Homeland

Principal Process Engineer
Engineering
SpokaneWashington Direct Hire Jun 16, 2026

Job Summary
Homeland Talent Solutions is partnering with a leading pharmaceutical manufacturing organization to identify a Principal Process Engineer to support continued growth, product expansion, technology transfer initiatives, and operational excellence efforts within a highly regulated manufacturing environment.

The Principal Process Engineer will serve as a site-wide technical authority responsible for supporting pharmaceutical manufacturing operations, technology transfer programs, process optimization initiatives, validation efforts, and client-facing technical discussions. Working closely with Manufacturing, Quality, Validation, Regulatory Affairs, Technical Services, and Executive Leadership, this individual will lead high-priority projects that directly impact product commercialization, manufacturing performance, and long-term business success.

This highly visible Principal Process Engineer position offers the opportunity to influence manufacturing strategy, lead complex technology transfer initiatives, mentor engineering talent, and serve as a trusted advisor to both internal leadership and external clients. The ideal candidate is a collaborative technical leader who enjoys solving complex challenges, driving continuous improvement, and making a meaningful impact on products used by patients worldwide.

Responsibilities

  • Serve as a site-wide subject matter expert in pharmaceutical process engineering
  • Provide strategic leadership for manufacturing process design, optimization, and continuous improvement initiatives
  • Evaluate manufacturing processes for scalability, robustness, efficiency, and regulatory compliance
  • Drive technical problem-solving efforts supporting manufacturing operations
  • Support long-term process ownership and product lifecycle management strategies
  • Lead multiple concurrent technology transfer projects and assess incoming products for successful site implementation
  • Support new product introductions and manufacturing scale-up initiatives
  • Partner cross-functionally to ensure successful product transfers and commercialization efforts
  • Author, review, and oversee validation protocols, reports, and supporting technical documentation
  • Support process validation strategies and execution activities
  • Lead investigations, deviations, change controls, and corrective action initiatives
  • Ensure compliance with cGMP regulations and pharmaceutical manufacturing requirements
  • Support regulatory inspections, audits, and client reviews
  • Serve as the primary technical representative during client-facing meetings and technical discussions
  • Present technical recommendations and support strategic decision-making initiatives
  • Mentor and develop Process Engineers and Technical Services team members
  • Provide technical guidance across multiple departments and support organizational initiatives as needed
  • Serve as a delegate for Technical Services leadership during client meetings, project reviews, and operational discussions

Requirements
  • Bachelor's degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, or a related technical discipline
  • 10+ years of pharmaceutical manufacturing, biopharmaceutical manufacturing, or FDA-regulated industry experience
  • Expert-level process engineering and technology transfer experience
  • Experience supporting manufacturing operations within regulated manufacturing environments
  • Strong project leadership and cross-functional collaboration skills
  • Excellent technical communication, presentation, and problem-solving abilities
  • Prior leadership, mentoring, or supervisory experience
  • Master's degree or PhD, preferred
  • Sterile injectable manufacturing experience, preferred
  • Aseptic processing experience, preferred
  • Process validation expertise, preferred
  • Statistical analysis and process capability experience, preferred
  • Lean Manufacturing and Continuous Improvement experience, preferred
  • CDMO or contract manufacturing experience, preferred


Benefits
This role offers a competitive annual salary of $130,275–$208,400, along with a comprehensive benefits package. Benefits begin on day one and include medical, dental, and vision coverage, HSA and FSA options, life and AD&D insurance, short- and long-term disability coverage, and an Employee Assistance Program. Employees also benefit from ongoing career development opportunities, annual compensation reviews, and clear paths for professional growth and advancement.

Summary
Join a growing pharmaceutical manufacturing leader where your expertise will drive innovation, operational excellence, and the delivery of life-changing therapies to patients around the world. Lead high-impact initiatives, influence strategic decisions, and make a lasting impact on the future of the organization. Apply today!



EEO Notice
Homeland LLC is an Equal Opportunity Employer. Homeland LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Homeland LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Reasonable accommodation is available for qualified individuals with disabilities, upon request.
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