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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:
5
Posted:
14.06.2025
Expiry Date:
29.07.2025
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 relevant legislation.
* Implement and maintain the company’s documentation system according to cGMP.
* Oversee production, warehousing, quality assurance, and quality control activities to ensure compliance with cGMP.
* Update the quality system with new guidelines and EU directives.
* Draft and maintain high-level documents such as the Site Master File, Validation Master Plan, and SOP list.
* Participate in management reviews and advocate continual improvement.
* Ensure effective communication and escalation of quality issues.
* Define responsibilities related to Pharmacovigilance and perform internal audits in this area.
* Conduct Product Quality Reviews.
* Monitor QA key indicators, deviations, change controls, and approve corrective actions.
* Supervise GMP/QC-GLP assessments in production and warehouse areas.
* Train personnel on GMP/QC-GLP concepts and review training needs.
* Participate in internal audits and prepare relevant documentation.
* Qualify and audit suppliers and contract laboratories, and prepare audit reports.
* Participate in audits by authorities and customers.
* Manage corrective action plans and related documentation post-audit.
* Ensure qualification of GMP-related vendors.
Candidate Profile
* At least 10 years of experience in a similar pharmaceutical QA role.
* Extensive knowledge of quality guidelines (ICH, WHO, etc.).
* Strong understanding of EU-cGMP Quality Systems.
* Fluent in English, 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 contacted.
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