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

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