Moderna
(Fixed Term) Specialist, Validation (CQV)
Laval - Canada, CA · Senior · Full-time
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About the role
- B.S. in Chemical or Mechanical Engineering (or related discipline)
- Experience supporting deviation management and CAPA processes
Responsibilities
- Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
- Our mRNA vaccine manufacturing facility will support rapid access to respiratory vaccines produced domestically.
- Support validation of facilities, utilities, systems, and equipment across the site
- Execute requalification and periodic review activities to maintain compliance and validated state
- Collaborating with Manufacturing, Material Supply, Quality, Engineering, and QC to deliver validation activities aligned with project timelines and regulatory requirements
- Support deviation investigations, including root cause analysis and CAPA implementation
- Manage and complete quality records such as Change Controls, Deviations, and CAPAs related to validation activities
- Maintain up-to-date knowledge of regulatory expectations and industry best practices
- Support multiple systems, equipment, and validation projects simultaneously
Requirements
- The position requires proficiency in both French and English due to interactions with teams, partners, and tools located outside Quebec
- 4-7+ years of experience in CQV within a cGMP manufacturing environment
- Working knowledge of validation of facilities, utilities, systems, and equipment
- Support regulatory inspections and internal audits as required
Skills
- Strong technical writing and documentation skills
- Effective communication and collaboration skills
Company info
- By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture.
- Through local talent development and research collaboration, we are building a strong mRNA ecosystem in Canada.
Visa & Work Authorization
- As part of Moderna's commitment to build a sustainable workforce, a minimum of 2 years of work authorization is required for this role.
This listing is sourced directly from Moderna's careers page and normalized into a canonical job model.