Compliance Specialist - Weekday Nights Mon-Wed; E​/O Thurs

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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.

• 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.

The Compliance Specialist I is responsible for regulatory compliance and quality standards within the manufacturing environment. The role manages a variety of compliance activities, including but not limited to Environmental Monitoring Investigation Reports (EMRs), Environmental Deviation Reports (EDRs), Track Wise deviations, investigation tasks, and area documentation. The specialist ensures investigations, corrective actions, and related tasks are completed accurately, on time, and in alignment with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and established Service Level Agreements (SLAs).

In addition to managing documentation and investigations, the Compliance Specialist partners closely with area specialists, training specialists, and cross‑functional teams to support compliance initiatives, promote audit readiness, and identify opportunities for process improvement. This position requires strong attention to detail, organizational skills, and a proactive approach to driving compliance across the department, ultimately ensuring product quality, regulatory alignment, and patient safety.

• Prepare and manage Environmental Monitoring Investigation Reports (EMRs), Environmental Deviation Reports (EDRs), Track Wise deviations, and investigation tasks in alignment with quality and regulatory requirements.
• Ensure timely completion of investigations, root cause analysis, and corrective/preventative actions (CAPAs) to meet established Service Level Agreements (SLAs).
• Maintain area documentation and records to ensure compliance with GMP, SOP, and applicable regulatory standards.
• Partner with area specialists, training specialists, and cross‑functional teams to support compliance initiatives.
• Provide manufacturing support when required.
• Identify and recommend process improvements to strengthen compliance practices and drive efficiency.
• Support audit readiness by ensuring accurate, complete, and well‑maintained documentation and records.
• Perform additional…