QA Specialist – Technical

Full Time Permanent

South Wales Jobs

QA Specialist – Technical

We are exclusively partnered with one of our most established clients and are now helping them hire for a new hire within the technical QA team as a result of internal promotion.

With the benefit of a global, established name, yet working on the specific site in South Wales within a growing and collaborative team, this opportunity gives you the chance to be a part of a rapidly growing business and to make a genuine contribution. Our client has gone from strength to strength in recent years and after expanding their current site, has further plans for headcount expansion across 2022 and beyond.

The position:

The successful individual will be part of a small team responsible for overseeing the approval, maintenance and review of technical documentation on a behalf of the QA function. This will focus on all documentation related to both of the clinical and commercial projects. This individual will also have involvement with external client meetings as well as participating in internal and regulatory body audits.

Experience required:

* Significant experience within GMP is essential (ideally pharmaceuticals but other GMP environments will be considered).

* Ideally, some previous experience within a direct QA capacity

* Background from analytical science (pharma) or pharmaceutical operations will be considered if the individual can demonstrate a good awareness of QA processes

* Strong communication skills and comfortable liaising with internal and external stakeholders

Key Words:

Pharmaceutical, pharma, QA, quality, technical, operations, analytical, QC, development, manufacturing, documentation, audit, validation, regulatory, notified, CAPA, change, control, systems, QMS, deviation, root, cause, investigation, batch, review, release

Harris Lord is acting as a Recruitment Agency in respect to this vacancy


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