Shift Lab Supervisor

Novartis; Torre Annunziata; In loco; EUR 40.000 - 65.000; Tempo pieno

Descrizione del lavoro

A global healthcare company in Torre Annunziata is seeking a Shift Lab Supervisor to manage Quality aspects in their laboratory. The role involves ensuring compliance with cGMP regulations, overseeing production and testing activities, and facilitating continuous improvement in analytical activities. The ideal candidate will have a scientific degree, previous experience in a GMP lab, strong people management skills, and fluency in Italian and English. This full-time position offers an opportunity to make significant impacts in a dynamic organization.

Competenze

• 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.

Mansioni

• Manage Quality aspects and projects within the assigned laboratory.
• Ensure compliance with cGxP, including data integrity and eCompliance.
• Review analytical documents and approve batches.
• Ensure proper management of reagents, materials, and standards.
• Perform chemical, physico-chemical, microbiological analyses on substances.

Conoscenze

Continued Learning

Dealing With Ambiguity

Decision Making Skills

Gxp Industry Standards

Laboratory Equipment

Laboratory Excellence

Quality Control (QC) Testing

Quality Control Sampling

Self‑Awareness

Technological Expertise

Total Quality Management

Formazione

Scientific degree

Descrizione del lavoro

Job Description 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.

Major accountabilities

• Oversight of all production and testing activities ensuring compliance with cGxP, including 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 approval of batches, verifying that analytical activities are executed and documented according to 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 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.

Skills Desired

• Continued Learning
• Dealing With Ambiguity
• Decision Making Skills
• Gxp Industry Standards
• Laboratory Equipment
• Laboratory ExcellenceQuality Control (QC) Testing
• Quality Control Sampling
• Self‑Awareness
• Technological Expertise
• Total Quality Management

Required Experience

• Manager

Employment Type

Full‑Time

Experience

years

Vacancy

1