Quality assurance specialist tempo determinato

JR Italy; Varese; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical sector is seeking a Quality Assurance Specialist for their Saronno site. The role involves managing QA activities, ensuring compliance with GMP regulations, and maintaining regulatory documentation. Candidates should have a degree in scientific disciplines and knowledge of GMP guidelines.

Servizi

Daily lunch voucher of €8.00

Competenze

• Degree in Pharmacy, Chemistry, Biology, Engineering, or Biotechnology required.
• Knowledge of GMP regulations and ability to manage technical documentation.

Mansioni

• Manage QA activities and collaborate on technical documentation verification.
• Assist in drafting protocols and participate in internal inspections.

Conoscenze

Knowledge of GMP regulations

Technical documentation management

Formazione

Degree in scientific disciplines

Descrizione del lavoro

Job Title: Quality Assurance Specialist

Company: Gi Group

Location: Saronno (VA)

Job Category: Other

EU work permit required: Yes

Job Description:

Grafton LifeScience, a division of Gi Group dedicated to Clinical Research, Regulatory, Operations, Sales & Marketing in the Pharmaceutical and Medical sectors, is seeking a Quality Assurance Specialist for their Saronno site. This role reports directly to the Quality Assurance Manager and involves managing QA activities.

Main Responsibilities:

1. Collaborate with the team to verify and manage technical documentation related to quality of machines, software, and environments involved in production, storage, and packaging of active substances and materials.
2. Assist in drafting protocols and validation reports for processes and cleaning.
3. Participate in internal inspections to verify GMP compliance, prepare reports, and ensure corrective actions are implemented.
4. Manage client audits and prepare/manage CAPA documentation.
5. Maintain regulatory documentation such as Site Master File and Validation Master Plan.

Requirements:

• Degree in scientific disciplines (Pharmacy, Chemistry, Biology, Engineering, Biotechnology).
• Knowledge of GMP regulations and related guidelines.
• Ability to understand, draft, and manage technical documentation.

Contract type: Fixed-term (6 months), with a chemical-pharmaceutical CBA, daily lunch voucher of €8.00.

Gi Group is part of Gi Group Holding, Italy's leading multinational employment agency, authorized by the Ministry of Labour and Social Policies.

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