- AbbVie (North Chicago, IL)
- …+ Qualification as QRM facilitator commensurate with responsibility. + May supervise contract validation resources in the timely completion of activities in ... to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes… more
- VTI Life Sciences (Raleigh, NC)
- …end of the year (Initial Contract ) Job Title: Senior Cleaning Validation Engineer Industry: Pharmaceutical Manufacturing Level of Experience: 8+ years ... Validation Engineers to work onsite at our client's pharmaceutical manufacturing facility in the Raleigh, NC area. One...Contract ) Job Description + Looking for a Cleaning Validation Engineer, specifically for drug product parts washers. +… more
- Charles River Laboratories (Memphis, TN)
- …that you can feel passionate about. **Job Summary** Reporting to the Manager Validation , the Validation Engineer II supports the qualification/ validation ... River Laboratories. As a technical resource for GMP regulated facilities, the Validation Engineer II assists primarily in the development and execution of… more
- Curia (Albuquerque, NM)
- …Engineering, or relevant field + Fifteen (15) years relevant experience in pharmaceutical validation (aseptic/sterile product facility) + Experience with ... Senior Principal Validation Engineer in Albuquerque, NM Build your future...technical support for validated systems. Curia is a global contract development and manufacturing organization (CDMO) with over 30… more
- Curia (Albuquerque, NM)
- Validation Analyst II, Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
- Cardinal Health (Indianapolis, IN)
- …waste and inventory reductions. **_Responsibilities_** + Conducts & develops validation and qualification protocols, projects and studies supporting manufacturing ... facility start-up and operation. Validation documentation to ensure products are manufactured in accordance with cGMP, pharmaceutical regulatory agencies,… more
- Catalent Pharma Solutions (Harmans, MD)
- **Lead Specialist, QA Validation & Engineering** Catalent Pharma Solutions is looking to hire a **Lead Specialist, QA Validation & Engineering** to support our ... growing team in Harmans, MD Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture,… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …of experience in Equipment/Facilities/Utilities Qualification experience. + 2+ Computer System Validation (CSV) experience in the pharmaceutical industry. + ... **Senior Validation Specialist** **Position Summary** Catalent, Inc. is a...Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …degree in Science or Engineering required. + 5+ years' experience in the pharmaceutical industry performing cleaning cycle development and validation required. + ... **Senior Cleaning Validation Specialist** **Position Summary** Catalent, Inc. is a...Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is… more
- PCI Pharma Services (Rockford, IL)
- …technical discipline; advanced degree preferred. + Minimum of 5-8 years of validation experience in the medical device, pharmaceutical , or biotech industry. ... to pioneer and shape the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality… more