Revance

About Revance

Transforming aesthetics with advanced biotechnology solutions

🏢 Tech, Biotechnology👥 251-1K📅 Founded 2002📍 Nashville, Tennessee, United States

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 Quality Engineer, Validations to lead validation activities for complex manufacturing systems in a regulated environment. You'll serve as a technical leader and mentor junior engineers. This role requires extensive experience in quality engineering.

Job Description

Who you are

You are an experienced Senior Quality Engineer with a strong background in validations and qualifications in a cGMP environment. You have a proven track record of leading validation lifecycle activities, including process validation and equipment qualification, ensuring compliance with regulatory standards. Your expertise as a Subject Matter Expert (SME) allows you to provide technical guidance and problem-solving support to cross-functional teams, including Engineering, Manufacturing, and Quality. You have excellent communication skills and enjoy mentoring junior engineers, contributing to the development of site-wide validation standards and best practices.

You thrive in a collaborative environment, where you can drive validation strategies and ensure alignment with business requirements. Your experience includes authoring and executing Installation, Operation, and Performance Qualification protocols for complex systems, utilizing a risk-based approach to decision-making. You are detail-oriented and understand the importance of maintaining continuous compliance across manufacturing processes.

What you'll do

In this role, you will lead and execute validation and qualification activities for complex manufacturing systems, equipment, and processes. You will be responsible for authoring, reviewing, and approving qualification protocols, ensuring they meet regulatory and business requirements. As a Validation SME, you will provide technical guidance to various teams, helping to resolve issues and improve processes. You will also play a key role in project planning and risk assessment, contributing to the overall success of validation strategies.

You will mentor junior engineers, sharing your knowledge and expertise to help them grow in their roles. Your contributions will be vital in establishing best practices for validation across the site, ensuring that all activities align with regulatory compliance. You will collaborate closely with cross-functional teams to support lifecycle validation strategies and development-to-commercial transfers, making a significant impact on the quality and reliability of manufacturing processes.

What we offer

Revance offers a full-time position with flexible PTO and a bonus structure. You will be part of a dynamic team that values collaboration and continuous improvement. We encourage you to apply even if your experience doesn't match every requirement, as we believe in fostering a diverse and inclusive workplace.

Interested in this role?

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