Specialist, Validation

Overview

Join a Leader in Pharmaceutical Manufacturing — And Build What’s Next. Jubilant Hollister Stier LLC is Spokane’s largest manufacturing company and a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support life changing medicines around the world. We are nationally recognized for our expertise in producing sterile injectable vials and lyophilized products, and our Allergy business is a global leader in allergenic extracts that support treatments for allergies and asthma.

Jubilant Hollister Stier is proudly part of the global Jubilant Pharma family.

For the Builders, Innovators, and Doers — This Is Your Place. If you thrive on solving complex problems, improving systems, and building real solutions, you’ll feel at home here. Your ideas matter — and your impact is felt globally.

The Validation Specialist serves on project teams in support of complex capital, compliance, and contract projects while demonstrating expert technical validation expertise. The Validation Specialist also leads and assists in the execution and documentation of validation work to ensure critical production equipment meets satisfactory performance standards.

• Leads and executes equipment requalifications and performance qualifications on critical production equipment and other validation work as needed.
• Authors equipment requalification reports to provide documented evidence of equipment requalifications.
• Updates program and policy documents for requalification of new equipment. Authors SOPs for requalification of new equipment. Revises validation SOPs to ensure correct and up to date information and processes are followed.
• Demonstrates a working and theoretical knowledge of the operation of various equipment and systems such as lyophilizers, terminal sterilizers, tanks, autoclaves, dry heat ovens, rinsers, CIP and SIP systems, HVAC, aseptic processing areas, etc.
• Initiates deviations within the EQMS system. Assist with RCA and authors impact assessments. Completes minor deviations. Authors and approves change controls and CAPAs.
• Authors validation protocols and reports, developing validation strategies for validation projects.
• Demonstrates knowledge of validation principles and regulatory and industry standards and ensures their application in strategy and approach.
• Responsible for working interdepartmentally to ensure IQ/OQ/PQ of new equipment is complete.

Required:

• BS Degree (hard science)
• 3 years validation experience (1 year with MS Degree)
• Proficiency in standard business computer applications (i.e. Microsoft Outlook, Word, Excel, PowerPoint, etc.)
• Proficiency with EQMS, LMS, and EDMS
• Technical writing
• Mechanical aptitude

Preferred:

• Pharmaceutical and FDA regulated industry experience

• Ability to lift 50 lbs.
• Prolonged sitting, prolonged standing, exposure to allergens, working in confined spaces, working in aseptic areas, repetitive activity. Ability to work occasional evenings and weekends.

Spokane, WA — On Site

Weekday Days

Compensation & Benefits That Start on Day One — Because Your Well Being Matters. Hiring Wage: $84,300 – 134,900, with opportunities for growth, promotion, and annual raises.

Starting on your first day, you receive:

• Medical, Dental & Vision coverage
• Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
• Life & AD&D Insurance
• Short-Term & Long-Term Disability Insurance
• Employee Assistance Program

Jubilant Hollister Stier 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.

If you require assistance applying for a position, contact: J

Caring, Sharing, Growing — We are committed to enhancing value for customers and stakeholders by delivering innovative and economically efficient solutions, always with care for the environment and society.