data. + Direct activities of contract research laboratories (CROs), including metabolism and bioanalytic activities and assuring… more
- Catalent Pharma Solutions (Kansas City, MO)
- …Product Lead** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer,...related technical discipline; A minimum of 15 years of Pharmaceutical Manufacturing experience may be substituted for the degree… more
- Charles River Laboratories (Northridge, CA)
- …the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and ... SME for Technical Operations, the Director is responsible for ensuring compliance of all technical operations with applicable Standard Operating Procedures (SOPs),… more
- Curia (Albuquerque, NM)
- …operation, providing technical support for validated systems. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to...of Validation related issues that may have a regulatory compliance or financial impact. + Responsible for providing leadership… more
- Eurofins (Auburn, ME)
- …industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the ... and provides leadership and direction as needed. Responsible for ensuring compliance and integration of facility operation with corporate and regulatory policies… more
- Sanofi Group (Cambridge, MA)
- …(in vitro biology and in vivo pharmacology), Research lab operations, and pharmaceutical research experience in agile settings. They will maintain quality standards ... Provide strategic leadership in establishing and managing external partnerships and Contract Research Organization (CRO) relationships. Oversee the full lifecycle of… more
- Robert Half Finance & Accounting (Meriden, CT)
- …the unique financial, regulatory, and operational challenges in manufacturing or pharmaceutical environments. The successful candidate will be a proactive partner to ... costs and support product costing and variance analysis + Ensure compliance with internal controls, corporate policies, and external regulations + Coordinate… more
- Robert Half Technology (Bridgewater, NJ)
- …ability to manage cross-functional support initiatives. Prior experience in the pharmaceutical or biotechnology industry is highly desirable. Key Responsibilities: + ... in system upgrades, patching, and change management processes. + Ensure compliance with relevant regulatory and data governance standards, especially within a… more
- Robert Half Technology (South Plainfield, NJ)
- …or pharmaceutical industries, with knowledge of relevant regulatory and compliance frameworks (eg, GxP, HIPAA, FDA). + Familiarity with private equity ... IT projects related to mergers, acquisitions, and divestitures within the pharmaceutical industry. This position offers an exciting opportunity to lead complex… more
- Honeywell (Baton Rouge, LA)
- …with quality and regulatory standards. The GMP QA Manager also monitors Contract Manufacturing Organizations (CMOs) ensuring compliance of the manufacturing, ... packaging and analytical testing of pharmaceutical dosage forms and drug substances. They also identify...forms, and work instructions + Performs Independent audits for compliance to policies and procedures: on paper vs. practice… more