QA Specialist - Life Science - Contract - Clonmel
Our partner in the Tipperary area develops and supplies active ingredients and final formulated products 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 worldwide, with primary markets in Europe, the USA, and Japan.
QA Specialist Responsibilities:
1. Provides knowledge and experience in Quality Systems and/or Operational Quality, including Quality Notifications, Investigations, LIR coaching, GCM coaching, environmental monitoring, sterility assurance, low bio-burden manufacturing, and customer complaint investigations.
2. Uses knowledge to improve Quality Systems, solve problems, drive continuous improvement, and execute tasks.
3. Contributes to compliance in project teams and leads small projects.
4. May coach and guide colleagues within the site.
5. Understands and applies regulatory and compliance requirements relevant to their role, staying current on upcoming regulatory changes.
6. Makes decisions within guidelines and policies, impacting priorities and time management to meet deadlines.
About you:
1. 1-5 years of experience in the pharmaceutical industry or a similar environment, including experience in a Quality function.
2. Demonstrated knowledge across more than one pharmaceutical and/or chemical manufacturing operation (e.g., Quality, Science).
3. Operational experience with at least 4 Quality Management Systems (QMSs).
If you are a good fit for a QA Specialist, get in touch with us today.
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