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Associate, Stability

Job in Spokane, Spokane County, Washington, 99254, USA
Listing for: Jubilant HollisterStier LLC
Full Time position
Listed on 2026-09-03
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Engineering, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 32.01 - 37.65 USD Hourly USD 32.01 37.65 HOUR
Job Description & How to Apply Below

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 purpose of the Stability Associate is to implement required new studies, maintain the stability study program for all products that require such testing, generate related protocols, maintain Standard Operating Procedures (SOPs), and communicate with contract clients as it relates to the stability program. In addition, the Stability Associate will assist in maintaining compliance with the Jubilant Hollister Stier Stability Program and provide support in actions required due to power outages and temperature/humidity excursions for stability chambers.

  • Maintain the stability program for the products which require such testing. This includes:
    • Ensure that stability batches are provided to the stability department in a timely basis and studies are initiated as required by the appropriate protocol or SOP.
    • As required, enter stability data into the Stability LIMS System and review stability data.
    • Provide required reports as scheduled (Annual Reviews, DMFs, client product reports) or more frequently upon request.
    • Document significant events for stability studies and communicate issues to internal/external stakeholders, as directed.
    • Maintain clear chain of stability sample custody and accurate inventory.
    • Review completed or cancelled studies. Close out studies as required.
  • Revise existing SOPs or create new SOPs as required to document stability department processes.
  • Write study plans, protocols, and deviations, as directed.
  • Research and summarize stability data to assist in resolution of customer complaints, as required.
  • Conduct special projects as directed by the QC Stability Supervisor and/or Manager, such as summarize
  • information on product deviations, failures, or process changes.
  • Work with the QC Stability Supervisor and/or Manager, facilities maintenance, business development, and
  • process development and other personnel to ensure adequate space is available for stability sample storage.
  • Assist with activities to ensure compliance related to Stability areas as directed by the QC Stability Supervisor and/or Manager, including assessment/actions related to chamber temperature/humidity excursions.
  • Assist with stability related Deviation investigations.
  • Qualifications:

    Required:

    • High School diploma or equivalent plus 2 years of pharmaceutical experience or FDA regulated industry experience is required.
    • Working Knowledge of Microsoft Word and Microsoft Excel

    Preferred:

    • Bachelor's Degree
    • Understanding of cGMP concepts, especially as related to stability studies and quality.
    • Familiarity with the FDA and ICH guidelines for conducting stability studies.
    • Basic understanding of various computer programs, which may be used to establish the databases and evaluation methods of the data.
    Working Environment:
    • Prolonged sitting
    • Lifting up to 25 lbs

    Location:
    Spokane, WA
    - On Site, Full-Time

    Shift: Monday-Friday 8am-5pm

    Compensation & Benefits That Start on Day One
    - Because Your Well Being Matters

    Hiring Wage: $32.01 - $37.65 hourly, with opportunities for growth, promotion, and annual raises.

    At Jubilant Hollister Stier, we don't believe in waiting periods. From the moment you…

    Position Requirements
    10+ Years work experience
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