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Process Engineer III

Job in San Francisco, San Francisco County, California, 94199, USA
Listing for: Jubilant Pharma Limited
Full Time position
Listed on 2026-07-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 98700 - 157900 USD Yearly USD 98700.00 157900.00 YEAR
Job Description & How to Apply Below

Jubilant Hollister Stier LLC is a leading pharmaceutical manufacturing company that provides a full range of services supporting life‑changing medicines worldwide.

Job Description
  • Design, optimize and implement site manufacturing processes to improve efficiency, quality and sustainability.
  • Oversee and assess existing processes and workflows.
  • Establish and track process metrics to monitor stability and identify areas for improvement.
  • Provide technical transfer of new products from internal and external clients.
  • Own product processes from initial quote to retirement.
  • Evaluate incoming processes for robustness, efficiency and fit within JHS‑Spokane.
  • Define CPPs and CQAs to enable strong execution upon transfer to manufacturing.
  • Author validation study documents that demonstrate capability to consistently make acceptable product.
  • Develop and execute validation studies to test and qualify new and improved manufacturing processes.
  • Troubleshoot, oversee and/or sample events within manufacturing; occasional off‑shift on‑site support may be required.
  • Generate reports summarizing study results; use data to qualify site processes.
  • Review data summaries from other departments to identify trends or conditions that may impact quality; ensure corrective actions are implemented.
  • Participate in deviation investigations and evaluate impact.
  • Implement effective CAPAs.
  • Optimize gross profit margin and minimize deviation rate.
  • Provide reviews for regulatory and client audits and respond to observation findings.
  • Maintain in‑depth understanding of cGMPs, European regulatory requirements, USP chapters, and scientific principles related to clean room operations and room classifications, including media fills, sterilization, depyrogenation, endotoxin reduction and microbiological monitoring and control.
Qualifications
  • Bachelor’s degree in Biology, Chemistry, Physics or Engineering.
  • 3‑7 years of pharmaceutical or FDA‑regulated industry experience.
  • Leadership or supervisory experience desired.
  • Master’s degree counts as 2‑yr experience.
  • Project Management experience desired.
  • Statistical analysis experience desired.
  • Lean manufacturing principles experience desired.
  • Functional expertise in Project Management and Microsoft Office required.
  • Extended periods of sitting or standing required.
  • Ability to lift 40 lbs. unassisted required.
  • Work in classified/aseptic areas, confined spaces and potential exposure to allergens required.
Location

Spokane, WA — On Site, Full‑Time

Shift

Weekdays

Relocation

Available

Compensation & Benefits

Hiring Wage: $98,700 – $157,900 annually depending on experience, with opportunities for growth, promotion and annual raises. Midpoint and above are reserved for employees who demonstrate outstanding performance and longevity in the role.

  • Medical, Dental & Vision coverage
  • Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
  • Life & AD&D Insurance
  • 401(k) with company match
  • Short‑Term & Long‑Term Disability Insurance
  • Employee Assistance Program
EEO Statement

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.

Contact

JHS‑

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