Job Description
Job Title:  QC Supervisor
Job Location (Short):  Cyprus, Limassol
Req ID:  859

Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 160+ 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.

 
Job Description: 

 

We are looking for:

Highly skilled and experienced QC Supervisor to supervise QC personnel and coordinate the assigned products/materials’ analysis, safeguarding that the required tasks are completed in accordance with the relevant specifications.


As a QC Supervisor you will:

  • Coordinating the tests and completion of the required documentation according to written procedures and specifications.

  • Approving the audit trail procedures to ensure data integrity.

  • Reviewing laboratory documents (such as reports, methods and analytical protocols).

  • Providing guidance and supervision to Senior Analysts, Analysts, Junior Analysts and Assistants.

  • Evaluating the performance of team personnel, identifying training needs, reviewing the time and attendance of team personnel and processing leaves applications.

  • Communicating updates as regards the status of analysis to Planners, Unit Heads and QC Management..

  • Ensuring that tasks, analysis and projects are completed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and the current Good Manufacturing Practices (cGMP).

  • Carry out any other duties as assigned by the immediate supervisor.

 

What you will bring:

 

  • Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline

  • Minimum 5 years of experience in a Quality Control laboratory within the pharmaceutical or related industry

  • Strong knowledge of cGMP, cGLP, and relevant regulatory requirements for pharmaceutical manufacturing and testing.

  • Proven experience in coordinating laboratory activities, including the testing of raw materials, intermediates, and finished products.

  • Experience with reviewing and approving laboratory documentation, including analytical protocols, methods, and audit trails.

  • Demonstrated ability to lead, supervise, and evaluate performance of laboratory personnel.

  • Strong analytical and problem-solving skills with attention to detail and data integrity.

  • Excellent organizational and time-management abilities with a track record of meeting deadlines and managing multiple priorities.

  • Effective communication skills, both verbal and written, with the ability to collaborate with cross-functional teams.

  • Proficiency in laboratory systems and equipment; familiarity with LIMS or similar quality management systems is an advantage.

  • Fluency in English (written and spoken) is essential.

 

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.
Apply now