Senior Associate, lab Quality Control

July 8 2022
Industries Pharmaceutical, Biotechnology
Categories Chemistry, Laboratory, Pharma, Biotech, Sciences, R&D, Quality assurance and control, Validation
Kirkland, QC

Jubilant HollisterSiter, a subsidiary of Jubilant Pharma Holdings Inc, is currently recruiting for a Senior Associate, Quality Control Laboratory 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 HollisterStier is a rapidly growing company with offices in Kirkland, QC and Spokane, Washington. Our facilities in North America provide specialized manufacturing for the pharmaceutical and biopharmaceutical industries. We provide a full-range of support and services to streamline the manufacturing process such as on-site assistance from process qualifications through product release. Jubilant HollisterStier 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.

Purpose of the job

Transfers, qualifies, and / or validates test methods in compliance with approved protocols and Jubilant standards of active pharmaceutical ingredients, excipients and products in support of new business. Performs stability and routine testing of products.



  • Performs, as per established schedules, chemical analysis and physical testing on assigned samples (development/registration/validation and routine product) by adhering to test methods, protocols, and cGMP / Jubilant standards.
  • Maintains legible and complete records of all test results, instrument readings and observations. Ensures integrity and traceability of all data generated and reported and makes all necessary corrections in accordance with GMP requirements and Jubilant standards.
  • Notifies immediately Supervisor of any out of specification, out of trend, or incomplete testing result, and other irregularities.
  • Provides support to the supervisor in the investigation process.
  • Provides training and act as technical resource for the new analyst.
  • Provides technical support for areas such as: implementation of new methods and / or instrumentation, intra lab transfer, trouble-shooting, training and help in investigation.
  • Performs additional duties as assigned by Management.

Education and Experience

  • DEC or BSc in Analytical Chemistry or closely related discipline.
  • Minimum 10-year experience working in analytical laboratory preferably within quality control or research & development environment. Practical experience in instrumentation (HPLC, GC, UV, IR).
  • Experience in testing different dosage forms such as liquids, creams, lyophilized products, tablets, capsules, and in method troubleshooting.

Skills Required

  • Strong knowledge and application of compendia (USP, EP, BP) and cGMP as it applies to laboratory operations.
  • Solid report writing ability.
  • Computer literacy (Microsoft Office, SAP, and Electronic Data Acquisition System).
  • Bilingual (French & English). Proficiency in English is essential.
Apply now! network