North AmericaFull TimeEngineering
Remotely
quality systemsregulatoryprocess developmentgmpcgmpbiologicsrisk based
Job Description
📋 Description
- Provide cross-functional Product Quality leadership for late-stage and commercial biologics
- Develop, implement, and manage quality strategies aligned with product development, manufacturing
- Lead and support activities related to annual product reviews, specifications, comparability
- Author and review GMP and regulatory documentation, including Product Quality-owned sections of
- Evaluate complex process and product-quality data using science- and risk-based approaches to
- Support investigations, change controls, product quality risk assessments, and other lifecycle
🎯 Requirements
- Hold a Doctorate degree with 2+ years of relevant Quality, Operations, Scientific, or Manufacturing
- Preferably hold a B.S. or advanced degree in Chemistry, Biochemistry, Biology, Pharmaceutical
- Bring experience of increasing responsibility within quality, analytical development, process
- Demonstrate 6+ years of experience working in a regulated environment, including direct GMP or
- Have experience authoring or reviewing regulatory documentation such as market applications, INDs
- Demonstrate strong knowledge of cGMP requirements and international regulatory expectations.
🎁 Benefits
- Comprehensive health and welfare benefits for eligible employees and dependents.
- Medical, dental, and vision coverage.
- Retirement and savings plans with employer contributions.
- Life and disability insurance.
- Flexible spending account options.
- Eligibility for a discretionary annual bonus program.
Back to all jobs