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About
Find out exactly what skills, experience, and qualifications you will need to succeed in this role before applying below.
This is a hybrid role requiring 3 days on-site.
Responsibilities include developing validation documentation in a pharmaceutical environment.
Ideal candidates have at least 5 years' experience and must possess strong knowledge of GMP and automation systems.
Full-time position with mid-senior level expectations. xcfaprz
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Remote working/work at home options are available for this role.
Languages
- English
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