Specialist, QA Auditor

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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.

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 main function of the QA Auditor, Specialist & senior Specialist is to coordinate personnel to support the CMO & ABU production schedule. This person will work closely with peer training specialists to ensure compliance with cGMPs prior to assigning personnel to areas. The QA Auditor, Specialist is the department SME and will have in depth knowledge of area SOPs to help guide personnel throughout the production day.

They are also expected to analyze, present and propose department processes and technologies to determine improvements to processes, equipment, and automation to optimize processes, meet present and new regulations, reduce waste, increase capacity, and develop and implement methods to increase output while complying with cGMP's. The QA Auditor Specialist will qualify to perform all QA Auditor tasks and processes.

• Complete inspector qualification program for manual and semi-automated inspection; qualification must be maintained annually.
• Process final container samples; perform inspection/sampling according to SOP, Protocol or client request memo.
• Read and follow established Standard Operating Procedures covering execution and documentation of QA Auditing processes.
• Complete accurate documentation of QA Auditing processes on production records using GDP.
• Assure that labeling and packaging lines are clean and free of materials and components from previous lots.
• Perform visual inspection of product vials and packaging over extended periods of time (12 hours/day, with appropriate breaks).
• Assure that through a system of auditing that cGMPs are followed in manufacturing and finished product packaging areas.
• Provide effective day-to-day leadership and oversight for small groups ranging in size from 5 to 10 team members.
• Schedule team members proficiently to achieve target turnaround times and meet production schedule targets.
• Area SME for SOP updates and proposed equipment/process changes.
• Partner with training peers to drive training of team members.
• Write clear, concise memos for associated…