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Incoming Inspector, QA

Job in Spokane, Spokane County, Washington, 99254, USA
Listing for: Jubilant Pharma, LLC
Full Time position
Listed on 2026-09-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 28 - 34 USD Hourly USD 28.00 34.00 HOUR
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 QA Incoming Inspector is part of an inspection team responsible for the receipt, sampling, and distribution of samples, inspection, and recommendation of final disposition of components. The Inspector must exercise judgement and make recommendations regarding product acceptance. This position involves interaction with various levels of internal staff as well as contact with vendors, contract clients and various auditors.

  • Handle, inspect, sample and recommend disposition of all incoming raw material components used to process or will become part of the final product.
  • Handle, inspect, sample and recommend disposition of all materials utilized in the laboratory areas such as testing reagents, chemicals, and standards.
  • Inspect, and recommend disposition of all returned goods for Customer Service and carry out that final disposition.
  • Assist in writing and/or revising Standard Operating Procedures and Material Specifications for QA Incoming Inspection area and in the maintenance and control of other records associated with the inspection of incoming materials.
  • Use glassware, which includes back filling of trays during random sampling, qualification of vial test sets, and utilizing the PDA Technical Report 43 for classification of glass defects.
  • Represent the Incoming Inspection area during vendor and client audits/tours of facility and interact with auditors.
  • Other duties as assigned by the department supervisor.

Qualifications:

Required:

  • High School Diploma or Equivalent.
  • Minimum 3 years related experience.
  • Pharmaceutical Experience.
  • FDA Regulated Industry Experience.
  • SAP/Master Control.
  • Travel
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