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Validation Engineer II​/III​/Sr

Job in Spokane, Spokane County, Washington, 99254, USA
Listing for: Jubilant Pharma, LLC
Full Time position
Listed on 2026-09-17
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer, Quality Engineering, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 89300 - 163300 USD Yearly USD 89300.00 163300.00 YEAR
Job Description & How to Apply Below

Jubilant Hollister Stier Spokane is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
For our EEO Policy Statement, please . If you’d like more information on your EEO rights under the law, please .

JOB DESCRIPTION

Join a Leader in Pharmaceutical Manufacturing — And Build What’s Next

As Spokane’s Largest Manufacturing Company
, Jubilant Hollister Stier LLC is a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support life changing medicines around the world.
We are nationally recognized for our expertise in producing sterile injectable vials and lyophilized products, and our Allergy business is a global leader in allergenic extracts that support treatments for allergies and asthma. Jubilant Hollister Stier is proudly part of the global, Jubilant Pharma family. established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support life changing medicines around the world.

For the Builders, Innovators, and Doers — This Is Your Place

If you are someone who thrives on solving complex problems, improving systems, and building real solutions
, you’ll feel at home here. At Jubilant Hollister Stier, your ideas matter — and your impact is felt globally.

Why builders choose us:

  • Immediate impact: Your work directly supports essential medicines and allergenic therapies used worldwide.
  • Benefits start on day one: Medical, Dental, Vision, FSA/HSA, Life, AD&D, and Disability benefits begin immediately because your well-being shouldn’t have a waiting period.
  • A career you can grow: We provide opportunities for growth, promotion, and annual raises, with midpoint compensation reserved for high performance and longevity.
  • A culture of improvement: We value people who thrive on continuous improvement, innovation, and hands on contribution.
  • A stable industry leader: Backed by Jubilant Pharma, we pair long term stability with forward looking innovation.

If you want to build something meaningful with a team that values your drive, skills, and ideas —
you belong here.

Job Description:

The Validation Engineer provides pharmaceutical process validation knowledge and technical engineering activities within pharmaceutical Commercialization, Development, & Optimization (CDO), with focus areas that may include steam sterilization, lyophilization, aseptic processing, mixing operations, cleaning processes, and related GMP manufacturing systems. The engineer will also contribute technical direction for CDO opportunities and exhibit clear communication skills with all levels of employees and external customers.

Responsibilities may vary by level and assignment. The accountabilities below describe the general scope of work for the job profile and are not intended to be a comprehensive list of all duties that may be assigned.

  • Provides technical support for CDO and engineering opportunities, including process characterization, process boundary testing, process compliance upgrades, cost reduction, contract manufacturing, process improvements, facility/utility impacts, construction projects, and related technical initiatives.
  • Through education and experience, applies pharmaceutical engineering validation judgment to evaluate technical feasibility, define engineering requirements, support process/equipment troubleshooting, and recommend practical solutions for CDO-related opportunities and pharmaceutical systems.
  • Is responsible for assistance in contributing knowledge of regulatory requirements for the…
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