QA Operations Scientist

Location: Limassol, Cyprus (On-Site)

Relocation Support Available

Advance Your Career in Pharmaceutical Quality

Are you an experienced Quality professional looking to make a real impact within a leading international pharmaceutical manufacturer?

At Remedica Ltd, we're seeking QA Operations Scientists to join our Quality Assurance team in Limassol . This is an exciting opportunity to play a key role in maintaining GMP compliance, supporting operational excellence, and ensuring the highest standards of quality, safety, and efficacy across our pharmaceutical products.

Working at the heart of our manufacturing operations, you'll gain broad exposure to quality systems, investigations, audits, risk management, and continuous improvement initiatives while collaborating with colleagues across the business to drive a culture of quality.

What You'll Be Doing

As a QA Operations Scientist, you'll play a vital role in maintaining and improving our Quality Management System and ensuring operational readiness across the site. Responsibilities include:

• Own GMP documentation, including SOPs, protocols, reports, and quality records.
• Lead investigations into deviations, OOS results, and quality events, driving timely resolution.
• Manage Change Controls and CAPAs, ensuring effective implementation and compliance.
• Support audits, inspections, and site inspection readiness activities.
• Conduct quality risk assessments and identify opportunities to strengthen compliance.
• Investigate customer complaints, temperature excursions, and product quality issues.
• Analyse quality metrics and trends to drive continuous improvement.
• Provide QA support to manufacturing operations through on-floor GMP oversight.
• Contribute to APQRs, quality reviews, and cross-functional quality initiatives.
• Mentor and support colleagues on GMP requirements, quality systems, and best practices.
• Champion a culture of quality, compliance, and operational excellence across the site.

What We're Looking For

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering, or a related scientific discipline.
• 2-3 years' experience within Pharmaceutical Quality Assurance, Quality Control, or GMP Manufacturing.
• Strong understanding of GMP requirements, quality systems, and regulatory compliance.
• Experience investigating deviations, CAPAs, change controls, or related quality processes.
• Excellent analytical and problem-solving skills.
• Strong communication and stakeholder management capabilities.
• High attention to detail and a passion for quality.
• Excellent English language skills; Greek would be advantageous.
• Experience working with electronic Quality Management Systems (eQMS) is beneficial.

This role is based fully on-site in Limassol, Cyprus, and we welcome applications from both local and EU candidates. For the right individual, we are happy to provide relocation support to help make the move as seamless as possible.

Ready to Join Us?

If you're passionate about quality, thrive in a GMP-regulated environment, and want to be part of a company that's making a difference in global healthcare, we'd love to hear from you.