Galenica is seeking a highly motivated Quality Control Analyst to join our dynamic laboratory team.

Main responsibilities of the role include:

•  Analytical Testing : conduct routine physicochemical testing of raw materials and finished pharmaceutical products to guarantee compliance with established regulatory guidelines and cGMP/GLP and daily schedule.
• Perform Quality Control activities according to instructions, procedures and protocols in compliance with the GMP principles
• Record, process and review analytical data, following strictly data integrity principles ALCOA+
• Support investigations for out-of-specification (OOS) results, out-of-trend (OOT) data, deviations, and CAPA (Corrective and Preventive Actions) 

Required skills:

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a closely related scientific discipline.
• At least 2-4 years of experience working in a pharmaceutical or related industry as a laboratory analyst
• Strong knowledge of analytical techniques and instrumentation such as HPLC, GC etc.
• Familiarity with Industry standards and regulations
• Attention to detail, the ability to work in a team and excellent analytical skills
• Fluency in English and fully computer literate
• Military obligations fulfilled for male applicants
• Excellent communication and organizational skills