37947_Manufacturing Lead- Weekend Day

Jubilant HollisterStier LLC,u00a0Spokane's Largest Manufacturing Company,u00a0and well-established member of the business community, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. Jubilant HollisterStier is a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant HollisterStier is a proud member of the Jubilant Pharma family.Our Promise: Caring, Sharing, GrowingWe will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions' through growth, cost effectiveness and wise investment of resources.Job Description:Theu00a0Manufacturing Lead,u00a0will have functional responsibility of Aseptic Manufacturing Operations for Line 1 & Line 2 (Preparation, Filtration, Filling, and Lyophilization). Reporting directly to the Manager, Manufacturing, to provide operational support, and maintain a strong working knowledge of the manufacturing processes and equipment within Manufacturing.1. Provide subject matter expertise on Manufacturing processing source materials, equipment and component preparation and sterilization, aseptic filtration, aseptic filling, and lyophilization. Report operational status to the next level of management, and with all affected peers on a daily basis.2. Provide CGMP, job task, and safety training for personnel in the manufacturing areas.3. Order production supplies and equipment required to manufacture product.4. Interact with all supporting departments (ex: Quality Assurance, Maintenance, PIC, etc.) to ensure production line problems are dealt with promptly and with appropriate quality considerations.5. Schedule the validation of processes and equipment.6. Provide subject matter expertise on hourly employee performance, including compliance with SOP's, cGMP's, and safety regulations to the Manager, Manufacturing.7. Work with cross functional teams to review, author and revise standard operating procedures and batch records, assist with conducting deviation investigations, and write deviation reports.8. Document and communicate all aspects of work and leanings, providing training and mentorship for new personnel.9. Ensure that all environmental monitoring limits are maintained in all areas.10. Support and participate in internal and external regulatory inspections as necessary.Qualifications:- Bachelors in a related science field or 2-3 years of relevant experience in lieu of degree required- 2-3 years of relevant experience in an FDA-regulated company required.- Pharmaceutical experience preferred- Production planning desired- Experience in aseptic fill/finish manufacturing desired- Microsoft Word & Excel and Microsoft PowerPoint experience required- Interpretation of cGMP Regulations experience required- Strong attention to detail and organizational skills required- Respirator Clearance required- Work in Aseptic areas required- Prolonged sitting and standing requiredShift:u00a0Weekend days, Friday-Sunday E/O Thursday 6am-6pmCompensation & Benefits:This is anu00a0on-site,u00a0full-time position located in Spokane, WA.

Created: 2026-04-04