Supervisor II, Manufacturing
Job in
Spokane, Spokane County, Washington, 99254, USA
Listed on 2026-07-20
Listing for:
Jubilant Pharma Limited
Full Time
position Listed on 2026-07-20
Job specializations:
-
Manufacturing / Production
Production Manager, Regulatory Compliance Specialist, Production QC/QA
Job Description & How to Apply Below
Job Title
Manufacturing Supervisor II
LocationSpokane, WA – On Site, Full‑Time
ShiftMonday‑Friday, 7:00 AM – 4:30 PM
Compensation & BenefitsHiring Wage: $89,300.00 – $. Benefits start day one and include Medical, Dental & Vision coverage, Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), Life & AD&D Insurance, Short‑Term & Long‑Term Disability, and Employee Assistance Program.
Responsibilities- Supervise assigned manufacturing operations including processing source materials, equipment and component preparation and sterilization, aseptic filtration, aseptic filling, lyophilization, inspection, and packaging.
- Report operational status to management and peers daily.
- Review and update manufacturing documentation.
- Provide cGMP, job task, and safety training for personnel in the manufacturing areas.
- Generate, update and maintain area Standard Operating Procedures and BPRs. Ensure compliance with cGMP through observation, training and auditing.
- Supervise hourly employee performance, ensuring compliance with SOPs, cGMPs and safety regulations.
- Perform deviation investigations and implement corrective actions to prevent recurrence.
- Order production supplies and equipment required to manufacture products.
- Prepare production‑monitoring reports and participate in analysis of product cost and budgeting process.
- Interview new employees, provide coaching and counseling, conduct performance evaluations, and set objectives and performance standards.
- Assist upper management in implementing disciplinary action when necessary.
- Analyze and make recommendations regarding capital expenditures and efficiency improvements.
- Collaborate with supporting departments (Quality Assurance, Maintenance, PIC, etc.) to resolve production line problems with appropriate quality considerations.
- Schedule validation of processes and equipment.
- Ensure all environmental monitoring limits are maintained in all areas.
- Bachelor of Science in Biology, Chemistry or related hard science required.
- 2 years of related leadership experience is acceptable in lieu of a hard science degree, or four years of solid pharma manufacturing or related supervisory experience in lieu of a degree.
- 1 to 5 years of related experience required.
- Lead experience required.
- Supervisory experience preferred.
- Pharmaceutical experience preferred.
- Microsoft Word and Excel required.
- Microsoft PowerPoint required.
- Interpretation of cGMP regulations required.
- Ability to manage conflict and influence outcomes required.
- Basic communication skills required.
- Problem‑solving skills required.
Jubilant Hollister Stier is an EEO/AA Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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