QA Specialist - Life Science - Contract - Clonmel
Our Partner in Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at its manufacturing and R&D facilities. The plant, which has been operating in Clonmel for over 40 years, exports to over 25 countries around the world with primary markets being Europe, USA and Japan.
QA Specialist Responsibilities:
1. Provides to the site knowledge and experience in Quality Systems and/or Operational Quality, including the following i.e. Quality Notifications/ Investigations/LIR coaching; GCM coaching, environmental monitoring program, sterility assurance/low bio-burden manufacturing, customer complaint investigations etc.
2. Uses knowledge to improve Quality Systems, solve problems, provide continuous improvement and execute tasks.
3. Provides compliance contribution to project teams and leads small projects.
4. May coach and guide colleagues within the site.
5. Understands and applies regulatory / compliance requirements to their role together with remaining current on upcoming regulatory and compliance changes.
6. Makes decisions within guidelines and policies which impact own priorities and allocation of time to meet deadlines.
About you:
7. 1 - 5 years’ experience in the Pharmaceutical industry or a similar operating environment which includes experience in a Quality function.
8. Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation (i.e. Quality, science etc.)
9. Operational experience of at least 4 QMSs.
Are you a good fit for a QA Specialist? Get in touch with us today.
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