Senior QA Specialist - Ireland - Rapidly Growing

Senior QA Specialist - Ireland - Rapidly Growing

My client is a Biotech company, experiencing rapid expansion, which plan on being the biggest site in Europe. They are now looking for an experienced QA Professional to join their team on the west cost of Ireland. This is an opportunity to join their select team that is already leading the way in the Pharmaceutical/Biotech industry.

Salary: €50,000 - €60,000
Job type: Permanent
Location: Limerick (offer relocation package)

This position offers the exciting chance to join an established company while they're in a great financial situation and looking to expand further as soon as possible. As my client has one of the fastest growing sites in Europe, this is an amazing opportunity to grow with the company and within it, giving you the chance to progress as fast as your abilities let you.

Requirements:
* Understanding of aseptic filling and/or packaging operations is preferred.
* Requires good written, verbal and interpersonal communication skills and the ability to effectively interact cross functionally. And cross-organisationally.
* Ability to prioritise, manage multiple tasks, and meet deadlines
* Ability to travel up to 25% of time.
* Requires BS/BA in scientific discipline or related field and minimum 2 year's relevant Biologic experience.

Responsibilities:
* Represent Quality Assurance both internal and External with Partners and Contract Manufacturers in support of complex Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution
* Train and/or mentor junior employees, including providing insights and education on processes and procedures;
* Provides consultation or advice in alignment with QA policies; and develop an understanding of external partner and manufacturers site procedures.
* Perform activities associated with reading product records for disposition (e.g. manufacturing record review, receipt, inspection, document review, shipping, etc.). Activities may be on site at a partner or contract manufacturer or at a desk
* Review, edit, or approve controlled documents
* Review and approval of investigations associated with raw materials, product, laboratory, facilities, and materials.