Supervisor, Quality Control - Jobs in Kirkland, QC

Job Description

Jubilant DraxImage, a subsidiary of Jubilant Pharma Holdings Inc, is currently recruiting for a Supervisor, Quality Control position to join our growing team!What can we offerA culture that values opportunity for professional growth and development,highly competitive base pay, comprehensive medical, dental and disability benefits programs, group retirement savings program, health and wellness programs.Jubilant DraxImage Inc. is a rapidly growing company with offices in Kirkland, QC and Yardley, PA. A global leader in the development of radiopharmaceuticals and state-of-the-art technologies, we are continuously seeking high caliber professionals to join our team. Jubilant DraxImage is a proud member of the Jubilant Pharma family. For more information, visit www.draximage.comWe will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions’ through growth, cost effectiveness and wise investment of resources.If you’re up for a rewarding challenge, we invite you to take the first step and apply today!Jubilant Pharma Holdings Inc and all our subsidiaries proudly embraces diversity in our workforce. Our goal is to have a workforce as diverse as the patients and clients we serve. We have an inclusive environment where our employees can thrive and where our differences are welcomed. By welcoming our differences, we create products that are beneficial for our patients, clients, and overall human health.Purpose of the jobEstablishes and manages laboratory activities within the Quality Control department to ensure that all manufactured products are tested to Jubilant DraxImage Inc. specifications and regulatory requirements.ResponsabilitiesPlans, schedules and supervises the review of samples (finished products, raw materials, components, packaging intermediates, stability and validation samples) in a timely manner. Determines and coordinates the assignment of tasks to be performed by laboratory personnel.Schedules the gathering of analytical data for the APQR and reviews the APQRConducts investigations of Out-Of-Specifications (OOS), Out-of-Trends (OOT) and quality incidents within established time frames and produces investigation reports.Reviews and approves all analysis related documents in a timely manner. Maintains documents in good order related to testing operations and in accordance with Jubilant DraxImage 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.Recruits and trains personnel to perform all QC laboratory functions. Periodically reviews staff performance in achieving goals, objectives and key performance indicators.Performs other duties as assigned by management.Education and ExperienceMinimum of a B.Sc. in analytical chemistry, biochemistry or related discipline.Must be a member of the Quebec Order of Chemists.Minimum five (5) years experience in a quality control laboratory in a pharmaceutical environment. Extensive experience in laboratory and instrumentation work.Experience in a radioactive environment is an assetSkills RequiredWorking knowledge of pharmacopoeias (USP, Ph. Eur. and BP) and Good Manufacturing Practices (GMP) and their application in a laboratory settingComputer knowledge (Microsoft Office, SAP and electronic data acquisition system).Knowledge of microbiology is an asset.Bilingual (French and English). Fluency in English is essential.Strong interpersonal, organizational, communication and report writing skills.Quick Apply

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