R&D Analytical Supervisor

ICAP Executive Search & Selection is one of the premium consultancies and part of ICAP People & Employment Solutions, the largest HR Services Provider in Greece and Cyprus. With more than 50 years of experience, we specialize in assessing and recruiting Senior to Middle Level Executives across all sectors.

ICAP Executive Search & Selection on behalf of its client, a well-established Pharmaceutical company with a strong foothold and dynamic growth in Greece, is looking for a talented R&D Analytical Supervisor, passionate about pharmaceutical research and development.

R&D Analytical Supervisor (Ref. 5414/RDA/ESS/GR)

Main Responsibilities:

• Develop analytical techniques for emerging finished products.
• Produce comprehensive technical documentation, including reports, protocols etc.
• Validate newly developed analytical methods for evolving finished products.
• Overview stability studies throughout the pharmaceutical development phase.
• Maintain meticulous records of analytical method validation processes.
• Offer technical assistance for analytical initiatives within pharmaceutical development.
• Aid in the seamless transfer of analytical methods for newly introduced products.
• Perform routine maintenance and troubleshoot issues related to HPLC and GC equipment/methods.
• Ensure adherence to cGMP, GLP, safety regulations, and SOPs within the laboratory.
• Uphold a high standard of record-keeping, ensuring accuracy and timeliness of data.
• Collaborate with cross-functional teams to provide analytical support for research projects and product development.
• Ensure compliance with regulatory requirements and industry standards in all analytical activities.
• Work closely with the Head of the department, stay informed about the latest developments in techniques and contribute to the continuous improvement of laboratory practices.

• Demonstrated expertise with 5-7 years in an Analytical Research and Development department.
• Bachelor’s degree in Chemistry, Pharmacy, or a related field; a Master’s degree is advantageous.
• Proficiency in the development and validation of common pharmaceutical analytical methods, including HPLC, GC, and UV-VIS.
• Advanced proficiency in MS Office, particularly Excel.
• Exceptional command of both written and spoken English.
• In-depth knowledge of global regulatory requirements.
• Effective communication and collaboration skills.
• Initiative and ownership.
• Robust problem-solving capabilities, coupled with the capacity to work autonomously.
• Proven project management skills emphasizing quality and adherence to timelines.