Revance · 5 hours ago
Sr. Analyst, QC Analytical
Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings. The Senior Lead Analyst in Analytical Quality Control serves as a technical expert in complex analytical testing and instrumentation, providing leadership and project management for quality control activities within a cGMP environment.
BiotechnologyHealth CarePharmaceuticalTherapeutics
Responsibilities
Analytical Testing: Performing and reviewing complex analytical tests for raw materials, in-process samples, and finished products using techniques such as HPLC, UPLC, LCMS, ELISA, CE-SDS, and various compendial methods
Documentation and Compliance: Authoring, reviewing, and approving GMP documentation, including SOPs, test methods, protocols, technical reports, and quality records (deviations, OOS, CAPAs, Change Controls). Ensuring all activities adhere to cGMP and GLP. ICH, FDA, and EMA guidelines
Troubleshooting and investigation: Acting as a subject matter expert (SME) to troubleshoot complex equipment and method issues, and leading thorough investigations into out-of-specification (OOS) or out-of-trend (OOT) results using root cause analysis tools
Method Lifecycle Management: Leading and supporting the development, optimization, transfer, qualification, and validation of analytical methods for new and existing products
Leadership and Training: Mentoring and training junior analysts, guiding staff in laboratory procedures, and potentially managing day-to-day team activities and resource allocation
Project and Cross-Functional Collaboration: Leading projects and collaborating with cross-functional teams such as Manufacturing, Quality Assurance, Regulatory, and Analytical Development to meet deliverables and support regulatory inspections
Qualification
Required
Bachelor of Science in Biochemistry, or a related pharmaceutical biotechnology discipline
8+ years in a Quality Control laboratory, specifically within a cGMP biopharmaceutical or pharmaceutical environment for a commercially approved product
Must have extensive hands-on experience with relevant analytical instrumentation and software (e.g., Empower, SoftMax, LIMS)
Must be detail-oriented and have experience in formal technical writing for Quality Control laboratories (e.g., SOPs, Quality Records, Method Validation/Transfer Protocols, Method Validation/Transfer Reports)
Must have extensive experience in peer-reviewing of Quality Control data
Experience with the management of stability studies, stability data analysis, and stability data report generation
Experience in scheduling of Quality Control analytical testing for a team of analysts with throughput time adherence
Experience with CMO support for external operational management
Must have experience in Lean Six Sigma methodologies for bottleneck reductions and high throughput efficiencies in a commercial manufacturing environment
Preferred
Master of Science in Biochemistry, or a related pharmaceutical biotechnology discipline
Effective written and verbal communication skills
Lean Six Sigma Black Belt or PMP experience using Lean methodologies for process improvement
Critical reagent management experience (procurement, preparation, qualification, and management of inventory) is preferred
Raw Material management experience in sampling, qualification, and management of testing activities
Benefits
Competitive Compensation, including base salary and annual performance bonus.
Flexible PTO, holidays, and parental leave.
Generous healthcare benefits, HSA match, 401k match, employer-paid life and disability insurance, pet insurance, 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