QA Specialist job in Waterford, Éire

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First Name*

Last Name*

Email*

Phone Number*

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First Name*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: Ireland

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a QA Specialist to join a pharmaceutical organisation. This role is on a contract basis and is located in Waterford on a hybrid basis.

Responsibilities:

Collaborate with pertinent divisions/project teams to guarantee closure of quality actions/discoveries in a timely manner.
Partake in constant improvement initiatives.
Conduct evaluation of documentation, investigations, reports, highlighting and supporting the resolution of issues commensurate with the risk in a timely manner.
Serve as a quality main point of contact for projects offering leadership/feedback on quality concerns.
Offer QA assistance to new and ongoing projects.
Evaluate and approve of change controls, deviations, CAPA's, protocols reports, quality events and tasks.
Other duties may be assigned to this role.

Key Skills and Requirements:

Educated to a degree level in a science or similar field.
Familiarity within quality assurance/projects would be ideal.
Capable of offering quality knowledge and aid to the QA team and site teams.
Able to assist with the delivery of tasks in a highly regulated manufacturing setting.
Communication skills both verbally and in writing to a varied audience.
Expertise on needs for cGMP, US and EU regulatory needs.
Comprehension of pertinent quality and compliance guidelines.
Capable of handling projects/budget.
An efficient enabler.

If you are having difficulty in applying or if you have any questions, please contact Numhom Sudsok at +44 203 8718 093.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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