PQA Support

Boehringer Ingelheim; Fornovo San Giovanni; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

Una compagnia farmaceutica internazionale ricerca un supporto PQA per il suo stabilimento a Fornovo San Giovanni. Il candidato selezionato sarà responsabile delle attività di investigazione e gestione della qualità, collaborando su progetti di miglioramento e partecipando a audit. Si richiede un anno di esperienza e laurea in discipline scientifiche, con buone conoscenze di GMP e fluenza in italiano e inglese.

Servizi

Accesso gratuito alla mensa aziendale

Programmi di sviluppo professionale

Benefici per il benessere fisico, finanziario, sociale e mentale

Competenze

• Un anno di esperienza in un ruolo QA simile.
• Fluenza in italiano e buone capacità in inglese (livello B2).
• Conoscenza delle normative GMP.

Mansioni

• Gestione delle attività di indagine relative a non conformità e reclami.
• Collaborazione alla validazione dei processi di produzione.
• Partecipazione a audit interni ed esterni.

Conoscenze

Conoscenza delle normative GMP

Analisi dei dati

Capacità di miglioramento continuo

Teamwork

Formazione

Laurea in discipline scientifiche

Strumenti

MS Office

Descrizione del lavoro

Join to apply for the PQA Support role at Boehringer Ingelheim .

2 days ago Be among the first 25 applicants.

Get AI-powered advice on this job and more exclusive features.

The position

For our site in Fornovo San Giovanni, we are looking for a candidate to join the Quality Assurance Department within a company that produces Active Pharmaceutical Ingredients (APIs) for Human Pharma and Animal Health.

Responsibilities :

• Follow investigation activities related to discrepancies, product non-conformities, returns, complaints, and recalls. Prepare summary reports and monitor the progress of actions, ensuring timely closure of discrepancies and CAPAs.
• Evaluate changes (Change Control management), including issuing related documentation and verifying progress.
• Collaborate on validation of production processes during the industrial phase, reworking, reprocessing, cleaning of production plants, and computerized systems.
• Manage collection, verification, and storage of documentation for each batch (production, quality control, packaging, repackage).
• Collect and evaluate process and analytical data for annual product quality review and ensure timely report issuance.
• Assist in evaluating production processes and identifying improvement opportunities.
• Participate in internal and external audits and support CAPA plans.
• Assist in preparing and issuing SOPs for the Product function.
• Participate in QA training and information programs.

Requirements :

• Approximately 1 year of experience in a similar QA role.
• Knowledge of GMP standards and basic understanding of legal / regulatory requirements.
• Fluent Italian and good English skills (level B2).
• Proficiency in MS Office, especially Excel and PowerPoint.
• Curious, analytical, with a propensity for continuous improvement, innovation, and teamwork.
• Degree in scientific disciplines.

What we offer :

• Temporary 12-month contract via external agency.
• Free access to the company canteen.
• Benefits supporting physical, financial, social, and mental wellbeing.
• Development programs including language learning and professional courses.

Boehringer Ingelheim promotes equal opportunities, respect, trust, and a discrimination-free environment. We value diversity and inclusion, including candidates with disabilities and protected categories under Law 68 / 99.

About us :

We foster a culture that values differences as strengths, supporting your career growth in an authentic, innovative, and respectful environment. We invest in health and wellbeing programs and are committed to making healthcare accessible globally. Join us to help transform lives.

Learn more at .

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Other
• Pharmaceutical Manufacturing

J-18808-Ljbffr