Validation Engineer - New COVID Facility

INTRODUCTION

i-Pharm Consulting are partnered with a truly unique biotechnology development organisation with an outstanding reputation on the global market. They are looking to strengthen their validation team with a proven validation professional who is looking to take their career to the next level. The role will be based at their state-of-the art Hertfordshire facility.

TITLE

- Validation Engineer

JOB SUMMARY

- Truly unique biotechnology company with year-on-year growth
- State of the art GMP cleanroom facilities with challenging projects and role variance
- Opportunity to lead technical/corporate projects
- Opportunity to grow within the organisation
- Working at the forefront of the UK's cell and gene therapy market
- Close-knit cohesive team

LOCATION

- Essex, UK


RESPONSIBILITIES

- Ensuring the QMS is maintained in line with business distribution requirements for related regulatory standards
- Conducting validation activities to ensure compliance with full GxP systems
- Involvement with various departments departments for operational validation scopes (e.g. GAMP)
- Input to all stages of the validation lifecycle (IQ/OQ/PQ) requirements in support of smooth operation and business growth
- Deputise for the Validation Manager as and when required
- Active collaboration with management for continual quality performance improvement for the overall function

REQUIREMENTS

- A Level or above
- 3+ years' experience within a regulated GMP environment
- Demonstration of validation experience (equipment/process/cleaning/method/CSV/facilities etc.)
- Experience of QMS support (CAPAs, raising non-conformances, deviation assessment, risk analysis etc)
- Effective communication skills
- Ability to work alone or as part of a team


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, Validation and Bioinformatics.
www.i-pharmconsulting.com


TO APPLY

If you would like to discuss this vacancy further, please call Team Leader Dominic Williams on +44 (0)20 3873 7066, or email dwilliams@i-pharmconsulting.com. If this role is not suitable, Dominic is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

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