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Manager, Quality Control

April 22 2020
Industries Pharmaceutical, Biotechnology
Categories Production, Operations, Quality, Safety, Pharma, Biotech, Sciences, R&D, Quality assurance and control, Validation, Chemistry
Kirkland, QC

Jubilant DraxImage, a subsidiary of Jubilant Pharma Holdings Inc, is currently recruiting for a Manager, Quality Control position to join our growing team!

What can we offer?

A 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

We 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.


Establishes and maintains a Quality Control organization which ensures the timely testing of materials and products in accordance with Jubilant DraxImage (JDI) specifications and standards


  • Directs, plans, and provides leadership for the activities of radioactive and non radioactive laboratory personnel to ensure compliance with cGMP regulations and JDI standards.
  • Ensures that all testing (chemical, microbiological, and physical) is conducted in a timely fashion and within approved established framework (SOPs, analytical methods, etc) and that all generated data reflect the commitments to integrity and quality.
  • Generates functional and technically sound validation and stability reports and ensure the timely testing and prompt evaluation of data generated through testing.
  • Recruits and trains staff to carry out functions of the Quality Control Unit. Periodically reviews the performance of direct reports with regards to the achievement of goals, objectives and key performance indicators.
  • Monitors expenses routinely to ensure operations remain within forecasted budgets.
  • Brings to the attention of the Director, Quality Operations and Site Management Committee, information relating to the impact of legislation or any potential critical issues.


  • Minimum B. Sc. in Chemistry, Biochemistry, or closely related discipline.
  • Ten (10) to fifteen (15) years of experience in Quality Control and/or R&D within the pharmaceutical or healthcare industry, with at least five (5) years in a management role. Broad experience with regulatory and ICH standards associated with analytical method validation and qualification and stability.
  • Strong knowledge and application of compendia (USP, Eur.Ph. BP) and cGMP as it applies to laboratory operations.
  • Skilled in problem solving and resolving issues.
  • Detail-oriented with excellent analytical and communication skills.
  • Computer literacy (Microsoft Office, SAP, and Electronic Data Acquisition System).
  • Bilingual (French and English). Proficiency in English is essential. network