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R&D Scientific Affairs Expert (Thessaloniki)

Demo S.A.

Thessaloniki, Central Macedonia, Greece permanent

Posted: March 13, 2026

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Quick Summary

Design and develop generic drug products in accordance with GMP requirements and company policies in a fast-paced environment.

Job Description

At DEMO SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a high – skilled R&D Scientific Affairs Expert. The purpose of the role is the design and development of generic drug products in accordance with GMP requirements and company policies. This position is based in Thessaloniki.

Responsibilities

• Lead the development and optimization of analytical methods for new raw materials and pharmaceutical products, as well as improvements of methods for already approved products.
• Draft validation and verification protocols for analytical methods in collaboration with Laboratory Supervisors and review the corresponding study reports.
• Prepare specification sheets for new products in collaboration with the CMC/R&D Manager.
• Evaluate laboratory analysis results and coordinate, together with Laboratory Managers, the repetition of analyses when required.
• Contribute to the design of studies addressing questions from regulatory authorities and clients.
• Ensure the smooth, efficient, uninterrupted, and safe operation of the Physicochemical Laboratory, Pharmaceutical Development Laboratory, and Microbiological Laboratory in compliance with Good Laboratory Practice (GLP).
• Ensure the timely execution of departmental activities, including development, optimization, and validation of analytical methods, scientific literature research, and preparation of technical reports.
• Communicate and collaborate with internal and external stakeholders to resolve scientific and technical issues within the department.


Requirements:
• Bachelor’s degree in Chemistry, Pharmacy, or a related field, followed by postgraduate studies (MSc or PhD) in a relevant discipline.
• Minimum 5 years of experience in Analytical Development.
• Hands-on experience in method development and validation using common pharmaceutical analytical techniques such as HPLC, GC, UV, LC/MS, and GC/MS.
• Experience with statistical software.
• Fluency in Greek and English.
• Strong computer skills.
• Strong problem-solving ability and capability to work independently.
• Project management skills with focus on quality, timelines, and study deliverables.
• Excellent verbal and written communication skills.


Benefits:
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.

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