Jubilant DraxImage, a subsidiary of Jubilant Pharma Holdings Inc, is currently recruiting for an Analytical & NPI Supervisor, 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 www.draximage.com
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.
The Analytical and NPI Specialist for the Quality Control department is responsible for the QC planning for successful technical transfer of new products and analytical methods to the QC laboratories. This individual will also be responsible for the introduction of new equipment and software to the Quality Control department. The Analytical and NPI Specialist will maintain compliance of the quality control activities for documentation and instrumentation to the internal standard operating procedures, pharmacopeias and those of the regulatory agencies (HPFBI, FDA, EU, etc.).
Co-ordinate the technical transfer of new products and analytical methods to the QC laboratory. Participate in project meetings, approve assessments, protocols and reports, provides guidance to the QC laboratory during troubleshooting.
Recommends instrument purchasing/replacement in a cost effective manner that leads to higher quality and efficiency in compliance with cGMP practice.
Defines scope of project for introduction of new equipment and software for the QC laboratories. Assemble cross-functional teams (IT, Validation, Quality, etc), detail plan and prioritize the tasks in order to achieve project goals.
Directs, plans, and provides leadership for the Quality Control documentation activities (SOP, analytical methods, validation/qualification and analytical assessments) and data integrity to ensure compliance with internal standards and regulatory requirements.
Performs any other tasks assigned by Management.
Minimum of ten (10) years of experience in Quality Control and/or R&D within the pharmaceutical or healthcare industry,
Strong project management skills.
Broad experience with regulatory and GMP standards associated with analytical method validation and instrument qualification.
Thorough understanding of the pharmaceutical development process that leads through to commercial manufacturing and the associated GMP requirements.
Detail-oriented with excellent analytical and communication skills.
Computer literacy (Microsoft Office, SAP environment, and Electronic Data Acquisition System).
Member of the Ordre des Chimistes du Québec
Bilingual (French and English). Proficiency in English is essential