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Quality Control Raw Materials Analyst

Job in Flowood, Rankin County, Mississippi, 39232, USA
Listing for: Boehringer Ingelheim GmbH
Seasonal/Temporary, Contract position
Listed on 2026-02-12
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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

Responsibilities:
  • Reports directly to the Raw Materials Coordinator.
  • Independently performs analytical testing required for the release of raw materials used inthe synthesis of finished and semi-finished products and in the in-process controls.
  • You will ensure the correct procedures are adhered to, in terms of Quality, Environment & Safety.
  • You will raise and investigate 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
  • You will write Protocols, Reports and Procedures (SOPs) Learning of 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.
  • 1-5 years of experience in chemical-pharmaceutical quality control field is considered a preferred.
  • Good knowledge of the main equipment used in quality control laboratories is required, particularly gas chromatographs (both direct injection and Head‑Space), HPLC, potentiometric titrators, spectrophotometers, and atomic absorption/ICP‑MS.
  • Knowledge of analytical discrepancy management workflows (OOX / Event / Deviations) and knowledge of 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.
What we offer
:
  • For this position we offer a temporary contract with an external agency (24 Mesi - Somministrazione).
  • Free access to the company canteen and ticket restaurants when working remotely.
  • A range of benefits for you 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.

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.

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