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Open nowPosted 37 days ago

QC Deputy Manager

Workable (global search)108,016 open roles

Where
Kifisia, Attica, Greece
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Your applicationOpen nowQC Deputy ManagerWorkable (global search) · Kifisia, Attica, Greece

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7.9% of postings close within 7 days. Measured by our own scanner across the market. Workable (global search) postings stay open a median of 7 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 7.9%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted 37 days ago

Workable (global search) median: 7 days open

The posting

InterMed, is a leading Pharmaceutical Company with 26 years of experience in the production and distribution of pharmaceutical products. It continues to grow its portfolio and the markets where it operates daily.

We invest in modern production facilities, advanced technologies & highly qualified people sharing the same values as we. InterMed has been declared Top Employer in Greece for 2023, 2024, 2025 & 2026 by the Top Employer Institute. Our Compass is #TELEIA

  • Teamwork
  • Ethos
  • Learning
  • Excellence
  • Innovation
  • Accountability

We are looking for a self-motivated and experienced QC Deputy Manager to join our company at the Quality Control Department.

Key Responsibilities:

  • Supports the QC Manager in the effective operation and management of the Quality Control Department.
  • Supervises and coordinates daily Quality Control activities, ensuring timely and accurate execution of all laboratory operations.
  • Ensures compliance of Quality Control activities with GMP, regulatory requirements, approved procedures, specifications and company quality standards.
  • Coordinates and monitors the testing and release of raw materials, packaging materials, bulk and finished products, as well as stability samples, where applicable.
  • Reviews and approves analytical results, laboratory documentation, specifications, analytical methods and relevant Quality Control records.
  • Ensures the proper execution, review and documentation of laboratory investigations, OOS/OOT results, deviations and CAPAs.
  • Supports the implementation, validation and maintenance of analytical methods and laboratory equipment.
  • Ensures that laboratory equipment is properly maintained, calibrated and qualified according to applicable procedures.
  • Participates in the preparation, review and approval of Quality Control procedures, work instructions, protocols and reports.
  • Ensures the appropriate documentation, traceability and integrity of Quality Control data in accordance with Data Integrity principles.
  • Collaborates closely with Production, Quality Assurance, R&D, Regulatory Affairs and other relevant departments to support business and quality objectives.
  • Supports internal and external audits and regulatory inspections, ensuring the timely preparation and provision of required documentation and information.
  • Contributes to the identification and implementation of continuous improvement initiatives within the Quality Control Department.
  • Supports the QC Manager in resource planning, workload allocation and prioritization of departmental activities.
  • Participates in the training, development and performance evaluation of QC personnel.
  • Acts as Deputy for the QC Manager when required, ensuring continuity and effective operation of the department.

Requirements

  • Degree in Chemistry, Pharmacy, Chemical Engineering or a related scientific discipline.
  • 3–5 years of experience in a similar position within the pharmaceutical industry.
  • Strong knowledge of GMP and relevant pharmaceutical quality standards and regulations.
  • Experience in Quality Control laboratory operations, analytical testing and laboratory investigations.
  • Knowledge of OOS/OOT investigations, deviations, CAPA and change control processes.
  • Experience with analytical techniques such as HPLC, GC, UV-Vis, and other relevant laboratory methodologies.
  • Excellent knowledge of the English language.
  • Excellent computer skills (MS Office, Word, Excel, PowerPoint).
  • Knowledge of ERP systems, especially SAP, will be considered an advantage.
  • Excellent organizational, leadership, communication and problem-solving skills.
  • Ability to work effectively in a team-oriented and fast-paced pharmaceutical environment.
  • Strong attention to detail and commitment to quality and compliance.
  • Fulfilled military obligations (for male candidates).

Our vision is to improve people's lives...

That is why we are committed to serve medical science with passion, creativity and ethos, having human life as our top priority.

InterMed is an equal opportunity employer. We celebrate diversity and we are committed to provide a workplace that fosters creativity, growth, and inclusion.

This position offers an exciting opportunity to join the Quality Control Department at a key position, supporting the effective management of laboratory operations and ensuring the highest standards of quality, compliance and scientific excellence. The QC Deputy Manager will work closely with cross-functional teams, contribute to continuous improvement initiatives, develop people and play an important role in maintaining the company's commitment to pharmaceutical quality and patient safety.

Apply today to become part of our transformative journey in the pharmaceutical industry!

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