Description
Validation EngineerExciting opportunity available for and experienced Validation Engineer to work on new production line project for a world leading pharmaceutical company based in the South East. Our client is looking for a Validation Engineer to help close out this large scale project onsite.
Key Responsibilities:
- Generation and execution of validation documentation of equipment in a sterile environment.
- To ensure that all documentation is prepared, authorised and completed in a timely manner.
- To communicate effectively with others on site.
- To maintain an understanding of current international regulatory requirements, ISO, and GMP.
- To ensure compliance with the sections and site procedures.
- Comply with GMP requirements and company rules, policies and procedures.
Qualifications/Experience:
- Degree or recognised experience equivalent
- In-depth knowledge and understanding of cGMP
- Sterile Manufacturing experience
- Vial line experience beneficial
- Experience with Sterilisation tunnels, VHP, Autoclaves, Disinfectants and Inspection Machinery.
- Writing and execution of validation documentation.
- Dynamic, self-motivated, pro-active approach to taking on challenging assignments.
- Creativity, judgement and analytical thinking.
- Ability to work with critical timelines.
This is an urgent requirement, please apply immediately for consideration.