QA Officer - Pharmaceutical
|Job Title:||QA Officer - Pharmaceutical|
|Contact Name:||Adrienn Prezenszki|
|Job Published:||August 16, 2019 14:28|
Whilst we will consider science graduates with less experience, it will be a strong advantage if you have some experience from either a QA team or a similar department where you need strong attention to detail, excellent communication and the ability to scrutinise documents and data.
Full details will be provided on application. The company offers a competitive salary, based on experience, and you will work in a supportive and friendly and fast-paced environment where achievement and ambition are appreciated, recognised and rewarded.
You will join a busy QA department that supports all company activities with close links to Manufacturing, Packaging, Validation, QC and Product Development, Sales & Marketing and Regulatory Affairs. This role will focus on various aspects of the Quality Management System. Using your skills to the full, you will undertake document control and systems administration, process customer complaints (using Trackwise), write detailed and clear reports, maintain systems compliance, analyse data, and undertake a range of other responsibilities relating to Quality within a highly regulated Pharmaceutical production facility.
This is a broad, challenging role that requires meticulous attention to detail, strong communication skills and the ability to multitask. Full details will be provided on application.
A pioneering Europe-based Pharmaceutical organisation who manufacture specialised treatments for people suffering from life-threatening diseases. Their products are fascinating, complex and ever-changing. You will be based in a pleasant setting in Worthing which has an excellent reputation for providing career development opportunities, challenging and engaging work and a vibrant working environment.
We are inviting candidates with a scientific, technical or manufacturing background, with experience in report writing, good attention to detail when looking at data and trends, and experience in filing and administrative duties. Strong report writing skills would be a big advantage. Experience gained in Pharmaceutical Manufacturing testing or Quality Assurance environment paired with knowledge of GxP and GMP will be looked upon favorably. You will demonstrate the ability to multitask, use basic statistical tools and methods plus have proven abilities in Word, Excel and/or Access to process and display data graphically. Experience of using Trackwise would be advantageous to your application. In addition, you will need a strong and enthusiastic work ethic, excellent communication skills and attention to detail and enjoy a closely-knit team environment.
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