Spécialiste, Services Techniques / Specialist, Technical Services

Montreal

Offre publiée le 2025-05-14

Jubilant Pharma, LLC

Choose Gender

Male Female Prefer not to respond

Current Location

Current Organization

Current Designation

Functional Area

Work Experience(in years)

Total Work Experience - Months

Were you referred by a Jubilant Employee

Yes No

Password

Confirm Password

Disclaimer : Jubilant Ingrevia Limited and Jubilant Pharmova Limited collect and use your personal information when you visit our careers webpage. Your personal information is processed in the HR Talent Acquisition system so that Jubilant"s teams can consider and manage your application for the advertised position and contact you. The information you provide to us during the application process may be shared for the purposes of Jubilant"s recruitment program with one or more of Jubilant"s subsidiaries globally.

By clicking the "I Agree" checkbox below you are agreeing to your personal information being processed and used as outlined in our Privacy Policy. For a detailed description on how we process and keep safe your personal data, please see our Privacy Policy at : http : / / www.jubl.com / privacy-policy. You have the right to withdraw your consent or to object to the further processing of your personal information at any time. Further, if you would like to review, correct or update your Personal Information, you can do the same by accessing your profile on our career portal.To delete Personal Information that you have previously provided to us, e-mail us at [email protected].

I Agree

JOB DESCRIPTION

Specialist, Technical Services

Jubilant HollisterSiter, a subsidiary of Jubilant Pharma Holdings Inc. is currently recruiting for a Pharmaceutical Specialist, Technical Services to join our team!

What do we offer?

A culture that values opportunities for professional growth and development, a highly competitive base salary, comprehensive medical, dental and disability insurance programs, a group retirement savings program, health and wellness programs. Jubilant HollisterStier is a fast-growing company with offices in Kirkland, Quebec, and Spokane, Washington. As an integrated contract pharmaceutical manufacturer, Jubilant HollisterStier Subcontracting & Services has the capacity to manufacture sterile injectable formulations, as well as solid and semi-solid dosage forms. Our four facilities in North America and India offer 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 providing innovative products and economically efficient solutions through growth, profitability and wise investment of resources. If you're 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 welcome. By embracing our differences, we create products that benefit our patients, our customers and human health in general.

Purpose of the Job

Process development, focussed primarily on new product introductions of creams and liquids, sterile products, and sterile lyophilised products, including process transfer, development of the working formulae, and process validation.

Responsibilities

  • Evaluate the production process and develop a process suitable to JHS equipment.
  • Initiate appropriate change control documents for new products or for changes to the working formulae of existent products.
  • Prepare the manufacturing formulae and protocols.
  • Train production employees on new formulae and related procedures.
  • Write and execute process validation protocols.
  • Write exception reports if required for validation batches.
  • Develop and control sampling plans.
  • Write interim and final process validation reports.
  • Support investigations
  • Support various departments; Health and Safety, Supply Chain, Quality and Production.
  • Product maintenance including troubleshooting and process improvement.
  • Performs additional duties as assigned by Management.

Education, experience and skills required

  • University degree in Science or Engineering
  • Minimum 2 years experience in Pharmaceutical manufacture
  • Advanced computer and software skills
  • Experience with SAP or other ERP
  • Excellent communication and interpersonal skills
  • Analytical problem solving skills
  • Ability to manage multiple tasks and priorities
  • J-18808-Ljbffr