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Pharmathen

Develops generic drugs and delivery technologies

QMS & Compliance Senior Officer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMunicipality of Pallini, GreeceNo salary listed

About the Job

Requirements

  • Educational background in Chemical Engineering, Chemistry, Biological Sciences, or Pharmaceutical Sciences.
  • 3–5 years of experience in Quality Management.
  • Excellent written and spoken English communication.
  • Broad knowledge and extensive experience with pharmaceutical quality systems.
  • Extensive knowledge of European Good Manufacturing Practices to ensure compliance with national and European standards and legislation.
  • Ability to prioritize tasks and meet deadlines.
  • Effective problem-solving ability.
  • Initiative and creativity.

Responsibilities

  • Participate in the preparation, authorship or review, and issuance of site standard operating procedures, technical documentation records, and other controlled documents within the company's Quality System.
  • Conduct regular audits and inspections to monitor compliance with Quality Management System principles and regulatory requirements, identify improvement areas, and ensure corrective actions are implemented.
  • Provide staff with training and guidance on Quality Management System procedures, compliance obligations, and quality assurance best practices.
  • Ensure that the Quality Management System meets International Standard ISO 9001 and European Union current Good Manufacturing Practices requirements.
  • Communicate with customers about quality queries related to facility activities.
  • Participate in multidisciplinary investigation teams.
  • Collaborate with cross-functional teams to align on quality and compliance objectives and foster a culture of quality across the organization.
  • Follow the company's Quality Policy and comply with current operational standards and legislative requirements.
  • Own document management, the training system, audit management including self-inspection, risk management, escalation processes, complaint management, corrective and preventive actions, other Quality Management System policies, regulatory compliance activities, and data integrity-related activities.
  • Actively participate in standard operating procedure and master record preparation and review; deviation handling; change management; out-of-specification and out-of-trend investigations; utilities and environmental monitoring; statistical evaluations; annual product quality reviews; process and cleaning validations; aseptic process simulations; key performance indicator monitoring; stability oversight; transfer, engineering, and computer systems validation projects; and data integrity campaigns.

About the Company

Pharmathen

Develops generic drugs and delivery technologies

Pharmathen develops generic medicines and advanced drug-delivery technologies from its Greece-based manufacturing sites, exporting to branded pharmaceutical companies and patients worldwide. Its products include long-acting injectables, sustained-release formulations, and ophthalmic drugs, built on a strategy of Life Cycle Management and new technology platforms. The company operates with full vertical integration, handling research, development, manufacturing, and export, under facilities approved by the US FDA and EU. This enables it to deliver high-quality generic solutions and optimized dosage forms at scale. Pharmathen differentiates itself through a focused emphasis on drug-delivery platforms, continuous pipeline development, and end-to-end control over development and manufacturing. Its goal is to provide high-quality, affordable medicines while expanding its capabilities in innovative generic products and advanced delivery technologies for global markets.

Company size
501-1,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Athens, Greece
Founded
1969

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