RAW MATERIAL ANALYST

Kymos Group; Ancona; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical field is seeking an Analyst for testing and certification of raw materials. The position involves developing samples and utilizing analytical techniques to ensure adherence to Good Laboratory Practices and GMP standards. Ideal candidates will have a higher education in Laboratory Analysis, experience with HPLC and GC, and a detail-oriented mindset.

Competenze

• 1 year of experience in similar roles in the pharmaceutical industry.
• Experience in GMP environments is an asset.
• Familiar with the use of Pharmacopoeias.

Mansioni

• Developing samples and using analytical techniques to determine physical/chemical properties.
• Performing work in compliance with Good Laboratory Practices and GMP.

Conoscenze

Attention to detail

Analytical techniques

Physical / chemical properties determination

Formazione

Higher education in Laboratory Analysis and Quality Control

Strumenti

HPLC

GC

Descrizione del lavoro

We are looking for an Analyst in testing and certification of raw materials to ensure the correct development of assigned analytical projects.

The responsibilities of the position include :

• Developing samples and using analytical techniques to determine physical / chemical properties.
• Performing the work in compliance with Good Laboratory Practices and GMP.

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

Requirements :

• Higher education in Laboratory Analysis and Quality Control.
• Experience working with HPLC and GC.
• Experience in GMP environments is an asset.
• Skilled in physical / chemical properties determination.
• Familiar with the use of Pharmacopoeias.
• 1 year of experience in similar roles in the pharmaceutical industry.
• Detail-oriented with the ability to achieve objectives.

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