Jubilant Pharma Limited
Weekend Senior Process Engineer
Jubilant Pharma Limited, Spokane, Washington, United States, 99254
Job Overview
Senior Process Engineer at Jubilant HollisterStier LLC in Spokane, WA. Manufacturer of sterile injectable vials and allergic extracts. Full‑time, on‑site position with competitive base pay ranging from $98,700 to $144,800 annually.
Responsibilities
Design, optimize, and implement site manufacturing processes to improve efficiency, quality, and sustainability.
Oversee and assess existing processes and workflows, establishing and tracking process metrics to monitor stability.
Lead technical transfer of new products from internal and external clients and own the product process from initial quote to retirement.
Perform development work to define critical process parameters (CPPs) and critical quality attributes (CQAs) for robust manufacturing execution.
Author validation study documents and develop/execute validation studies to qualify new and improved processes.
Provide troubleshooting, sampling, and on‑site support during manufacturing events.
Generate and review reports summarizing validation data, identify trends, and recommend corrective actions.
Participate in deviation investigations, implement CAPAs, and support regulatory and client audits.
Collaborate with clean‑room operations to ensure compliance with cGMP, European regulatory requirements, USP chapters, and scientific principles for sterile product manufacturing.
Contribute to continuous improvement of gross profit margin and deviation rate.
Qualifications
Bachelor’s degree in Biology, Chemistry, Physics, or Engineering.
5–10 years of experience in pharmaceutical or FDA‑regulated industry.
Supervisor or leadership experience.
Project management experience.
Master’s degree counts as 2 years of experience.
Statistical analysis and Lean Manufacturing principles desired.
Proficiency with Microsoft Office.
Physical ability to lift 40 lbs unassisted; extended periods of sitting or standing required.
Shift & Schedule Team members may choose between:
4 days at 10 hours per day (Weekends: Friday–Monday or Thursday–Sunday)
5 days at 8 hours per day (Weekends: Wednesday–Sunday, Thursday–Monday, or Friday–Tuesday)
Compensation & Benefits
Base salary $98,700–$144,800 per year, commensurate with experience.
Medical, Dental, Vision, Flexible Spending, Health Savings Accounts.
Life, AD&D, Short and Long‑Term Disability.
401(k) with company match.
Generous paid time off.
Employee Assistance Program.
EEO Statement Jubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For assistance applying, contact HR at JHS‑TalentAcquisition@jubl.com.
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Responsibilities
Design, optimize, and implement site manufacturing processes to improve efficiency, quality, and sustainability.
Oversee and assess existing processes and workflows, establishing and tracking process metrics to monitor stability.
Lead technical transfer of new products from internal and external clients and own the product process from initial quote to retirement.
Perform development work to define critical process parameters (CPPs) and critical quality attributes (CQAs) for robust manufacturing execution.
Author validation study documents and develop/execute validation studies to qualify new and improved processes.
Provide troubleshooting, sampling, and on‑site support during manufacturing events.
Generate and review reports summarizing validation data, identify trends, and recommend corrective actions.
Participate in deviation investigations, implement CAPAs, and support regulatory and client audits.
Collaborate with clean‑room operations to ensure compliance with cGMP, European regulatory requirements, USP chapters, and scientific principles for sterile product manufacturing.
Contribute to continuous improvement of gross profit margin and deviation rate.
Qualifications
Bachelor’s degree in Biology, Chemistry, Physics, or Engineering.
5–10 years of experience in pharmaceutical or FDA‑regulated industry.
Supervisor or leadership experience.
Project management experience.
Master’s degree counts as 2 years of experience.
Statistical analysis and Lean Manufacturing principles desired.
Proficiency with Microsoft Office.
Physical ability to lift 40 lbs unassisted; extended periods of sitting or standing required.
Shift & Schedule Team members may choose between:
4 days at 10 hours per day (Weekends: Friday–Monday or Thursday–Sunday)
5 days at 8 hours per day (Weekends: Wednesday–Sunday, Thursday–Monday, or Friday–Tuesday)
Compensation & Benefits
Base salary $98,700–$144,800 per year, commensurate with experience.
Medical, Dental, Vision, Flexible Spending, Health Savings Accounts.
Life, AD&D, Short and Long‑Term Disability.
401(k) with company match.
Generous paid time off.
Employee Assistance Program.
EEO Statement Jubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For assistance applying, contact HR at JHS‑TalentAcquisition@jubl.com.
#J-18808-Ljbffr