Kees Ensing
Consultant at Kees Ensing Advies | Greater Groningen Area
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Kees Ensing is a highly experienced and versatile consultant specializing in quality assurance, compliance, and process optimization within the life sciences and healthcare sectors. Currently serving as a QC Manager at PolyVation in Groningen, Kees leverages his extensive expertise to oversee quality control operations, ensuring that innovative biotechnological products meet stringent industry standards. His role involves designing and implementing robust quality management systems (QMS), streamlining product development workflows, and fostering continuous improvement initiatives that enhance product safety and efficacy.
Throughout his career, Kees has demonstrated a strong capability in managing complex projects across pharmaceutical, medical device, and biotech industries. His previous positions, including QA Manager/QP at CIBG and Radiation Safety Officer at AAA Novartis, highlight his proficiency in regulatory compliance, GxP standards, and risk management. Kees’s experience in interim management and change management enables him to lead cross-functional teams through organizational transformations and process optimizations effectively.
At Kees Ensing Advies, his independent consultancy, he has successfully guided clients through the design, implementation, and validation of quality management systems, ensuring compliance with international regulations such as GMP, GCP, and ISO standards. His expertise extends to clinical trials, drug discovery, and medical devices, where he applies his deep understanding of pharmaceutics and healthcare regulations to improve product quality and operational efficiency. Kees’s comprehensive skill set, combined with his strategic approach to quality assurance and process improvement, makes him a trusted partner for organizations seeking to enhance their compliance posture and operational excellence in the highly regulated life sciences industry.
Consultant at Kees Ensing Advies in January 2003 to Present
QC Manager at PolyVation in November 2024 to December 2024
QA Manager/QP at CIBG in September 2023 to June 2024
Radiation Safety Officer at AAA Novartis in November 2022 to December 2022
Manager QA & Compliance/QP at Basic Pharma in May 2022 to August 2022
Person in Plant at Athersys in May 2021 to August 2021
QA Manager at Eurofins in December 2020 to March 2021
Director Commercial Quality Benelux/Nordic at Teva Pharmaceuticals in June 2020 to August 2020
QA/QC consultant at OQSIE at Sanofi in April 2020 to June 2020
QMS project leader at Comecer in June 2019 to September 2019
Head of Regulatory Affairs at Curium Pharma in September 2018 to December 2018
Quality Manager at Sanofi in January 2018 to July 2018
Consultant Quality Assurance at Arvato in September 2017 to October 2017
Senior QA at Patheon in January 2017 to March 2017
QA Operations Manager at Ajinomoto OmniChem in July 2016 to November 2016
Manager Quality Assurance & Compliance at Basic Pharma Group in January 2016 to May 2016
Senior QA at Sandoz BV in September 2015 to December 2015
Senior QA at RIVM National Institute for Public Health and the Environment in November 2014 to May 2015
Senior Quality Manager European Distribution Centre at Janssen, Pharmaceutical Companies of Johnson and Johnson in April 2014 to July 2014
Legacy review specialist (Global Remediation Quality Project) at Synthes in September 2013 to March 2014
Manager Quality Healthcare Division at Rexam in February 2013 to July 2013
Vennoot at MOM2006 in March 2006 to October 2012
Managing director at Merska in January 2000 to December 2003
Marketing Director at MIP Technologies in January 1999 to January 2002
Associate Professor Bioanalysis and Toxicology at University of Groningen in January 1990 to January 2000
Director of scientific affairs at Analytisch Biochemisch Laboratorium in January 1987 to January 1990
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University of Groningen, Ph.D., July 1982 to July 1984
Leiden University, M.Sc., July 1976 to July 1981
RSG Professor Zeeman
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Pharmaceutical Industry
Validation
Quality Management
Quality Assurance
GMP
Regulatory Affairs
Pharmaceutics
Change Management
Management
Quality System
Healthcare
GxP
Clinical Trials
Drug Discovery
Medical Devices
Life Sciences
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What is Kees Ensing email address?
Email Kees Ensing at [email protected], [email protected] and [email protected]. This email is the most updated Kees Ensing's email found in 2026.
What is Kees Ensing phone number?
Kees Ensing phone number is +31621822795.
How to contact Kees Ensing?
To contact Kees Ensing send an email to [email protected], [email protected] or [email protected]. If you want to call Kees Ensing try calling on +31621822795. (updated on March 23, 2025)
What company does Kees Ensing work for?
Kees Ensing works for Kees Ensing Advies
What is Kees Ensing's role at Kees Ensing Advies?
Kees Ensing is Consultant
What industry does Kees Ensing work in?
Kees Ensing works in the Pharmaceuticals industry.
Kees Ensing Email Addresses
Kees Ensing Phone Numbers
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