RAW MATERIALS SCIENTIST

Kymos Group; Ancona; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a dedicated Scientist to join their team in the testing and certification of raw materials. This role involves designing and supervising quality control testing, managing projects while ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The ideal candidate will have a Bachelor’s degree in chemical or biochemical sciences and a strong understanding of HPLC and GC techniques. This position offers a unique opportunity to contribute to important analytical projects in a collaborative environment focused on excellence and innovation in the pharmaceutical industry.

Competenze

• Bachelor’s degree in chemical or Biochemical Sciences is essential.
• Experience in GLP and GMP environments is required.

Mansioni

• Design and execute quality control testing of raw materials.
• Write technical documents associated with studies and manage projects.

Conoscenze

Knowledge of HPLC

Knowledge of GC techniques

Teamwork skills

Detail-oriented

Formazione

Bachelor’s degree in chemical or Biochemical Sciences

Strumenti

Pharmacopoeias

Descrizione del lavoro

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).

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.
• Teamwork skills.
• Detail-oriented and able to achieve objectives.