Job Description
Job Title:  QA Shopfloor Oversight Associate
Job Location (Short):  Cyprus, Limassol
Req ID:  1078

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.

 

Job Description: 

 

We are looking for:

A QA Shopfloor Oversight Associate to maintain a high-visibility Quality Assurance presence on the shopfloor, ensuring real-time compliance with Good Manufacturing Practices (GMP) and data integrity standards within a pharmaceutical manufacturing environment.

 

As a QA Shopfloor Oversight Associate you will:

  • Maintain a continuous and visible presence within manufacturing and packaging areas.
  • Spend the majority of working hours on the shopfloor rather than in office-based activities.
  • Observe production activities in real time to ensure compliance with GMP.
  • Engage with production personnel to promote quality awareness and compliance.

Rotational Oversight Across Production Areas

  • Rotate regularly between different production suites (e.g., every 1–2 days).
  • Ensure QA oversight across all manufacturing stages, including dispensing, granulation, compression, coating, and packaging.
  • Monitor consistency of compliance practices across departments.

Real-Time GMP Compliance Monitoring

    • Perform on-the-floor QA oversight of:
      • Line clearance activities
      • Batch manufacturing and packaging operations
      • Adherence to approved SOPs and GMP requirements
  • Identify, document, and escalate deviations or non-compliance.
  • Support immediate corrective actions in collaboration with production and QA teams.

    Data Integrity Oversight (ALCOA+)

    • Monitor documentation practices within batch records and logbooks.
    • Ensure compliance with ALCOA+ principles:
      • Attributable
      • Legible
      • Contemporaneous
      • Original
      • Accurate
    • Identify data integrity risks and ensure timely correction and escalation.

    Collaborative Shopfloor Support

    • Work closely with production teams to support compliant execution of manufacturing activities.
    • Provide guidance on GMP and documentation practices where required.
    • Maintain QA independence while fostering a collaborative working environment.

    Periodic QA Observation Reporting

    Prepare structured daily reports including:

    a. Scope of Activities

    • Areas visited
    • Personnel engaged
    • Products and batch numbers observed
    • Manufacturing steps reviewed

    b. Observations

    • GMP compliance observations
    • Data integrity findings
    • Deviations or potential risks identified

    c. Actions Taken

    • Immediate corrections implemented
    • Escalations to QA management

    d. Inspection Readiness

    • Ensure reports are detailed, clear, and suitable for Health Authority inspections (e.g., FDA, EMA).

    Continuous Improvement & Audit Readiness

    • Identify recurring issues and support root cause investigations.
    • Contribute to process improvements and strengthening of GMP practices.
    • Support maintaining a constant state of audit readiness across manufacturing operations.

 

What you will bring:

  • Bachelor’s degree in Pharmacy, Chemistry, Biology or related Life Sciences field.
  • Recent graduate or up to 1–2 years of experience in a GMP-regulated pharmaceutical manufacturing environment is preferred. 
  • Familiarity with shopfloor operations and QA processes is an advantage.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint)
  • English: fluent (written and spoken)
  • Greek: fluent (written and spoken) is an advantage

 

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.