Quality Assurance Pharma

MANTU GROUP SA; Frosinone; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A multinational consulting firm in Frosinone is seeking a Quality Assurance Associate to support quality initiatives and manage supplier activities. The successful applicant will oversee compliance with GMP requirements, conduct supplier assessments, and handle documentation including CAPAs. A relevant scientific degree and proficiency in English are essential. This position offers a multicultural work environment and career growth opportunities.

Servizi

International and multicultural work environment

Clear career path with growth opportunities

Continuous training programs

Competenze

• Bachelor's degree in a relevant scientific field is essential.
• Must be proficient in English.
• Capable of managing GMP deviations and conducting investigations.
• Experience in coordinating root cause analysis and risk assessments.
• Ability to track and close CAPAs effectively.
• Familiarity with GMP compliance and support during audits.

Mansioni

• Maintain records related to suppliers and materials.
• Assist in supplier assessments and documentation.
• Manage GMP deviations while ensuring proper investigation.
• Monitor supplier performance and support change control processes.
• Collaborate on quality investigations and CAPA follow-up.

Conoscenze

Attention to detail

Organizational skills

Collaboration

Communication

Proficiency in English

Formazione

Scientific degree in Pharmaceutical Sciences, Biology, or Chemistry

Descrizione del lavoro

We are seeking a dedicated and detail-oriented Quality Assurance Associate to join our team in Frosinone. The successful candidate will play a crucial role in supporting the Supplier Quality organization by managing supplier-related activities and ensuring compliance with quality standards.

Your missions

Maintain and update records related to external suppliers, including information on materials, qualifications, and monitoring activities.

Assist in supplier assessments and manage supplier documentation, including:

• Specifications agreements
• Manage and oversee GMP deviations, including investigation and documentation

Follow-up on activities related to supplier performance

Support change control processes to ensure effective management of supplier changes.

Assist in the management and follow-up of activities related to EQ-SQ/Supplier investigations and Corrective and Preventive Actions (CAPA).

Collaborate on projects as part of a team.

Your profile

• Scientific degree in a relevant field (Pharmaceutical Sciences, Biology, Chemistry, or related area).
• Proficiency in English (mandatory).
• Manage and oversee GMP deviations, including investigation and documentation
• Coordinate and review root cause analysis and risk assessments
• Define, track, and close CAPAs, ensuring effectiveness and timely implementation
• Monitor deviation and CAPA trends to identify systemic issues
• Ensure compliance with GMP requirements and support audits and inspections
• Strong organizational skills and attention to detail.
• Ability to work collaboratively in a team environment.
• Excellent written and verbal communication skills.

What we offer

An international and multicultural work environment within a fast-growing consulting company.

A clear career path with personalized growth opportunities (both vertical and horizontal).

Continuous training and development programs through our internal Academy.

The opportunity to contribute to innovative projects with leading international clients in the Life Sciences sector.

At Amaris Consulting, we believe that diversity is a strength and we are proud to be an equal opportunities employer. We welcome applications from all backgrounds and are committed to fostering an inclusive environment where every voice is heard and valued.