Quality Assurance Engineer

For almost six decades, Pharmathen has remained committed to its vision of improving patients’ lives through innovation and expanding access to complex pharmaceutical therapies.

Today, Pharmathen's capabilities extend across a broad range of specialized dosage forms, including sustained-release products, long-acting injectables, and oral solid dosage forms, while its portfolio includes more than 100 commercial products available internationally through a strong network of partners.

These activities are supported by a robust Research & Development and Manufacturing ecosystem, with three facilities in Greece.

The driving force behind Pharmathen is its people. With more than 1,600 employees representing 27 nationalities, the company fosters a multicultural workplace where women account for 53% of the workforce and 40% of the Senior Leadership Team.

Grounded in its shared values of integrity, quality, innovation, leadership and performance, and guided by strong business ethics and a commitment to its vision, Pharmathen remains dedicated to its founding mission: improving patients' lives.

Pharmathen offers a great opportunity for career development and is seeking to recruit a Quality Assurance Senior Engineer to join our Quality Assurance team at our Pallini premises.

As a Quality Assurance Senior Engineer, the ideal candidate will ensure compliance of equipment, processes and plant areas to EU cGMPs and ISO requirements, be responsible for organizing new areas and equipment projects as per quality demands and for customer communication regarding engineering topics and interdepartmental communication, and play a key role in all calibration/qualification activities.

Requirements

More particularly:

What you’ll do:

• Responsible for issuance of TDR and SOPs relevant to operation, maintenance, cleaning and validation/qualification activities of areas and equipment
• Ensure compliance with legislation requirements regarding change controls, deviations, risk management related to equipment and areas
• Ensure compliance to the Quality Management System according to ISO 9001:2015 and EU cGMPs
• Responsible for the preparation and control of the controlled layouts of the plant and the warehouses
• Responsible for issuance, conducting and monitoring of protocols, that will be used for validation and/or qualification of equipment, warehouse and production areas
• Keep a key role in project plans regarding new areas and equipment and have the main role for internal and subcontractors communication
• Design, develop, execute, monitor and control the internal Validation/Qualification procedures of the equipment/premises, utilities and production areas and evaluate findings of measurements and studies, according to legislation and company’s standards