Supervisor, Manufacturing Monza

Supervisor, Manufacturing
Monza
Lombardia, Monza

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion.

Our Mission is to enable our customers to make the world healthier, cleaner and safer.

Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or developing and manufacturing life-changing therapies, we are here to support them.

Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

The PDS business unit, part of DPD Monza site is looking for a Supervisor for manufacturing.

The resource will be rin charge of the manufacturing activities of a department producing 24/7 sterile products in vials (liquid and lyo form) or pre-filled syringes on two production lines fully following new Annex 1 requirements.

Isolator barrier with automatic VHP decontamination cycle, multi format lines, automatic system for lyophilized loading and unloading: the equipment of the PDS department represents the state of the art in terms of Sterile Production Technology.

Customer portfolio balanced between new pharma companies approaching clinical phase I/II/III study and big Pharma approaching new technology (e. g. . mRNA products) makes PDS production environment dynamic, sophisticated and aiming to continuous improvement.

The Manufacturing Supervisor, reporting to the Manufacturing Manager, will be supported by the team of Manufacturing Team Leader/Lead and will collaborate daily with Quality, MSAT, Logistic Engineering Dept.

and all other site functions to achieve customer happiness and deliver products to patients in need.

A growing unit where the Manufacturing Supervisor contribution is essential in terms of processes and flow optimization.

Main tasks will be:

- Guarantee the achievement of the production objectives of the assigned department in terms of quantity, times, costs, quality, through the direction, coordination, training and control of the dependent structure, the contribution to the creation of instructions regarding production operations, verifying compliance with the master batch record, coordination with other departments, in compliance with the budget, customer needs, GMP, company quality procedures and standards, safety and environmental impact regulations.

Production

- Ensure the production - also guaranteeing the slots dedicated to validation/revalidation and preventive maintenance activities - of the drugs requested by the customer, through the direction, coordination and control of the assigned dependent structure, the contribution to the creation of instructions regarding the operations production, any support in the event of anomalies with respect to production standards, the coordination of the activities of the assigned department with the other departments of the Production function, the order of the needed consumables, in compliance with the budget, the customer's needs in terms of quantity, times, quality, GMP, procedures and company quality standards.

Quality

- Ensure an adequate level of the warehouse of the assigned department, through the definition of the minimum orders and the direction, coordination and control of the Department Supervisor in the order of the consumables for production, as codified by the pharmaceutical formulations, in case is not leading the Warehouse function, in compliance with the assigned budget.

Cost check - Support the Production Manager in controlling costs and verifying their trend, through the correct association of costs with the order and the verification of orders for consumables, in compliance with production objectives.

Maintenance

- Support the Technical Services function in the maintenance of production plants, through the direction, coordination and control of the dependent structure in verifying the state of efficiency of the assigned department, of the equipment, the timely reporting of anomalies, support in the definition of actions suitable for solving production problems (system failures), in compliance with quality standards and quantitative production requirements.

Thermo Fisher Scientific is an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, creed, religion, colour, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Join us and be part of our amazing mission to enable our customer to make the world healthier, cleaner and safer!