Quality Assurance Pharma

Amaris Consulting

Latina

In loco

EUR 30.000 - 40.000

Tempo pieno

14 giorni+

Generatore di candidature

Fatti notare per questo impiego — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Robust training system

Vibrant workplace culture

Commitment to CSR

Descrizione del lavoro

An innovative consulting firm based in Latina, Italy, is seeking a Quality Assurance Specialist to ensure compliance with GMP and regulatory standards in the pharmaceutical field. This entry-level role involves document review, audits preparation, and supporting quality processes across projects. Candidates should have a Master's degree and a minimum of 6 months of relevant experience, along with fluency in Italian and English.

Competenze

Experience with Quality Assurance in the pharmaceutical industry (6 months minimum).
Fluent in Italian and English.
Attention to detail and ability to maintain high-quality standards.

Mansioni

Ensure compliance of pharmaceutical products with GMP and regulatory standards.
Perform document review and approval.
Support audits and regulatory inspections.

Conoscenze

Quality Assurance experience

GMP guidelines knowledge

Analytical skills

Organizational skills

Communication skills

Formazione

Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field

Descrizione del lavoro

Who are we?

Join our team and start a new adventure in an international and dynamic environment where you will be able to fulfil your career expectations in a fast-growing organization.

Being a consultant at Amaris Consulting means positioning yourself as a technical and functional expert in the pharmaceutical field, but above all being an ambassador of our organization to clients thanks to:

Your interpersonal skills and ability to listen in order to build a strong relationship of trust with our clients and fully understand their challenges and issues.
Your curiosity and eagerness to learn as we support over 1000 clients from all sectors worldwide.

Your missions

Ensure compliance of pharmaceutical products with GMP and regulatory standards.
Perform document review and approval (batch records, SOPs, quality manuals).
Conduct deviation analysis, CAPA implementation and monitoring.
Support audits and regulatory inspections by preparing documentation and answering queries.
Collaborate with production, R&D and supply chain teams to guarantee quality across processes.
Perform risk assessments and contribute to continuous improvement projects.
Provide training to colleagues on quality procedures and regulatory updates.
Prepare and present reports on quality indicators and project progress.

Your profile

Experience with Quality Assurance in the pharmaceutical industry (6 months minimum).
Knowledge of GMP guidelines and pharmaceutical regulatory standards.
Experience with deviation management and CAPA processes.
Academic background: Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field.
Fluent Italian and English.
You have strong organizational and analytical skills with attention to detail.
You are able to adapt quickly, work in a team and maintain high-quality standards.

What we offer

An international community bringing together 110+ different nationalities.
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities.
A robust training system with our internal Academy and 250+ available modules.
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.).
Strong commitments to CSR notably through participation in our WeCare Together program.

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability or other characteristics.

Seniority level