RAW MATERIALS SCIENTIST

Sector: Pharmaceutical and biopharmaceutical

Pharmaprogress is a reliable Contract Research Organization part of the Kymos Group, a fast growing company with a strong commitment to quality and a dedication to innovation. Our customers have access to a wide range of GMP/GLP-certified and GCP-compliant services and obtain a tailor-made, personalized, genuinely flexible service into a unique selection of services for innovative small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA (anti-drug antibodies), ADC (antibody-drug conjugates), hormones, enzymes and nucleic acids.

We are looking for a Scientist in the area of testing and certification of raw materials to ensure the correct development of assigned analytical projects.

The responsibilities of the position include:

• Design, supervise, and execute quality control testing of raw materials.
• Manage assigned projects, keeping deadlines and establishing direct communication with clients.
• Write technical documents associated with studies (protocols, reports, standard procedures, certificates of analysis).
• Direct and supervise the experimental work of technical staff.
• Perform the work in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

Requirements

• Bachelor’s degree in chemical or Biochemical Sciences.
• Knowledge of HPLC and GC techniques, with an understanding of analytical development departments.
• Skilled in physical/chemical properties determination.
• Familiar with the use of Pharmacopoeias.
• Experience in managing technical documents associated with studies (standard procedures, certificates of analysis, deviations, OOSs, CAPAs, etc.).
• Experience working in GLP and GMP environments is required.
• Experience in similar roles in the pharmaceutical industry.
• Detail-oriented and able to achieve objectives.