Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 140+ countries worldwide. Originally founded in 1980, it went through various development stages. Today Remedica is specialising in the development, production, and sale of high-quality, safe, and efficacious pharmaceutical products for human use. Our pharmaceutical range consists of a product portfolio of more than 300 generic, branded generic, and over-the-counter (OTC).

Over the last few years, Remedica went through a massive transformational program from a locally recognized reputable company to a global player, respected by its distributors, partners, and clients. The investments into the factories, R&D equipment, new facilities, implementation of best-in-class software, and people development are the baselines for Remedica's success in the future.

We are looking for:

A Production Quality Officer  to support the implementation of quality system changes and compliance initiatives within the Production department. Working closely with both QA and Production teams, this role ensures that new or revised procedures, tools, and quality standards are embedded effectively into daily operational routines.

As a Production Quality Officer you will:

• Act as the production point of contact for quality changes initiated by QA.
• Ensured SOPs, policies, and procedural changes are understood and implemented correctly in the production environment.
• Assist in rollout of initiatives such as deviation/CAPA process changes, documentation practices, right-first-time programs, etc.
• Coordinate and support training for operations teams on new quality-related procedures.
• Monitor adherence to new practices and escalate issues or resistance to supervisors/managers.
• Participate in internal audits or self-inspections to verify the effectiveness of change implementation.
• Support data gathering and reporting on key quality metrics within operations (deviations frequency, RTFT, CAPA on time etc.).
• Maintain accurate records of implementation progress and follow-up actions.
• Identify practical challenges during implementation of quality initiatives and propose improvements or mitigation plans.
• Support improvement workshops (e.g., Gemba walks, 5 Whys, root cause analysis sessions etc.) in coordination with Quality and Production leaders.
• Facilitate strong communication between QA and Production teams during transformation activities.
• Provide feedback from operators and technicians to QA to ensure solutions are practical and sustainable.

What you will bring:

• Degree or diploma in Pharmacy, Biotechnology, Chemistry, Engineering, or related discipline.
• Relevant experience in GMP operations may be accepted as an alternative to formal education.
• 2–5 years of experience in pharmaceutical operations or quality roles (Production, QA, Compliance, or similar).
• Familiarity with cGMP principles, deviation/CAPA systems, and basic change control processes.
• Experience supporting audits, shop floor training, or procedural rollouts is a plus.

Why Join Remedica? At Remedica, we offer a competitive compensation package, including 14 salaries, a provident fund, and a range of additional benefits to support your personal and professional growth. Join our team and be part of a company that values innovation, teamwork, and continuous improvement.