GMP PRODUCTION SUPERVISOR

Philogen S.p.A. is looking for a young candidate with a brilliant academic background, preferably with experience in the pharmaceutical field, for a growth position in the company’s Production Department. He/she will work directly alongside the Department Manager, to take on increasing responsibilities over time.

The successful candidate will be responsible for:

• Supervising department activities in terms of efficiency and training;
• Ensuring department GMP documentation is drafted and updated;
• Ensures compliance with GMP and HSE Instructions during the course of the department’s activities by verifying the proper execution of GMP Instructions;
  Supporting the management of investigations, change requests and corrective, preventive or implementation actions for aspects pertaining to the production department;
• Reports to the Production Manager on the efficiency status of departments, equipment rooms and their maintenance and qualification;
• Participating in activity coordination meetings;
• Collaborating with QA to ensure Data Integrity;
• Managing warehouse requests and the progress of processing steps on the plant management system (ERP);
• Preparing the production activity plan for Management approval;
• Reviews, in the first instance, production documentation to ensure compliance with cGMP and departmental SOPs;
• Supporting the selection of suppliers of raw materials/materials and services for the Production department and drafts the URS.

The ideal candidate should have:

• A MSc/PhD in chemistry, pharmaceutical chemistry, biochemistry, molecular biology, or similar field.
• Excellent knowledge of the UNICORN platform for managing AKTA chromatography systems;
• Excellent knowledge of tangential filtration processes;
• Very good knowledge of GMP;
• Good knowledge of automated stirred-tank fermentation systems (i.e. Sartorius Biostat platform);
• Fast learning ability in the operation of complex automated systems.
  Will be considered a Plus:
• At least 5 years of experience supervising a production team working in the GMP area;
• A Good knowledge of English language.

We Offer:

A contract and salary proportional to the experience (seniority) of the successful candidate.

Job location:

Sovicille (SI)