Superviseur I, Control Qualité / Supervisor I, Quality Control

at  Jubilant DraxImage Inc

QUALIFICATIONS :

• Titulaire d’un baccalauréat en en chimie analytique, biochimie ou discipline reliée.
• Membre de l’ordre des Chimistes du Québec.
• Minimum trois (3) ans d’expérience dans un laboratoire de contrôle de la qualité en gestion en milieu pharmaceutique. Vaste expérience dans les travaux de laboratoire et d’instrumentation.
• Expérience d’environnement radioactif, un atout.
• Communication écrite et verbale, avec une compétence bilingue en anglais et en français.
• Connaissances informatiques (Microsoft Office, SAP).

QUALIFICATIONS:¿

• Bachelor’s degree in analytical chemistry, biochemistry or related discipline.
• Member of the Quebec Order of Chemists.
• Minimum three (3) years’ experience in a pharmaceutical quality control laboratory. Extensive experience in laboratory work and instrumentation.
• Experience in a radioactive environment is an asset.
• Written and verbal communication skills, with bilingual competence in English and French.
• Computer skills (Microsoft Office, SAP).

JOIN US:¿¿

If you are looking for a challenging yet rewarding opportunity to make a difference in the healthcare industry, we invite you to apply for the Supervisor 1, Quality Control position at Jubilant Radiopharma. Join us in our mission to deliver innovative solutions that enhance patient care and improve lives. Apply now and be part of our success story!¿
Job Overview

ROLE OVERVIEW:¿¿

As Supervisor I, Quality Control, you establish and manage laboratory activities within the Quality Control organization to ensure that all manufactured products are tested according to Jubilant DraxImage Inc. specifications and regulatory authority requirements.

KEY RESPONSIBILITIES:¿

• Plans, schedules and supervises the analysis of samples (finished products, raw materials, components, packaging intermediates, stability and validation samples) within a reasonable timeframe. Determines and coordinates the assignment of laboratory tasks.
• Plans the collection of analytical data for the APQR report and reviews the APQR report.
• Investigates “Out-Of-Specifications” (OOS), “Out-of-Trends” (OOT) and quality incidents within established timeframes and produces investigation reports.
• Ensures the integrity and accuracy of GMP-compliant documents. Reviews and approves all analysis-related documents (CofA). Maintains documents in good order relating to operations testing and in compliance with DraxImage Jubilant record retention schedule.
• Recommends the purchase/replacement of instruments in a cost-effective manner that leads to a higher level of quality and efficiency in accordance with cGMP standards.
• Participates in the recruitment and training of laboratory staff. Periodically reviews staff performance in achieving goals, objectives and key performance indicators.