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Spécialiste, Services Techniques / Specialist, Technical Services

Jubilant Pharma, LLC

Montreal

On-site

CAD 60,000 - 100,000

Full time

9 days ago

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Job summary

An established industry player is seeking a Pharmaceutical Specialist for Technical Services to enhance their production processes. This role involves developing new product introductions, including creams and sterile products, and requires a strong background in science or engineering. You will evaluate production processes, prepare manufacturing protocols, and train staff on new procedures. Join a fast-growing company that values professional growth, diversity, and innovative solutions in the pharmaceutical sector. If you're ready for a rewarding challenge, apply today!

Benefits

Comprehensive medical insurance
Dental insurance
Disability insurance
Group retirement savings program
Health and wellness programs

Qualifications

  • Minimum 2 years experience in Pharmaceutical manufacture.
  • University degree in Science or Engineering required.

Responsibilities

  • Evaluate and develop production processes suitable for equipment.
  • Prepare manufacturing formulae and protocols.
  • Train production employees on new formulae.

Skills

Analytical problem solving skills
Excellent communication skills
Interpersonal skills
Advanced computer skills
SAP or other ERP experience

Education

University degree in Science
University degree in Engineering

Tools

SAP
ERP systems

Job description

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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
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