1998 -2012 Manager, RA and QA @ Meridian Life Science Inc.
1994 -1998 Manager RA and QA @ Immunotech Inc
1993 -1994 Manager, RA and QA @ Perseptive Biosystems
1991 -1993 Manager, RA and QA @
1983 -1991 Director, RA and QA @ Ventrex Laboratories
1980 -1982 Manager, Regulatory Affairs @ Delmed Inc.
1975 -1980 Regulatory Affairs Coordinator @
Jim Champlin Education
Northeastern University
Post graduate studies (Pharmacology)
1977-1978
Tufts University
BS (Biology)
1971-1975
Jim Champlin Skills
Pharmaceutical Industry
Validation
Purification
Immunoassays
Cell Culture
Strategic Planning
ISO
IACUC
Leadership
Event Planning
CAPA
Diagnostics
Chromatography
Product Development
CMC Regulatory Affairs
Lifesciences
Quality Assurance
Medical Devices
FDA
Marketing
Conjugation
Life Sciences
Internal Audit
Auditing
Hardware Diagnostics
Biotechnology
Quality Control
Regulatory Affairs
Aseptic Processing
Supply Chain Quality Monitoring
ISO 13485
GMP
Management
Immunology
Jim Champlin Summary
Jim Champlin, based in Buxton, ME, US, is currently a Director, Quality, Safety, Health, Infrastructure and Environment at Maine Standards Company LLC. Jim Champlin brings experience from previous roles at Miltenyi Biotec, Meridian Life Science Inc., Immunotech Inc and Perseptive Biosystems. Jim Champlin holds a 1977 - 1978 Post graduate studies in Pharmacology @ Northeastern University. With a robust skill set that includes Pharmaceutical Industry, Validation, Purification, Immunoassays, Cell Culture and more.
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