Quality Specialist

Responsibilities

• Support the implementation and ongoing maintenance of the company’s Quality Management System (QMS), ensuring accurate and timely handling of records such as deviations, change controls, and complaints.
• Identify compliance gaps and recommend appropriate corrective and preventive actions (CAPAs).
• Ensure CAPAs are properly documented, monitored, and completed within agreed timelines.
• Monitor, analyse, and report on quality metrics and key performance indicators.
• Review and approve batch documentation to enable timely release of products to the market.
• Prepare Annual Product Quality Reviews in line with internal procedures and schedules.
• Coordinate stability programs for locally managed products.
• Assist with internal self-inspection activities and audits.
• Contribute to management reviews of quality systems and processes.

Qualifications

• Bachelor’s degree in a Life Sciences field (such as Biology, Chemistry, or Pharmacy).
• Ideally 1–2 years of experience in a pharmaceutical quality-related role.
• Strong organisational skills with the ability to manage tasks through to completion.
• Excellent written and verbal communication skills.
• High level of accuracy and attention to detail.
• Proficiency in Microsoft Office applications (e.g. Excel, Word, Outlook).

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

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