QA Operations Internship - Master Batch Records in GMP

Boehringer Ingelheim

Noventa Padovana

In loco

EUR 10.000 - 12.000

Tempo pieno

7 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura completa in un minuto — curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

€1,000 monthly reimbursement
Free canteen access
Health & development programs

Descrizione del lavoro

Boehringer Ingelheim in Noventa Padovana invites applications for a 6-month curricular internship in Quality Assurance Operations. You will participate in Master Batch Record Review, GMP documentation, and KPI analysis under global QA guidelines.

We seek a Master’s degree in Chemistry, CTF, Pharmaceutical or Biology, strong organizational skills, teamwork, and good English (B2/C1). The program offers training, exposure to regulatory inspections, and access to development platforms.

Competenze

  • Master’s degree in Chemistry, CTF, Pharmaceutical or Biology.
  • Good organizational skills and ability to work in team/individually.
  • Ability to work methodically and carefully according to tight deadlines.
  • Knowledge of European Pharmacopeia and GMP.
  • Good knowledge of English (B2/C1).
  • Proficiency with MS Office.

Mansioni

  • Support Master Batch Record review.
  • Assist in drafting GMP quality documentation.
  • Elaborate KPIs.
  • Interface with production departments.
  • Learn QA management systems and site procedures.
  • Prepare for regulatory inspections.

Conoscenze

Organizational skills
Teamwork
Ability to work methodically
Prioritization
English proficiency
MS Office

Formazione

Master’s degree in Chemistry, CTF, Pharmaceutical or Biology

Strumenti

Microsoft Office

Descrizione del lavoro

Boehringer Ingelheim in Noventa Padovana invites applications for a 6-month curricular internship in Quality Assurance Operations. You will participate in Master Batch Record Review, GMP documentation, and KPI analysis under global QA guidelines.

We seek a Master’s degree in Chemistry, CTF, Pharmaceutical or Biology, strong organizational skills, teamwork, and good English (B2/C1). The program offers training, exposure to regulatory inspections, and access to development platforms.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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