Felix Martinson is a high-level expert, that works in Pfizer main office of which is in 4. as a Director, Combination Products Program since 2018. Felix Martinson has earned professional experience in more than 12 positions at various companies. Felix Martinson went to the Washington University In St. Louis and received education there from 2014 to 2017. Saint Louis, Missouri is the city, where the professional was lastly known to be situated. The professional's email address and phone number can be accessed through SoftwareOfficial by request.
Name variants:
Lix Martinson
Last updated May 14, 2024
Contact Information
Last Update
Jul 14, 2022
Email
fe**@pfizer.com, fe**@hotmail.com, fe**@mallinckrodt.com
Location
Saint Louis, MO
Company
Workplace
Colleagues
Work History
Director, Combination Products Program
New York, NY
Leader for two sites (St. Louis and Columbia, MD) - providing guidance/direction and Quality Unit oversight for Design Control System Life Cycle, the Quality Risk Management Program, and Ris...
from Mar 2018
Quality Director: External Manufacturing, Research and Development, Clinical Quality
Provided Quality oversight and support for Research and Development, External Manufacturing and Clinical Quality functions.
Feb 2017 — Mar 2018
Quality Director Global External Supply
Responsible for leading the US based Global External Supply Quality Organization. Scope includes pre-commercial support for clinical and development projects, acquired asset integration, com...
Jun 1, 2015 — Feb 2017
Acting Vice President Quality Assurance and Regulatory Affairs
Responsible for Quality Assurance, Quality Control, Regulatory Affairs and EHS at a multi-facility biopharmaceutical company.
Jul 2015 — Feb 2016
Manager Plant Quality Ii à   Global External Supply
Responsible for Quality and Compliance related to External Supply chain. Responsible for international projects, due diligence, acquisition/integration activities and all commercial products...
Jun 2013 — Jun 2015
Senior Manager Quality Systems
Responsible for leading the quality systems group at a large API and Finished Dose manufacturing facility. Responsibilities include validation, change control, CAPA, APR, compliance (supplie...
Jun 2011 — Jun 2013
Qa Manager
16640 Chesterfield Grove Rd SUITE 200, Chesterfield, MO 63005
May 2006 — Apr 2009
Monitoring Technician Ii
10255 west Higgins Rd SUITE 100, Rosemont, IL 60018
Feb 2000 — Sep 2002
Senior Airman, Cardiopulmonary Journeyman
Texas
Lackland AFB, Sheppard AFB, Kirkland AFB.
Jul 1995 — Jul 1999
Education
2014 — 2017
2002 — 2004
2000 — 2002
Occupations
Executive
Director
Leader
Doctor of Medicine
Operations Manager
Managers
Skills
Capa
Quality System
Validation
Change Control
Quality Assurance
Fda
Gmp
Six Sigma
Pharmaceutical Industry
21 Cfr Part 11
V&V
Sop
Regulatory Requirements
Technology Transfer
Quality Control
Quality Auditing
Gxp
Regulatory Affairs
Continuous Improvement
Manufacturing
Glp
Lims
Computer System Validation
Leadership
Medical Devices
Biopharmaceuticals
Supplier Quality
Design Control
Iso 13485
Staff Development
Corrective and Preventive Action
Project Delivery
Iso 14971
U.s. Food and Drug Administration
Verification and Validation
FAQs about Felix Martinson
What's the profession of Felix Martinson?
This professional's job is Director, Combination Products Program
What jobs is Felix a professional at?
Felix Martinson is proficient at Executive and Director jobs.
Where does Felix Martinson live?
They lives in Saint Louis, Missouri.
What is the professional's email?
The professional's email is fe**@pfizer.com and fe**@hotmail.com.
How many companies did Felix Martinson work at?
Felix Martinson worked at 12 jobs.
Where has Felix Martinson studied?
Felix studied at the Washington University In St. Louis from 2014 to 2017.
Are there any special industries, that Felix Martinson is connected to?
This professional works in Pharmaceuticals industry.
What are the skills of Felix Martinson?
This person has such skills as Capa, Quality System, Validation, Change Control, Quality Assurance, Fda, Gmp, Six Sigma, Pharmaceutical Industry, 21 Cfr Part 11, V&V, Sop, and Regulatory Requirements.