Revance · 1 day ago
QA Specialist – Manufacturing Quality Assurance
Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings. The QA Specialist I – Manufacturing Quality Assurance is responsible for providing on-the-floor support to ensure compliance with cGMP, SOPs, and regulatory requirements, while performing quality checks and assisting in batch record reviews.
BiotechnologyHealth CarePharmaceuticalTherapeutics
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
Participate in deviation documentation and investigations under the guidance of senior QA staff
Aid in the preparation and revision of SOPs and controlled documents
Perform other quality-related tasks as assigned by QA Management
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
Escalate potential compliance issues to senior QA staff in a timely manner
Support regulatory inspections and customer audits by providing accurate information as requested
Demonstrate proficiency in inspection methodologies, measurement tools, and acceptance sampling standards (e.g., ANSI/ASQ Z1.4)
Gain working knowledge of cGMP manufacturing and packaging operations
Learn and apply basic root cause analysis and problem-solving tools under the direction of senior QA personnel
Build proficiency in quality oversight practices and regulatory expectations through on-the-job training
Collaborate with operations staff to reinforce compliance and quality standards on the production floor
Participate in quality training sessions to support professional growth and readiness for Level II responsibilities
Qualification
Required
High School Diploma or equivalent required; Associate degree in a scientific or technical discipline preferred
Minimum 0–2 years of experience in Quality Assurance, Manufacturing, or a regulated industry (pharmaceutical/biotechnology preferred)
Basic understanding of cGMP and regulatory requirements for pharmaceutical production
Proficiency with Microsoft Office applications (Word, Excel, PowerPoint)
Strong attention to detail, communication, and organizational skills
Ability to follow procedures, take direction, and work collaboratively in a team environment
Benefits
Competitive Compensation including base salary and annual performance bonus
Paid time off, holidays, and floating holidays that can be used for whatever you choose
Generous healthcare benefits, Employer HSA match, 401k match, wellness discounts and much more
Company
Revance
We believe that science-powered innovation creates possibilities.
H1B Sponsorship
Revance has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (12)
2024 (16)
2023 (8)
2022 (10)
2021 (16)
2020 (3)
Funding
Current Stage
Public CompanyTotal Funding
$1.68BKey Investors
Athyrium Capital Management LPEssex Woodlands Healthcare PartnersMedicis Pharmaceutical
2024-08-12Acquired
2024-03-04Post Ipo Equity· $100M
2022-09-12Post Ipo Equity· $200M
Leadership Team
Recent News
MarketScreener
2025-10-27
Company data provided by crunchbase