Process Engineer III

Jubilant Draxlmage Radiopharmacies Inc, dba Jubilant Radiopharma; San Francisco (CA); On-site; USD 98,700 - 157,900; Full time

Benefits offered by this job

Medical, Dental & Vision coverage

401(k) with company match

Life & AD&D Insurance

Job summary

Jubilant Draxlmage Radiopharmacies Inc, dba Jubilant Radiopharma is seeking a Process Engineer III in San Francisco, CA. This role involves managing large-scale projects and enhancing pharmaceutical processes.

The successful candidate will demonstrate expertise in technical transfers and project management, and possess a Bachelor's degree in Biology, Chemistry, Physics, or Engineering. We offer a comprehensive benefits package and an annual salary ranging from $98,700 to $157,900 depending on experience.

Qualifications

• 3-7 years related Pharmaceutical experience or FDA regulated Industry Experience.
• Supervisory or Leadership Experience is desired.
• Master's Degree counts as 2 years of experience desired.

Responsibilities

• Design, optimize and implement site manufacturing processes.
• Oversee and assess existing processes and workflows.
• Conduct technical transfers of new products.

Skills

Biology

Chemistry

Physics

Engineering

Project Management

Statistical Analysis

Lean Manufacturing Principles

Microsoft Office

Education

Bachelor's Degree in a relevant field

Job description

Process Engineer III – Job Description

The Process Engineer III provides expertise primarily in the area of pharmaceutical process engineering and technical transfer. This position will effectively manage large-scale projects and multi-disciplinary project teams. The process engineer will also provide technical direction for complex projects and exhibit superior communication skills with all levels of employees. This individual will provide leadership and guidance to others.

Responsibilities

• 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 process stability and discover areas for improvement.
• Technical Transfer of new products from both internal and external clients.
• Ownership of product process from initial quote to product retirement.
• Evaluate incoming processes for robustness, efficiency and fit within JHS-Spokane.
• Perform appropriate development work to define CPPs and CQAs to allow strong execution upon transfer to Manufacturing.
• Author validation study documents that demonstrate manufacturing processes are capable of consistently making acceptable product.
• Develop and execute validation studies to test and qualify new and improved manufacturing processes.
• Troubleshooting, oversight and/or sampling of events within Manufacturing will require occasional off‑shift at‑location support.
• Generate reports summarizing results of studies to document data collected; utilize data obtained to qualify site processes.
• Review data summaries generated by other departments, assess the data for potential trends or conditions that may adversely impact the quality of the sterile products being manufactured, and ensure that corrective action measures are implemented when required/warranted.
• Participate in or perform deviation investigation and evaluation of impact.
• Implement effective CAPAs.
• Responsible for optimizing gross profit margin and minimizing deviation rate.
• Provide necessary reviews for regulatory and client audits and provide responses to audit observations.
• In‑depth understanding of cGMPs, European regulatory requirements, relevant USP chapters, and scientific principles associated with clean‑room operations and room classifications as they apply to media fills, sterilization and depyrogenation (dry heat and steam), endotoxin reduction, and microbiological monitoring and control.
• Minimal travel (<10%).

Qualifications

• A Bachelor of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering.
• 3-7 years related Pharmaceutical experience or FDA regulated Industry Experience.
• Supervisory or other Leadership Experience desired.
• Master's Degree counts as 2 years of experience desired.
• Project Management experience desired.
• Statistical Analysis experience desired.
• Lean Manufacturing Principles experience desired.
• Functional expert Project Management required.
• Functional expert Microsoft Office required.
• Extended periods of sitting or standing required.
• Ability to lift 40 lbs. unassisted required.
• Work in classified/aseptic areas required.
• Work in confined spaces required.
• Potential exposure to allergens required.

Location: Spokane, WA – On Site, Full‑Time

Shift: Weekdays

Relocation available

Hiring Wage: $98,700 – $157,900 annually depending on experience, with opportunity for growth, promotion and annual raises. Midpoint and above is reserved for employees who have longevity with Jubilant HollisterStier and consistently exhibit outstanding performance over a period of time in the role.

Benefits

• 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

Jubilant HollisterStier 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.