GMP Auditor (two positions), Espoo / Turku / Stock

Description of unit:

The Quality System Unit maintains and develops the current quality system and monitors the regulatory environment. Our main target is to improve the robust Orion interpretation of policies in the ever-changing GMP field. Another significant target is to clarify and simplify our quality system.

Main responsibilities of the Quality System Unit are:
- technical QA operations
- computerized QA operations
- GxP Training
- SOP-system
- Supplier audits
- Internal Audits
- Inspections conducted by authorities
- Quality Agreements
- Regulatory Intelligence

Description of position:

We are looking for two experienced professionals to join our Quality System team as a GMP-Auditor.

In the first position your main goal is to quarantee Orion's suppliers' compliance levels by conducting GMP-audits of contract manufacturers. The second position is GMP Auditor for materials (API, excipient, packaging materials).

Our suppliers are located around the world and produce final dosage forms for Orion (e.g. sterile and non-sterile, human medicines, veterinary products, CE-marked products).

You may also be responsible for some defined projects related to Quality Management and Vendor Management.

Positions can be located in Espoo or Turku, Finland or in Stockholm, Sweden.

Requirements:

We require:
- Pharmaceutical or scientific education
- Several years of experience in pharmaceutical industry
- Experience of GxP-requirements
- Excellent negotiation and co-operation skills
- Fluent English
- Readiness to travel abroad

We offer:

We offer you a challenging field of work and interesting tasks in Quality Management. You will have the opportunity to get a broad picture of Orion's extensive supplier network while working for a trusted, well-established, innovative pharma company.

Apply here: https://express.candarine.com/campaign/url/forward/5f1b80123ef1