Req #: 180004TV_en
Location: Thetford, ENG UK
Job Category: Quality
Date Posted: 3/14/2018 12:19:05 PM
Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anaesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
A Career That Matters
Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.
This role is for a Computerised Systems Validation Engineer within a team that design and perform validation activities associated with new installation projects and improvements to the existing manufacturing process, at the Thetford plant.
This role is responsible for authoring, executing and reporting computerised systems validation activities within the framework of cGMP and in compliance with Baxter Global QMS requirements. Within this role, the engineer will be required to manage multiple validation projects, liaising with the project team and all associated departments on site relating to the validation objects and work is completed in a timely manner.
Minimum degree level education preferably in engineering or alternatively in Pharmacy, Chemistry, Microbiology, or similar or equivalent industry experience.
Specific training and education in computerised systems validation and / or their implementation in the pharmaceutical industry is preferable.
Must be fully conversant and trained in EU GMP Annex 11 and GAMP 5
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, colour, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.