Process Engineer III

Jubilant HollisterStier Spokane

$98K — $157K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biology, Chemistry, Physics, or Engineering required.
  • 3-7 years of pharmaceutical or FDA regulated industry experience required.
  • Supervisory or leadership experience desired.
  • Master's degree counts as 2 years of experience desirable.
  • Project management and statistical analysis experience desired.
  • Experience with Lean manufacturing principles desired.
  • Proficient in Microsoft Office and project management functions required.

Responsibilities

  • Design and implement site manufacturing processes to enhance efficiency and quality.
  • Oversee existing processes and workflows to identify improvement areas.
  • Establish and track process metrics for stability and improvements.
  • Lead technical transfer of new products from clients and internally.
  • Author validation study documents for manufacturing processes.
  • Conduct validation studies for new and improved manufacturing techniques.
  • Participate in deviation investigations and implement CAPAs.

Benefits

  • Comprehensive medical, dental, and vision coverage from day one.
  • Flexible Spending Accounts (FSA) and Health Savings Accounts (HSA) available.
  • Life and AD&D insurance included.
  • 401(k) plan with company matching contributions.
  • Short-term and long-term disability insurance offered.
  • Employee Assistance Program provided.
Full Job Description
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.
  • 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 cGMP's, 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's of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering is required.
  • 3-7 years related Pharmaceutical experience or FDA regulated Industry Experience required.
  • Supervisory or other Leadership Experience desired.
  • Master's Degree counts as 2 yrs 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

Compensation & Benefits That Start on Day One - Because Your Well Being Matters

Hiring Wage:

This is an on-site, full-time position located in Spokane, WA.
  • 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.

At Jubilant HollisterStier, we don't believe in waiting periods. From the moment you join us, you and your family have access to a full suite of benefits designed to support your health, stability, and long-term success.

Starting on your first day, you receive:
  • 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

Unlock Your Potential

If you're seeking a dynamic and rewarding career, we welcome your application today. Apply online:

Careers - Jubilant HollisterStier

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