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Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Baxter Thetford has an opportunity for a Validation Engineers on an 24-month FTC basis. You will design and perform validation activities associated with new installation projects (CSV / Equipment / Facilities / Utilities / Systems), to the existing manufacturing process and manufacturing of Intravenous products at the Thetford plant. This role is Monday - Friday, 37.5 hours per week based on site in Thetford. Typical hours are 09:00-17:00 but there is flexibility on your start/finish time.

As a Validation Engineer onsite you will be developed into a primary contact and validation guide, responsible for authoring, driving and reporting validation activities within the framework. You will lead multiple validation projects, liaising with the project team and various departments relating to the validation ensuring work is completed in a timely manner.

You will be trained on the of Validation requirements for Equipment / Facilities / Utilities including associated control systems. In addition, you will gain the working knowledge in EU GMP Annex 11, 21 CFR Part 11, GAMP 5 and associated computerised system validation within the pharmaceutical environment.

You will receive an attractive salary and fantastic company benefits which are listed below.

25 days annual leave + bank holidays

Employee discount scheme

Blue light card

Progression opportunities

Substided canteen

Westfield healthcare

Up to 8% pension contribution

Employee assistance programme

Duties & responsibilities

Lead validation activities on specific projects including defining the validation requirements to ensure compliance with Annex 11, 15 and industrial guidance such as GAMP.

Ability to perform Risk Assessments, such as Failure Mode Effect Analysis (FMEA) for example, to critique a process or equipment and thereby define the level and scope of validation required.

Ability to write User Requirement Specifications, Design / Installation / Operational / Performance Qualification protocols and reports for validation and / or trial purposes.

Run validation project execution DQ/IQ/OQ/PQ in conjunction with relevant collaborators ensuring timelines are met and work achieved.

Proactively coordinate validation activities and act as a central point of contact for the project team for validation to ensure the projects are delivered on schedule.

Be involved in the Implementation of a risk-based approach to the validation of systems including computerised systems residing in Thetford.

Plan and prioritise their workload to ensure that agreed deadlines are met.  This includes coordinating and performing validation activities, tracking and reporting the progress of activities, anticipating and removing obstacles to progress.

Qualifications/experience required

Degree level education in Pharmacy, Chemistry, Biology, Microbiology, Engineering or similar

Minimum 2 years’ experience and a strong working knowledge of Qualification and Validation (for example, Equipment, Utilities, Facilities, Computer Systems and Cleaning).

Excellent communication skills

The ability to work as part of a multifunctional team but also independently

What happens next?

Baxter Talent Acquisition team will review your application and if your skills are a good fit, we will send you a hirevue assessment to complete online. This acts as a first stage interview and allows us to get to know you a little better. If successful you will then be invited on site for an interview and tour.

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Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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