Internship Quality Assurance Operations

Boehringer Ingelheim; Noventa Padovana; In loco; EUR 10.000 - 12.000; Tempo pieno

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

THE INTERNSHIP

The intern will be part of the Quality Assurance Operations team in the Boehringer Ingelheim production site in Noventa Padovana, where veterinary vaccines are produced. The intern will be an active part of Master Batch Record Review in accordance with Eudralex requirements, Process Quality Review for Products. The intern will be trained on the theoretical knowledge of Good Manufacturing Practices and their subsequent application in the technical environment of a pharmaceutical workshop. The intern will acquire skills related to many aspects of Quality Assurance and Compliance in a GMP environment, performing transversal activities in a multinational company context strongly oriented to the sharing of experiences and skills between production sites around the world. Definitely something new to learn every day!

Tasks & what you will be learning:

• Support to the Master Batch Record review.

• Support for the drafting of GMP quality documentation.

• KPI elaboration.

• Interface with production departments.

• Learning of the management system of the Quality.

• Learning procedures applied within the site.

• Review Quality documentation, local and global procedures.

• Preparation and participation to the regulatory inspections.

Requirements:

• 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 Good Manufacturing practice (GMP).

• Good Knowledge of the English language (level B2/C1).

• Good Knowledge of Microsoft Office Package.

• Curious and attitude, propensity for continuous improvement, innovation and teamwork.

• Ability to manage priorities and meet deadlines.

What we offer:

• 6-months curricular/extracurricular internship with possibility of extension.

• Monthly expenses reimbursement of €1.000 with free access to the company canteen.

• A range of benefits for your physical and mental health (access to gyms, psychologist, volunteering and more).

• A support to develop your own professional and personal path that will guide you through our full range of development programs including platforms to learn foreign languages and attend professional courses.

• Constant support and interaction with our specialists and managers.

We warmly welcome applications from candidates belonging to protected categories, in accordance with Law 68/99.

We foster a workplace built on respect, trust, and empathy—free from discrimination. We are powered by our people, and we believe that our differences are our strengths. Everyone is valued, respected and empowered to be themselves.

JOB ID

37516

Job function

Quality

Career level

Entry level & Graduates

Organization

BI AH IT

Working time

Full-Time

Job flexibility

On-Site

Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients, and communities. All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law