Our client is expanding their team in Malta and is seeking a Senior QA Specialist. Reporting directly to the Quality Manager, your responsibilities will include:
- Manage and oversee the Quality Management System (QMS) by developing procedures, compiling quality metrics, and supporting data-driven decisions.
- Provide quality oversight for operational activities, including SOPs, and ensure compliance with GMP requirements.
- Support the CMC function by addressing GMP and QMS-related queries, tracking project progress, and ensuring timely follow-up on CAPAs, deviations, and change control actions.
- Maintain stability programs, monitor release data, review manufacturing records, and oversee the issuing and evaluation of Product Quality Reviews.
- Handle investigations of manufacturing deviations and complaints, track CAPAs, and utilise quality tools to conduct root cause analyses and drive continuous improvement.
- Monitor and manage risks, change controls, and ensure effective communication with third-party suppliers.
- Participate in internal and external audits, self-inspections, and regulatory inspections to maintain compliance and readiness.
- Contribute to overall QMS operations and support other reasonable activities as needed.
Working Hours: Monday - Friday: 08:30 - 17:30
Requirements
- Minimum 3 years of experience working in a similar role within the pharmaceutical industry.
- Experience in utilising of quality System processes (such as, Audit, Deviations, CAPA, Risk assessments & Change Control)
- Fluency in English, both written and verbal.
- Experience of authoring SOPs, reports, protocols and other GxP documents.
- Ability to work in a fast-paced environment and under pressure.
- Must be already based in Malta.
Benefits
- Hybrid work model
- 10% performance bonus
- Health and life insurance
- Mobile phone and mobile allowance
- Free parking
- Wellbeing program
Job Reference: YB224
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