GMP Quality Assurance Specialist

Philogen S.p.A.; Siena; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading biotechnology company located in Siena seeks a GMP Quality Assurance Specialist to manage key quality policies, oversee documentation, and ensure compliance with GMP regulations. Candidates should have a strong scientific background and prior experience in quality assurance. This full-time role offers a contract and salary based on experience.

Competenze

• A good scientific background (ideally in Biology, Biotechnology, etc.)
• Previous experience in Quality Assurance (at least three years)
• Comprehensive knowledge of GMP and other regulations.

Mansioni

• Writing, reviewing and approving documents (SOPs, PQRs, IMPDs, validations, etc.)
• Revision of production and quality control batch records
• Managing GMP QA operations and documentation systems

Conoscenze

Attention to detail

Flexibility in tasks

Interpersonal skills

Ability to work independently

Formazione

Degree in Biology or Biotechnology

Descrizione del lavoro

Direct message the job poster from Philogen S.p.A.

GMP Quality Assurance Specialist

Philogen S.p.A. is looking for a GMP Quality Assurance Specialist who will report to the GMP Quality Assurance Manager and who will give his/her contribution to quality policies in support of Philogen’s Quality System.

In particular the successful candidate will be responsible for:

• writing, reviewing and approving documents (SOPs, PQRs, IMPDs, validations, research reports, etc.);
• revision of production and quality control batch records;
• managing GMP QA operations, change control, deviation and documentation systems;
• identifying and recommending future improvements;
• implementing action plans;
• developing quality strategies and priorities and translating them into short and long-term objectives;
• interacting with other members of the company and clinical center staff.

The ideal candidate should have:

• A good scientific background (ideally in Biology, Biotechnology, etc.)
• Previous experience in Quality Assurance (at least three years);
• Comprehensive knowledge of GMP and other regulations with a good understanding of global quality standards relating to product development, submission and clinical experimentation;
• A high level of English language, both written and spoken;
• A high level of attention to detail and with the ability to prioritize working tasks;
• A strong flexibility in changing tasks and priorities;
• The ability to work independently as well as coordinate members of his/her team;
• Excellent interpersonal skills and ability to work in teams.

We offer:

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

Job location:

Siena

We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Pharmaceutical Manufacturing