revance
Quality Assurance Specialist
At a Glance
- Location
- Location
- Experience
- Up to 2 years
- Posted
- 2026-07-23T15:04:34-04:00
Key Requirements
Required Skills
Domain Knowledge
- Biotech
- Manufacturing
- Pharmaceutical
- Regulatory
Requirements
Basic understanding of cGMP and regulatory requirements for pharmaceutical production.
Responsibilities
Perform quality checks during manufacturing, filling, and packaging activities, including weight checks, seal integrity checks, line clearance verification, cleaning verification, and label reconciliation.
Document inspection activities in accordance with Good Documentation Practices (GDP) and company procedures.
Assist in the review of executed batch records for completeness and accuracy.
Support QA oversight of equipment set-up and clearance activities under supervision.
Follow established procedures to ensure compliance with 21 CFR Parts 210/211, ICH guidelines, and company Quality Management System (QMS) requirements.
Uphold GDP and data integrity standards during all inspection and documentation activities.