Shift Lab Supervisor

Novartis Italia; Torre Annunziata; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Torre Annunziata seeks a Shift Lab Supervisor to manage quality aspects in the laboratory. You will oversee production, ensure compliance with cGMP standards, and support team activities. The ideal candidate has a scientific degree, relevant GMP experience, and fluent Italian and English skills. This role offers opportunities for professional growth and collaboration in a dynamic environment.

Competenze

• Previous experience in a similar role within a GMP laboratory.
• Proven people management skills.
• Knowledge of Quality tools.

Mansioni

• Manage Quality aspects and projects within the laboratory.
• Ensure compliance with cGMP and data integrity.
• Oversee production and testing activities.

Conoscenze

People management

Knowledge of IT applications

Fluency in Italian

Fluency in English

Formazione

Scientific degree

Descrizione del lavoro

Summary

The Shift Lab Supervisor manages Quality aspects and projects within area of responsibility.

Ensures, within the assigned laboratory in Quality Control, the execution of planned analytical activities by coordinating the use of available resources and facilitating operational teams, in compliance with laws and company policies and procedures regarding HSE (Health, Safety, Environment), cGMP (current Good Manufacturing Practices), the Quality System, safeguarding company assets, and the Code of Conduct.

About The Role

Major accountabilities

• Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance.
• Define, in collaboration with your manager, the planning (weekly/monthly) and scheduling (daily) of laboratory activities.
• Proactively support the team in analytical activities, continuous improvement, and "right first time" (Lean Lab).
• Perform review of analytical documents and analytical approval of batches, verifying that analytical activities are executed and documented according to the current Testing Monographs and that analytical tests are performed on equipment properly qualified and calibrated according to their respective programs.
• Ensure proper management of reagents, materials, and standards (adequate stock and storage per current procedures), coordinating material procurement requests, monitoring costs, and proposing any containment actions.
• Perform, if necessary and according to prescribed methods, chemical, physico-chemical, microbiological, classical and/or instrumental analyses on substances examined within the assigned laboratory, across multiple products and using a wide range of complex and diverse equipment, in full compliance with HSE and cGMP standards.
• Ensure correct entry of analytical data under your responsibility into the quality control management system (LIMS – Laboratory Information Management System).
• Support, including through external suppliers, IQ/OQ/PQ activities for laboratory equipment (Installation/Operational/Performance Qualification).
• Staff training.
• Support exception investigations and OpEx improvement projects.

Essential Requirements

• Scientific degree.
• Previous experience in a similar role within a GMP laboratory.
• Proven people management skills.
• Knowledge of IT Applications & Quality tools.
• Fluent in Italian and English.

Why Novartis

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

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Benefits and Rewards

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