Senior Validation Engineer — GMP Process Validation

Jubilant Pharma, LLC; Spokane (WA); On-site; USD 89,000 - 163,000; Full time

Benefits offered by this job

Medical, Dental & Vision coverage

FSA/HSA

Life & AD&D Insurance

Short-Term & Long-Term Disability

Employee Assistance Program

Job summary

Jubilant HollisterStier LLC in Spokane, WA is seeking a Validation Engineer II/III/Sr to provide pharmaceutical process validation knowledge and engineering activities across CDO, focusing on sterilization, lyophilization, aseptic processing, and related GMP systems. You will work with internal teams and external partners to improve processes and support regulatory compliance.

Responsibilities include developing specifications, RFQs, and project documentation, applying validation judgment, and

Qualifications

• Bachelor of Science in engineering (Mechanical, Chemical, Manufacturing, or similar).
• Experience in pharmaceutical validation and GMP operations.
• Knowledge of sterilization and lyophilization processes.

Responsibilities

• Provide technical support for CDO and engineering opportunities.
• Apply validation judgment to evaluate feasibility and requirements.
• Support regulatory compliance for facility, equipment and processes.
• Contribute to project management documentation and MS Project plans.
• Collaborate with internal/external stakeholders on technical initiatives.

Skills

Sterilization

Lyophilization

Aseptic processing

Mixing operations

Cleaning processes

Project Management

ISPE Baseline Guides

Regulatory compliance

Education

Bachelor of Science (Engineering)

Tools

MS Project

PowerPoint

Job description

Jubilant HollisterStier LLC in Spokane, WA is seeking a Validation Engineer II/III/Sr to provide pharmaceutical process validation knowledge and engineering activities across CDO, focusing on sterilization, lyophilization, aseptic processing, and related GMP systems. You will work with internal teams and external partners to improve processes and support regulatory compliance.

Responsibilities include developing specifications, RFQs, and project documentation, applying validation judgment, and