Quality Assurance Pharma

Amaris Consulting; Frosinone; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A fast-growing consulting company in Frosinone is seeking a Quality Assurance Associate to manage supplier-related activities and ensure compliance with quality standards. The ideal candidate will have a scientific degree and proficiency in English, along with strong organizational skills and attention to detail. This role offers opportunities for career growth and development within an international and multicultural environment, contributing to innovative projects in the Life Sciences sector.

Servizi

Clear career path

Continuous training and development programs

Multicultural work environment

Competenze

• Proficiency in English is mandatory.
• Strong collaborative skills in a team environment.
• Ability to monitor deviation and CAPA trends.

Mansioni

• Maintain and update records related to external suppliers.
• Assist in supplier assessments and manage supplier documentation.
• Collaborate on projects as part of a team.

Conoscenze

Attention to detail

Excellent written and verbal communication skills

Organizational skills

Formazione

Scientific degree in Pharmaceutical Sciences/Biology/Chemistry

Descrizione del lavoro

Job Description

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.