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Qualified Person - Pharmaceutical GMP OSD Oncology

Job description

Are you a QP Qualified under an EU regulation, but are not on a license and/or never practiced, but are looking to take up a QP post? Depending on the past experience I may have a role for you within a leading pharmaceutical manufacturer in Dublin.

Or maybe you are an experienced QP (junior or senior) looking to make a move?

Contact

If you are interested in this job apply below.

I also have more senior or indeed junior roles within Engineering, QC, QA, QP, Validation, CQV, PM and other areas of pharmaceutical, medical device, and biologics companies. Nationwide!

Send me an email or simply your CV to schedule a confidential chat (014744692) - to andrius "at" sigmar.ie

Job Responsibilities
-Management of batch disposition and material status control.
-Review and record of essential documentation and SOPs.
-Provide support to QA team.
-Support both, the internal and external audits.
-Ensure compliance according to cGMP practices.
-Ensure compliance with specific regulatory frameworks.

Essential Job Requirements
-Primary Scientific degree.
-Education requirements to satisfy EU directive 2001/83/EC of a Qualified Person.
-Experience in QA
-GMP knowledge as per FDA and EMEA regulation for oral solid dosage pharmaceutical manufacturing.

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