Validation Consultant
- Randstad
- 4000.00 - 6000.00
- 32-40 uren
- 1 year, contract to hire with client
- Bachelor degree
Opdrachtgever
Our client is an international consultancy supporting leading pharmaceutical organisations with complex validation and compliance challenges.
Opdrachtgever
Our client is an international consultancy supporting leading pharmaceutical organisations with complex validation and compliance challenges. Consultants work on projects involving equipment, process and system validation within GMP environments, combining technical expertise with a practical, hands-on consulting approach.
functie Vereisten
- A Bachelor's or Master's degree in Engineering, Life Sciences, Pharmaceutical Sciences or a related field
- Experience with validation within the pharmaceutical or Life Sciences industry
- Good understanding of GMP and validation principles
- Experience with IQ/OQ/PQ and validation documentation
- Strong analytical and problem-solving skills
- A structured, accurate and hands-on approach
- Strong communication skills and professional proficiency in English
- Dutch is an advantage
Wat krijg je?
- Pension entitlement (15.9% employer contribution, 7.5% employee contribution)
- Collective WGA / WIA insurance
- NBBU collective labour agreement through equal remuneration
- 25 holidays days
- 8% holiday allowance
- 100% payment in case of illness in the first year
- Travel allowance per kilometer or through public transport
Werkzaamheden
Are you passionate about ensuring that pharmaceutical processes, equipment and systems consistently meet the highest quality standards? As a Validation Consultant, you will support leading pharmaceutical organisations with validation activities within GMP-regulated environments.Your role:
You will work on a variety of validation projects, supporting clients from validation strategy through execution and documentation. Your responsibilities may include:
- Performing equipment, process and system validation
- Preparing and executing IQ, OQ and PQ protocols
- Developing and reviewing validation plans, protocols and reports
- Supporting Computer System Validation (CSV) activities
- Performing risk assessments and identifying validation requirements
- Managing validation-related deviations and change controls
- Ensuring validation activities comply with GMP requirements
- Supporting continuous improvement of validation processes and documentation
