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International Regulatory Affirs Specialist
GYRUS ACMI
-US - MA - Southborough
BS/BA required, preferably in engineering or life sciences. Regulatory affairs experience in the Medical Device industry is mandatory [minimum 3-5 years preferred]. ...
Feb-07-2012
Principal Regulatory Affairs Specialist
Boston Scientific
-US - MA - Natick
Preferred Qualifications Candidate should have strong experience in the combination products space, particularly dealing with CMC sections and CDER. Additional require...
Jan-30-2012
Entry/ Mid Level Regulatory Affairs Specialist
Boston Scientific
-US - MA - Marlborough
• Bachelor’s degree or equivalent work experience, preferably in a scientific or technical discipline. • 0 – 4 years Regulatory Affairs experience, medical industry experien...
Jan-30-2012
Senior/ Principal Regulatory Affairs Specialist
Boston Scientific
-US - MA - Marlborough
Qualifications: • Bachelor’s degree or equivalent work experience, preferably in a scientific or technical discipline. • Professional certification(s) preferred. • 5-8 years Re...
Jan-30-2012
Associate, Regulatory Affairs
Momenta Pharmaceuticals
-US - MA - Cambridge
Momenta Pharmaceuticals is seeking an Associate, to join our Regulatory Affairs team. The Associate will be the primary lead to oversee operational and logistical aspects related to the Compan...
Jan-27-2012
Medical device QMS auditors in US NE
Intertek
-US - MA - Home-based - US North East (MA, CT, NY, NJ, PA)
Required: • Relevant formal education equivalent to a 4 year college/university degree in the U.S. • Previous work experience in the medical device industry (at least 10 years) • Wil...
Jan-25-2012
CMC Regulatory Manager
Ipsen
-US - MA - Milford
Education: BS in a scientific discipline (biology, chemistry, pharmacy) Experience • 7 + years of pharmaceutical experience with at least 5 years in the preparation and ...
Jan-23-2012
Manager/ Sr. Manager of International Regulatory Operations (Ex-US)-- Biologics
Trident Search LLC
-US - MA - Cambridge
Experience and Background Candidate will need a minimum of 5-10 years of directly related regulatory international bio/pharmaceutical experience (particularly EU but other geographic...
Jan-13-2012
View Map of US - MA - Cambridge
Regulatory Affairs Scientist I/ II (Needham, MA)
Celldex Therapeutics
-US - MA
Required Skills: Scientific understanding of the FDA and ICH biotechnology-derived medicinal product drug regulations (and global regulatory requirements a plus) Experience with IND, ...
Jan-13-2012
View all Celldex Therapeutics jobs
Director of Regulatory Affairs & Quality Assurance
Confidential
-US - MA
The successful candidate will bring: a) Successful track record in the medical device industry. Knowledge of Class III regulatory requirements and/or cardiac exposure is a plus; b) Worki...
Jan-12-2012
