QC Chemical Lab Analyst

Lesaffre Iberica SA; Prato; In loco; EUR 28.000 - 40.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical sector is seeking a Quality Control Analyst to join their QC Department in Prato. The role involves performing chemical analyses, validating methods, and ensuring compliance with GMP and GLP standards. Suitable candidates should have a Bachelor’s degree in Chemistry or related fields, along with 1-2 years of relevant experience.

Competenze

• 1-2 years of experience in a Quality Control role.
• Knowledge of GMP and GLP standards.
• Experience with analytical techniques like HPLC.

Mansioni

• Perform chemical and chemical-physical analysis on materials and products.
• Validate and transfer analytical methods as per company standards.
• Maintain and calibrate laboratory instruments.

Conoscenze

Knowledge of GMP

Knowledge of GLP

HPLC

Basic chemical laboratory equipment

Formazione

Bachelor’s degree in Chemistry

Bachelor’s degree in Pharmacy

Bachelor’s degree in Chemistry and Pharmaceutical Technologies

Strumenti

SAP

Descrizione del lavoro

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.

Specifically in QC Chemical Lab, your main responsibilities would be :

• 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 :
• HPLC;
• Basic chemical laboratory equipment;
• SAP (nice to have).

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