Directeur Associé, Services Techniques / Associate Director, Technical Services

Jubilant Pharma, LLC; Montreal; On-site; CAD 90,000 - 150,000; Full time

Job summary

An established industry player is seeking an Associate Director of Technical Services to lead the development and validation of manufacturing processes. This pivotal role involves overseeing technology transfer, providing technical support to manufacturing, and managing a team of scientists and technicians. The ideal candidate will bring over a decade of experience in the pharmaceutical sector, alongside strong leadership skills. Join a rapidly growing company that values diversity and innovation, and contribute to impactful solutions that enhance human health. If you're ready for a rewarding challenge, this opportunity awaits you!

Benefits

Comprehensive medical insurance

Dental insurance

Disability insurance

Collective retirement savings plan

Health and wellness programs

Qualifications

• 10+ years of experience in a related field, with supervisory and managerial roles.
• Experience in the pharmaceutical and FDA regulated industry is essential.

Responsibilities

• Provide technical expertise to develop, validate, and enhance manufacturing processes.
• Manage technology transfer and ensure regulatory compliance.

Skills

Advanced vocational/specialized knowledge

Managing conflict

Influencing outcomes

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Education

Bachelor's Degree in Science, Engineering or related

Job description

Associate Director, Technical Services

Jubilant HollisterStier, a subsidiary of Jubilant Pharma Holdings Inc., is currently recruiting for an Associate Director, Technical Services to join our team!

What do we offer?

A culture that values growth and professional development opportunities, a highly competitive base salary, comprehensive medical, dental, and disability insurance programs, a collective retirement savings plan, and health and wellness programs. Jubilant HollisterStier is a rapidly growing company with offices in Kirkland, Quebec, and Spokane, Washington. A fully integrated contract manufacturing organization, Jubilant HollisterStier has the capability to manufacture sterile injectable preparations, as well as solid and semi-solid dosage forms. Our four facilities in North America and India provide specialized manufacturing services for the pharmaceutical and biopharmaceutical sectors. Jubilant HollisterStier is a proud member of the Jubilant Pharma family. For more information, visit www.jublhs.com.

We will continue, with the utmost care for the environment and society, to enhance value for our customers and stakeholders by delivering innovative products and economically effective solutions through growth, profitability, and judicious investment of resources. If you are ready for a rewarding challenge, we invite you to take the first step and apply today!

Jubilant Pharma Holdings Inc. and all our subsidiaries are proud of the diversity of our workforce. Our goal is to have a workforce as diverse as the patients and customers we serve. We have an inclusive environment where our employees can thrive and where our differences are welcomed. By embracing our differences, we create products that benefit our patients, customers, and human health in general.

Position Objective

The Associate Director of Technical Services is responsible for providing technical expertise to develop, validate, and enhance manufacturing processes.

Key Accountabilities

• Transfer technology for new products from the development site(s) to the manufacturing site.
• Transfer technology to Manufacturing during the process validation of submitted/approved products.
• Plan and manage successive phases of developmental and transfer activities including production of research, Scale-Up, Exhibit/ Registration for ANDA submission, component changes, and process validation batches.
• Provide technical support to manufacturing (i.e. review SOPs, Protocols, reports etc.).
• Perform all supervisory duties including for exempt level scientists and hourly technicians. Assign daily work, hiring, performance management, training, and other managerial duties.
• Write and manage department SOP's, training, etc. to ensure regulatory compliance and operations enhancement.
• Coordinate investigation and closure of incidents.
• Coordinate media fills and related SOP's.

Education Qualification:

• Bachelor's Degree in Science, Engineering or related required.

Experience Required:

• Minimum 10 years of related experience required.
• Supervisory and Managerial experience required.
• Pharmaceutical and FDA Regulated Industry experience required.

Skills Required:

• Advanced vocational/specialized knowledge. Microsoft Word, Excel, and PowerPoint.
• Managing conflict and influencing outcomes.