David Cromwick

Vice President of Quality and Regulatory

We found the following information about David Cromwick at Bruker Biospin, where this professional has worked as a Vice President of Quality and Regulatory since 2018. David's total work experience is over 13 years, during which time the professional had at least five jobs at different companies to develop skills. David studied at the Columbia University In the City of New York. David currently lives in Saugus, Massachusetts. You can contact with David by searching for phone or email address or find further info by requesting access to this expert's further details.
Name variants:
Daved Cromwick, Dayvid Cromwick, Dave Cromwick, Davey Cromwick, Davie Cromwick, Davy Cromwick
Last updated Mar 17, 2024

Contact Information

Last Update
Jul 10, 2022
Email
da**@beaver-visitec.com, da**@bruker.com
Location
Saugus, MA
Company

Workplace

Bruker BioSpin
Vice President of Quality and Regulatory

Billerica, MA

Industry

Biotechnology, Sale and service of scientific instruments., Whol Professional Equipment, Surgical & Medical Instrument Mfg

Work History

Vice President of Quality and Regulatory

15 Fortune Dr, Billerica, MA 01821
from Jan 2018

Director of Quality

40 Manning Rd, Billerica, MA 01821
Bruker Daltonics is a leading global developer and manufacturer of innovative scientific instruments that address the rapidly evolving needs of a diverse array of life sciences customers. Ou...
from Jan 2016

Director, Quality Assurance and Compliance

22 Cherry Hill Dr, Danvers, MA 01923
Dec 2012 — Dec 2015

Vice President of Quality and Regulatory

Waltham, MA
Aug 2010 — Dec 2012

Director of Quality

Bd
1 Becton Dr, Franklin Lakes, NJ 07417
May 2002 — Jul 2010

Occupations

Executive
Vice President
Scientist
Biotechnology Professional
Director
Chief Executive
Biologist
Biological Scientist
Operations Manager

Skills

Iso 13485
Medical Devices
Iso 14971
Quality System
Fda
Capa
Design Control
Quality Assurance
Validation
Six Sigma
Lean Manufacturing
Continuous Improvement
Fmea
Gmp
Iso 9000
V&V
Design of Experiments
Minitab
Regulatory Affairs
Dmaic
Spc
Root Cause Analysis
U.s. Food and Drug Administration
Iso
Supplier Quality
Cqe
21 Cfr
Quality Auditing
Change Control
Ce Marking
21 Cfr Part 11
Fda Gmp
Cqa
Value Stream Mapping
Iso Standards
Corrective and Preventive Action
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