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QC Chemical Lab Analyst

Lesaffre

Pisticci

In loco

EUR 30.000 - 50.000

Tempo pieno

Oggi
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Descrizione del lavoro

A leading biotechnology company in Italy is seeking a Quality Control Analyst to ensure product quality through detailed chemical analysis and adherence to GMP standards. The ideal candidate holds a Bachelor's degree in Chemistry or Pharmacy, has 1-2 years of experience, and is fluent in both Italian and English. This full-time position offers a temporary contract with a focus on quality assurance in the production process.

Competenze

  • 1-2 years of experience in the same role.
  • Knowledge of GMP and GLP standards.

Mansioni

  • Perform chemical and chemical-physical analysis according to plans.
  • Validate and transfer analytical methods.
  • Perform maintenance and calibration of instruments.

Conoscenze

Fluent in Italian
Fluent in English
Result oriented
Proactive
Relational skills

Formazione

Bachelor’s degree in Chemistry, Pharmacy or Chemistry and Pharmaceutical Technologies

Strumenti

Gas chromatography
HPLC
Karl Fischer
Basic chemical laboratory equipment
SAP
Descrizione del lavoro

For over 30 years, Lesaffre has been involved in Human Health & Nutrition as part of its ambition to Better Nourish and Protect the Planet. In November 2018, Lesaffre acquired Gnosis Advanced Biotech and officially combined it with Lesaffre Human Care to form a new Business Unit named Gnosis by Lesaffre.

At Gnosis by Lesaffre, we are committed to cultivating and delivering nutritional actives, probiotics, and nutritional and functional yeasts that benefit human health and wellbeing, thanks to the power of microorganisms and biotransformation processes like fermentation. Put differently, we explore life to improve living.

Our vision: At Gnosis by Lesaffre, we strive for a world that moves better, digests better, ages better, feels better, and, ultimately, lives better thanks to microorganisms and biotransformation.

Job Description

The QC Department must ensure the Quality Control of all materials, intermediates, final products, according to established specifications and GMP rules. The release of the product is done according to the mentioned rules and to support the QP release.

Responsibilities
  • Perform chemical and chemical-physical analysis, effectively and efficiently, for process controls, input materials, isolated intermediates and finished products, according to predefined plans and specifications, and company quality standards;
  • Perform the analyses provided for in the stability plan;
  • Validate and transfer analytical methods and demonstrate their correct application according to production and quality control requirements;
  • Perform maintenance and calibration of instruments; drafting and/or revision of laboratory SOPs, instrument and process qualification protocols;
  • Cooperate during the external/internal audits;
  • Cooperate during the OOS investigations;
  • Cooperate during the deviation investigations;
Qualifications
  • Bachelor’s degree in Chemistry, Pharmacy or Chemistry and Pharmaceutical Technologies.
  • At least 1–2 years of experience in the same role.
  • Knowledge of GMP and GLP.
  • Knowledge of the following analytical techniques:
    • Gas chromatography
    • HPLC
    • Karl Fischer
    • Basic chemical laboratory equipments
    • SAP (nice to have)
Additional Information
  • Fluent in Italian and English (must have)
  • Result oriented and proactive
  • Sense of urgency
  • Relational skills with the colleagues
  • Full time
  • Temporary Contract
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