Rene Boes
Auditor | Audit en Risk Management | at Royal Avebe | Tynaarlo, Drenthe, Netherlands
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Rene Boes currently serves as an Auditor within the Audit en Risk Management team at Royal Avebe, where he plays a pivotal role in safeguarding the company's compliance with rigorous quality and food safety standards. Leveraging over three decades of extensive experience in the Pharma and Food industries, Rene brings a wealth of expertise in conducting comprehensive internal and external audits, with a particular focus on ISO 9001, ISO 22000, and ISO 14001 standards. His deep understanding of GMP, GCP, GLP, and GxP regulations ensures that Royal Avebe maintains the highest levels of product safety, quality, and regulatory adherence.
In his current role, Rene is instrumental in leading risk-based audits that identify potential vulnerabilities within the supply chain, production processes, and vendor relationships. His proficiency in computerized systems auditing, including compliance with 21 CFR Part 11, enables the company to optimize digital quality management systems and ensure data integrity. Rene actively contributes to continuous improvement initiatives by analyzing audit findings, implementing CAPA plans, and fostering a culture of compliance and quality excellence across the organization.
Furthermore, Rene’s expertise extends to training and mentoring staff on regulatory requirements and best practices in quality management. His leadership in activating and empowering teams aligns with his skills in volunteering management and employee activation, ensuring that quality assurance remains a shared responsibility. With his comprehensive knowledge of food safety, risk management, and regulatory frameworks, Rene Boes continues to be a vital asset in maintaining Royal Avebe’s reputation for safety, quality, and sustainable innovation.
Auditor | Audit en Risk Management | at Royal Avebe in September 2024 to Present
Senior Auditor, Quality and Compliance at ICON plc in July 2021 to September 2024
Senior Auditor, Global Quality / Lead Auditor GLP, G(C)LP, GMP at Pharmaceutical Research Associates, Inc. in April 2017 to July 2021
Quality Assurance Officer at Pharmaceutical Research Associates, Inc. in July 2005 to April 2017
Quality Assurance Auditor at Pharma Bio-Research Group B.V. in January 2001 to July 2005
Technician Laboratory for Chromatography/Robotics at Pharma Bio-Research Group B.V. in December 1993 to January 2001
Quality Systems Associate at Abbott in January 1995 to December 1995
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Lloyd’s Register Quality Assurance, Lead Auditor, July 2026
Business Administration (Higher Vocational Education), Post Bachelor, July 2026
Business Administration (Higher Vocational Education), July 2026
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Auditing
Vrijwillligers aansturen
Activeren van medewerkers
Quality System
GxP
Clinical Research
GLP
Validation
CTMS
Quality Management
LIMS
21 CFR Part 11
Process Improvement
Quality Assurance
Clinical Development
GMP
Pharmaceutical Industry
FDA
GCP
Good Laboratory Practice (GLP)
U.S. Food and Drug Administration (FDA)
Laboratory Information Management System (LIMS)
Good Clinical Practice (GCP)
U.S. Title 21 CFR Part 11 Regulation
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Discover more about Royal AvebeWhat is Rene Boes email address?
Email Rene Boes at [email protected], [email protected] and [email protected]. This email is the most updated Rene Boes's email found in 2026.
How to contact Rene Boes?
To contact Rene Boes send an email to [email protected], [email protected] or [email protected]. (updated on March 06, 2025)
What company does Rene Boes work for?
Rene Boes works for Royal Avebe
What is Rene Boes's role at Royal Avebe?
Rene Boes is Auditor | Audit en Risk Management |
What is Rene Boes's Phone Number?
Rene Boes's phone (**) *** *** 926
What industry does Rene Boes work in?
Rene Boes works in the Pharmaceuticals industry.
Rene Boes Email Addresses
Rene Boes Phone Numbers
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