Manager, RA and QA @ Meridian Life Science Inc. (January 1998 - January 2012)
Manager RA and QA @ Immunotech Inc (October 1994 - June 1998)
Manager, RA and QA @ Perseptive Biosystems (June 1993 - September 1994)
Manager, RA and QA @ (June 1991 - June 1993)
Director, RA and QA @ Ventrex Laboratories (January 1983 - June 1991)
Manager, Regulatory Affairs @ Delmed Inc. (September 1980 - December 1982)
Regulatory Affairs Coordinator @ (August 1975 - August 1980)
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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