Validation Engineer

VALIDATION ENGINEER

Exciting 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.