Scientist II or III - Analytical Chemist Metrology Support - FSP
Scientist II or III - Analytical Chemist Metrology Support - FSP
Posted 5 days ago
SENIORITY
Senior
About the role
- B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline
- Scientist 2 B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience
- Scientist 3 B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience
- Experience working within a regulated (GMP) laboratory
- Experience maintaining, operating, and troubleshooting laboratory equipment including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible spectroscopy (UV-Vis), dissolution systems, and other specialized computerized systems.
- Familiarity with standalone computer system GMP validation requirements
- Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks
- Capable of working independently under moderate supervision
- Strong verbal and written communication skills
- Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators
- Familiarity with authoring relevant instrument standard operating procedures (SOPs)
- Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation
- Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships
- Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities
- Participate in computer system validation activities associated with new or upgraded equipment or software packages
- Support the purchase, installation, and equipment qualification of new laboratory equipment
- Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support
- Originate and progress Notice of Event (NOE) and Change Management (CM) records
- Perform and document investigations and assist in developing/implementing CAPA plans
- Represent the laboratory on all aspects of laboratory equipment during audits
- Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures
- About Parexel
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