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QC Compliance Specialist
- Contract
- Good Manufacturing Practice (GMP)
- Ireland
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting for a QC Compliance Specialist to join a pharmaceutical organisation. This role is on a contract basis and is located in Waterford.
Responsibilities:
- You will raise, handle and close all quality system procedures which involves allocated change controls, deviations, CAPAs, ILIs & QEs.
- You will drive all quality metrics for the division forward evaluate quality metrics to guarantee no over-dues.
- Responsible for process efficiency and simplification as well as partaking in continuous improvement initiative.
- Guarantee efficient arrange and assist for both internal and external audits for the division.
- Conduct crucial/constructive evaluate of processes and practices.
- Uphold training in crucial test actions as necessary in the lab.
- Recognise and lead projects to make step change improvements to the division's quality.
- Partake in continuous improvement initiatives utilising lean strategies where suitable.
- Mediate with the quality assurance representative to assist and improve on RFT in the area and always audit ready.
- Any other assigned duties.
Key Skills and Requirements:
- Educated to a degree level in a scientific/engineering field or similar.
- Expertise on cGMP and GDP, as well as quality systems all within a regulated setting.
- A high attention to detail.
- Interpersonal abilities.
- Knowledge of continuous improvement techniques.
If you are having difficulty in applying or if you have any questions, please contact Will Hitchcock at w.hitchcok@proclinical.com.
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.
#QACompliance
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