Specialist - EM
Job in
Spokane, Spokane County, Washington, 99201, USA
Listed on 2026-06-02
Listing for:
Jubilant Bhartia Group
Full Time
position Listed on 2026-06-02
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering
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 Environmental Monitoring department performs the functions associated with sampling, initiating tests, collecting and evaluating test results related to defined quality parameters for surface, air, personnel, product and utility systems such as compressed gases and WFI. The Specialist oversees EM functions and personnel, schedules projects, tasks and personnel, assists in training EM technicians and gown training of all aseptic personnel.
1. Aseptic Certification & Compliance
* Attain and maintain aseptic gowning certification for all designated cleanroom areas.
* Demonstrate consistent compliance with gowning procedures, aseptic techniques, and badge access protocols.
2. Environmental Monitoring Execution
* Perform routine and non-routine environmental monitoring in ISO 8 and sterile manufacturing areas, including gown sampling, area clearance, product sampling, and media fill qualifications.
* Conduct utility sampling (e.g., compressed gases, pass-throughs) and support requalification activities.
3. Sample Preparation & Equipment Handling
* Prepare, autoclave, and manage supplies and equipment required for EM activities, including totes, tubing, labels, documents, and sterile equipment.
* Operate and maintain EM sampling and testing equipment, including sonication and manual verification tools.
4. Data Management & Documentation
* Accurately enter, verify, and trend environmental data using systems such as MODA, Facility Pro, Master Control, and Track Wise.
* Write clear, concise observational memos and ensure data integrity across electronic records and spreadsheets.
5. SOP & Protocol Compliance
* Read, understand, and follow SOPs, protocols, and departmental procedures.
* Participate in the writing, review, and revision of SOPs and protocols to support operational excellence and compliance.
6. Operational Support Across Manufacturing Areas
* Provide EM support during setup, middle-of-run, and end-of-run activities in SVP1, SVP2, CTM, and SLM suites.
* Ensure timely and accurate sampling during production and qualification runs, including gown sampling and sterile suite monitoring.
7. Training & Scheduling Support
* Train or coordinate training for EM personnel, including gowning certification and system use.
* Assist in scheduling EM tasks and personnel in collaboration with the EM Supervisor.
8. Deviation & Change Control Support
* Initiate and support investigations, deviations (Track Wise), TPIRs, and EMIRs as required.
* Contribute to change management processes and maintain compliance with quality systems.
9. Leadership & Backup Responsibilities
* Provide backup support to the EM Supervisor on departmental issues and scheduling.
* Demonstrate initiative in resolving issues, supporting audits, and driving departmental goals.
10. Manufacturing Core Certification
* Must be fully core certified in at least two manufacturing cores.
Full core training in four manufacturing areas is desirable and supports broader operational flexibility
Qualifications:
* High School Diploma required
* Bachelors Of science Preferred
* 2 years Environmental…
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