Description
Our global pharmaceutical client is undergoing a brownfield construction to bring a new product onsite. The equipment for this new product is now onsite needs to be taken from commissioning to full working status.They are looking for someone to:
-Commission new equipment
-Write validation documentation from scratch (SAT, IQ/OQ)
-Execute the validation documentation.
Requirements
-Hands on experience of execution of validation of equipment in a pharmaceutical company.
-Experience of writing validation documents is essential.
-Solid experience of commissioning of new equipment in a pharmaceutical environment.
-Strong stakeholder communication skills with suppliers and internal stakeholders.
-Strong organisation and project delivery skills.
-Ability to work as part of a team and offer support where required.
It is a busy buzzing atmosphere onsite, a company that has received excellent feedback for customer satisfaction