Consultant for this discipline
Gregory Sivo
Founder · Practising GMP quality professional
- · Founder, Truex Consultancy: GMP and GDP compliance
- · 10+ years in regulated pharmaceutical quality
- · Personally conducts every technical conversation
0 vacancies
GMP Auditing & Compliance jobs in Oss
GMP Auditing & Compliance jobs in Oss at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There are currently 0 open roles in Oss and the surrounding area. GMP Auditors, Supplier Quality Specialists, Compliance Managers and inspection-readiness leads for self-inspection, supplier audits and regulatory inspections. GMP jobs in Oss: a century of pharmaceutical manufacturing, Pivot Park's biotech cluster and some of the largest biologics and API sites in the Netherlands, with lower housing costs than the Randstad. Salaries for GMP Auditing & Compliance roles run from €62–92k gross per year across medior to senior profiles; interim day rates and regional differences are in our salary guide. Every vacancy states the client type, contract form, salary band and whether Dutch is required. Not seeing the right role? Register and we will call you when one opens; most GMP Auditing & Compliance roles in this market are never advertised.
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Register / upload CVFrequently asked questions
How much travel does a GMP Auditor role involve?
Supplier auditing means regular travel, often internationally; internal audit and compliance roles are mostly on site. We state the expected travel on every vacancy.
Do I need a certification to audit?
Not legally, but a recognised auditing qualification and documented lead-auditor experience are what most sites ask for. Experience hosting inspections weighs at least as much.
What is the difference between a GMP and a GDP audit?
GMP audits cover manufacturing and testing; GDP audits cover storage and distribution. Many auditors do both, and sites with their own distribution increasingly ask for both.
What is Pivot Park?
An open-innovation life-science campus in Oss with around 70 companies, biotech, CDMOs and analytical services, built around a large pharmaceutical manufacturing heritage.
Are there freelance validation projects in Oss?
Regularly. Biologics DSP and fill/finish expansions generate CQV projects of 6–18 months at €85–105 per hour.