GMP Operations Lead: Process Improvement & Compliance

Jubilant Pharma Limited; Spokane (WA); On-site; USD 102,100 - 163,300; Full time

Benefits offered by this job

Medical, Dental & Vision coverage

FSA/HSA

Life & AD&D Insurance

Disability Insurance

Employee Assistance Program

Job summary

Jubilant Hollister Stier LLC in Spokane, WA seeks a qualified professional to lead and support cGMP manufacturing readiness, inspection processes, and cross‑functional initiatives. You will help develop inspection sets, qualification methods, and SOPs while coordinating with diverse teams to ensure compliant, validated manufacturing environments.

The role emphasizes project management, data analysis, and effective communication across levels of the organization, with a focus on continuous

Qualifications

• Bachelor’s degree in Engineering, Operations or Life Sciences, or 5+ years of related experience if no degree.
• Experience in project management and coordination.
• Strong analytical skills and proficiency in data analysis tools and techniques.
• Ability to communicate effectively to various audiences.
• Ability to influence across multiple levels and functions of the organization.

Responsibilities

• Provide SME on industry standards to enable integration of new products and processes.
• Develop and own inspection test sets and qualification processes.
• Coordinate cross-functional teams for GMP startup readiness and validation activities.
• Support manufacturing operations with projects that implement new technologies and improve processes.
• Lead continuous improvement initiatives including capacity optimization and cost reduction.

Skills

Project management

Communication

Analytical skills

Data analysis tools

Cross-functional collaboration

PPE compliance

Education

Bachelor’s degree in Engineering/Operations/Life Sciences

High School Diploma or equivalent

Job description

Jubilant Hollister Stier LLC in Spokane, WA seeks a qualified professional to lead and support cGMP manufacturing readiness, inspection processes, and cross‑functional initiatives. You will help develop inspection sets, qualification methods, and SOPs while coordinating with diverse teams to ensure compliant, validated manufacturing environments.

The role emphasizes project management, data analysis, and effective communication across levels of the organization, with a focus on continuous