i-Pharm Consulting

Validation Officer

Location
Netherlands
Salary
Negotiable
Posted
27 Nov 2018
Closes
12 Dec 2018
Ref
CM-VAL-NL
Contract Type
Permanent
Validation Officer, Netherlands



Job Title: Validation Officer
Location: Netherlands
Benefits: Above market rate salary + fantastic benefits package



A position has become available in the Validation Team due to the expansion on my diagnostics services client’s state of the art site in the Netherlands. It will be the Validation Officer’s responsibility to ensure validation of the computerised systems in order to keep in line with company and industry standards, as well as maintain integrity of data for customers. They must be well-familiar with validation documentation, compliance and be able to overcome challenges. The ideal candidate must be a proactive team player who is target driven and produces work to a high standard.



Validation Responsibilities:

* Document and coordinate the validation activities and findings for a range of systems and equipment
* Prepare, draft, implement and archive validation and CSV documentation
* Execute and report validation protocols in line with Quality and Health & Safety
* Ensure GMP compliance in the validation activities
* Deal with unexpected problems efficiently and quickly
* Perform risk assessments and participate in audits



Job Requirements:

* MBO / HBO in biology, engineering, IT or similar
* Work experience in a pharmaceutical or biotechnology company
* Experience in ICT and computerised systems
* Knowledge of GAMP5, 21 CFR Part 11 or EU Annex 11
* Understanding of GLP compliance and GxP procedures
* Dutch and English fluency
* Skills – target driven, quality mindset, problem solver, multitasker, organisation and communication



About i-Pharm Consulting:
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

To apply:
If you would like to discuss this vacancy further, please call Charlotte Miles on +32 (0) 2 808 2403, or email cmiles@i-pharmconsulting.com. If this role is not suitable, Charlotte is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

Keywords:

Pharma / pharmaceutical / biotech / manufacturing / clinical / distribution / medical devices / Benelux / Netherlands / Belgium / Amsterdam / Eindhoven / the Hague / Maastricht / Rotterdam / Dutch / den Haag / Recruiter / recruitment / contract / permanent / career opportunities / QA / quality assurance / quality control / officer / manager / validation / audit / project manager / project management / research / GMP / GLP

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