
About Revance
Transforming aesthetics with advanced biotechnology solutions
Key Highlights
- Headquartered in Nashville, Tennessee
- Over $500 million raised in funding
- Flagship product: DaxibotulinumtoxinA for aesthetics
- 251-1,000 employees focused on biotechnology
Revance Therapeutics, headquartered in Nashville, Tennessee, specializes in biotechnology with a focus on aesthetic and therapeutic products. Their flagship product, DaxibotulinumtoxinA, is a next-generation neuromodulator designed for both aesthetic and therapeutic applications. Revance has raised ...
🎁 Benefits
Revance offers competitive salaries, equity options, generous PTO, and a flexible remote work policy to support work-life balance....
🌟 Culture
Revance fosters a culture of innovation and scientific excellence, encouraging employees to contribute to groundbreaking advancements in biotechnology...
Overview
Revance is hiring a Senior Analyst in QC Analytical to provide technical expertise in analytical testing and instrumentation. You'll lead quality control activities in a cGMP environment, ensuring product quality and compliance. This role requires experience with various analytical techniques.
Job Description
Who you are
You are a Senior Analyst with extensive experience in analytical quality control, particularly in a biopharma manufacturing environment. You possess a deep understanding of complex analytical testing and instrumentation, and you are comfortable leading projects while mentoring junior team members. Your expertise in cGMP compliance ensures that all quality control activities meet regulatory standards. You thrive in a role that combines technical knowledge with leadership responsibilities, ensuring product quality and data integrity.
You have a strong background in performing and reviewing analytical tests for raw materials, in-process samples, and finished products. Your proficiency with techniques such as HPLC, UPLC, LCMS, ELISA, and CE-SDS allows you to troubleshoot complex issues effectively. You are detail-oriented and committed to maintaining high standards of documentation and compliance, authoring and reviewing GMP documentation, including SOPs and technical reports.
What you'll do
In this role, you will serve as a technical expert in analytical testing, leading quality control activities within a cGMP environment. You will perform and review complex analytical tests, ensuring that all results meet the required specifications. Your responsibilities will include authoring and approving GMP documentation, ensuring compliance with ICH, FDA, and EMA guidelines. You will act as a subject matter expert, troubleshooting equipment and method issues, and leading investigations into out-of-specification results using root cause analysis tools.
You will collaborate closely with cross-functional teams to ensure that all quality control activities align with organizational goals. Your leadership will guide the team in maintaining compliance and achieving high standards of product quality. You will also mentor junior analysts, providing guidance and support as they develop their skills in analytical testing and quality control processes.
What we offer
Revance offers a competitive salary range of $115k - $130k, plus bonuses, depending on experience and qualifications. You will work in a supportive environment that values your expertise and encourages professional growth. We are committed to fostering a culture of collaboration and innovation, where your contributions will have a direct impact on our mission to deliver high-quality biopharmaceutical products.
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