Quality Control Raw Materials Analyst

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

Descrizione del lavoro

A leading pharmaceutical company in Fornovo San Giovanni seeks a Quality Control Raw Materials Analyst. Responsibilities include performing analytical tests, ensuring compliance with safety standards, and writing procedures. The ideal candidate has a chemistry background and experience in quality control. This role offers a temporary contract, a supportive work environment, and various benefits for employee wellbeing.

Servizi

Free access to company canteen

Access to gyms and psychological support

Professional development programs

Parental support and volunteering opportunities

Competenze

• 1-5 years of experience in the chemical-pharmaceutical quality control field is preferred.
• Willingness to work in shifts, including occasionally Saturdays and Sundays.

Mansioni

• Independently performs analytical testing required for the release of raw materials.
• Ensures adherence to quality procedures.
• Writes protocols, reports, and procedures.

Conoscenze

Quality control equipment knowledge

Analytical discrepancy management

Teamwork

Good understanding of written English

Formazione

Educational background in chemistry or related fields

Strumenti

Gas chromatographs

HPLC

Potentiometric titrators

Spectrophotometers

Atomic absorption/ICP‑MS

Laboratory data management software

Descrizione del lavoro

Apply for the Quality Control Raw Materials Analyst role at Boehringer Ingelheim.

The Position

We are looking for a Quality Control Analyst for our Raw Materials Team, to support the increased analytical activities related to the introduction of a New Chemical Entity and to ensure compliance standards required by corporate and international authorities.

Tasks & Responsibilities

• Reports directly to the Raw Materials Coordinator
• Independently performs analytical testing required for the release of raw materials used in the synthesis of finished and semi‑finished products and in the in‑process controls
• Ensures the correct procedures are adhered to, in terms of Quality, Environment & Safety
• Raises and investigates deviations and out of specifications within the QC department
• Promotes, develops, and strives for continuous process improvements within the QC department including method development and evolving existing processes
• Writes Protocols, Reports and Procedures (SOPs); learns the management system of the Quality Learning tools and procedures applied within the site
• Executes all assigned activities in compliance with established analytical procedures
• Collaborates with the intermediate product release team when needed

Requirements

• Educational background in chemistry or related fields
• 1-5 years of experience in the chemical‑pharmaceutical quality control field is preferred
• Good knowledge of the main equipment used in quality control laboratories, particularly gas chromatographs (direct injection and Head‑Space), HPLC, potentiometric titrators, spectrophotometers, and atomic absorption/ICP‑MS
• Knowledge of analytical discrepancy management workflows (OOX / Event / Deviations) and regulatory requirements in the pharmaceutical industry (GMP / ISO)
• Familiarity with laboratory data management software
• Good understanding of written English
• Willingness to work in shifts, including occasionally Saturdays and Sundays
• Teamwork attitude

What we offer

• A temporary contract with an external agency (24 months – Somministrazione)
• Free access to the company canteen and ticket restaurants when working remotely.
• A range of benefits for physical, financial, social and mental wellbeing (access to gyms, psychologist, volunteering, parental support, company welfare 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.

Equal Opportunity Statement

We are committed to guarantee equal opportunities; we believe in respect, trust and empathy, in a work environment without discrimination. We are powered by our people as we know that our differences are our strengths. We value everyone and each of us feels included, important and at ease.

This job requisition is addressed also for candidates with disabilities and belonging to protected categories following articles 1 and 18, Law 68/99.

Job Information

• Seniority level: Mid‑Senior level
• Employment type: Full‑time
• Job function: Quality Assurance
• Industries: Pharmaceutical Manufacturing