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Quality Assurance Manager, Nicosia, Sicily
Client:
GRS Recruitment
Location:
Nicosia, Sicily
Job Category:
Other
EU work permit required:
Yes
Job Reference:
5753a8c35ead
Job Views:
2
Posted:
06.05.2025
Expiry Date:
20.06.2025
Job Description:
A leading pharmaceutical company with global activities is working in partnership with GRS Recruitment to hire a Quality Assurance Manager to join their Nicosia based team. The successful candidate must have extensive working experience in a similar role within the pharmaceutical industry. If you are looking for the next step in your career, GRS looks forward to receiving your CV for this Nicosia-based Quality Assurance Manager role.
MAIN DUTIES AND RESPONSIBILITIES

Ensure the company’s Quality system is in line with current cGMP requirements and with any other relevant legislation.
Make sure that the company’s documentation system is correctly implemented and in line with current cGMP.
Ensure that the company’s production, warehousing, quality assurance and quality control activities are in line with current cGMP.
Keep the company’s quality system up to date by implementing any new guidelines or other legal requirements emanating from the E.U. Directives.
Draft and keep up to date high level documents such as the company’s Site Master File, Validation Master Plan, and the SOP list.
Participate in management reviews of process performance, product quality, and the quality management system, advocating continual improvement.
Ensure effective communication and escalation processes to raise quality issues to management.
Define responsibilities regarding Pharmacovigilance activities and perform periodic internal audits of the Pharmacovigilance department.
Ensure Product Quality Reviews are conducted.
Control and evaluate QA key indicators such as complaints, recalls, maintenance, calibration, and performance checks; monitor deviations; supervise change controls; approve corrective actions, changes, and master documents.
Supervise GMP/QC-GLP assessments in QC/Production/Warehouse areas for quality deficiencies.
Train personnel on GMP/QC-GLP concepts, including induction, initial, and periodic training with evaluations.
Participate in annual self-inspections and prepare reports and follow-up CAPAs.
Qualify, audit, and review local material suppliers and contract laboratories, and prepare audit reports with CAPA follow-ups.
Participate in audits by authorities and customers.
Manage corrective action plans post-audit and ensure close-outs are completed.
Monitor vendor qualification processes for GMP-related vendors.

CANDIDATE PROFILE

At least 10 years of experience in a similar pharmaceutical role.
Extensive knowledge of quality guidelines (ICH, WHO, etc.).
Strong understanding of EU-cGMP Quality System.
Fluent in English, both written and verbal.
Qualified Person registration in Cyprus or another EU country is an advantage.

COMPANY BENEFITS

13th salary
Provident fund
Flexible Working Hours

Due to high application volume, only shortlisted candidates will be responded to.
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