Laboratory Technician

JR Italy; Nerviano; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

JR Italy is seeking an experienced Laboratory Technician to join their team focused on preclinical formulations. The role involves preparing drug candidates for testing, ensuring compliance with GLP standards, and managing formulation challenges. Ideal candidates should have laboratory experience and good communication skills in English, with an advanced degree in Pharmacy preferred.

Competenze

• Experience working in a GLP qualified facility is desirable.
• Good oral and written communication skills in English are desirable.

Mansioni

• Prepare routine dose formulations for preclinical testing.
• Ensure compliance with GLP guidelines and compile required documentation.
• Identify solutions in case of formulation issues.

Conoscenze

Laboratory work experience

Communication skills in English

Formazione

Advanced degree in Pharmacy/CTF

Descrizione del lavoro

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About the position: Preclinical Formulations – Laboratory Technician

We are looking for an experienced Laboratory Technician to expand the current Staff dedicated to the formulation of drug candidates to be assessed in preclinical safety studies.

About Accelera

Accelera is a Preclinical CRO (Contract Research Organization) and offers unparalleled expertise in bringing innovative drug candidates from the Discovery to the Clinical Phases.

Over the years, Accelera has brought new products and innovative therapies to the market, supporting overall more than 300 Companies and Sponsors worldwide.

Accelera operates in strict compliance with the International recognized quality standards (Good Laboratory Practices), to ensure the smoothest development of innovative therapies intended to improve the quality of life of patients worldwide.

Job Function Tasks

• Prepare routine dose formulations for preclinical testing.
• Contribute to the timely execution of the experimental phases, providing GLP qualified formulation of the test item(s) under investigation.
• Contribute to formulation activities on test items provided by different Sponsors, and identify solutions in case of formulation issues (poor solubility, stability, drugability, etc)
• Take care of equipment according to respective SOPs, and of full documentation of routine maintenance and repairs.

Ensure full compliance with the GLP guidelines.

• Compiling GLP/no--GLP notebooks and documents according to and the GLP guidelines.
• Keep full GLP compliant record of delivery/use/archiving/transfer/destruction of test item(s)

Required Qualification

• Laboratory work experience is preferred.
• An advanced degree in Pharmacy/CTF or similar is preferred but not strictly required.
• Experience working in a GLP qualified facility is desirable.
• Good oral and written communication skills in English are desirable.