Manager, Process Engineering

Revision Skincare® Where Skin Longevity Begins™

Revision Skincare® is a leading professional skincare company dedicated to advancing skin health through innovative, science-backed solutions. Our culture is built on curiosity, collaboration, and a passion for excellence. As part of our team, you'll work alongside talented professionals who are committed to research, innovation, and delivering measurable results for customers and healthcare professionals worldwide.

At Revision, we look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future.

The Manager, Process Engineering, will serve as Revision's technical lead for moving formulations from development into commercial-scale manufacturing, for maintaining the manufacturability of products already on the market, and tech transfer between CDMOs.

This role owns end-to-end technical transfers between CDMOs — including transfers of new products into initial manufacturing, and transfers of existing products from one CDMO to another — along with the scale-up activities, engineering and validation batches, and documentation required to bring each transfer to a successful, audit-ready close.

This individual will also lead process validation for OTC products in accordance with FDA monograph and cGMP requirements and will serve as the technical owner for assessing and managing the impact of raw material changes, substitutions, and supplier transitions on marketed products.

The Manager will work closely with Research & Clinical Development, Quality, Regulatory Affairs, Supply Chain, and our CDMO partners to ensure that every transfer, scale-up, and validation activity is executed on time, in compliance, and without disruption to product supply.

• Lead end-to-end technical transfer of formulations and manufacturing processes between CDMOs, including transfers of new products into first manufacture and transfers of established products from one CDMO to another.
• Serve as the primary technical point of contact for CDMO partners throughout transfer, scale-up, and commercialization activities.
• Develop and execute technical transfer protocols, risk assessments, and transfer plans consistent with ICH Q8/Q10 principles and Revision's quality standards.
• Coordinate engineering/qualification runs and GMP validation batches at receiving sites, and compile technical transfer reports documenting outcomes and any process adjustments.
• Support evaluation and qualification of new CDMO partners as needed for business continuity, cost optimization, or capacity expansion.

• Lead scale-up of formulations from lab/pilot scale to commercial manufacturing scale, identifying and resolving differences in equipment trains and critical process parameters.
• Partner with Formulation Science/R&D to translate bench-scale processes into robust, reproducible commercial manufacturing procedures.
• Troubleshoot manufacturing and process deviations that arise during pilot runs, scale-up, and commercial production.
• Apply process engineering principles — mixing, mass transfer, homogenization, emulsification, and similar unit operations — to optimize yield, consistency, and manufacturing efficiency.

• Lead process validation for OTC drug products in accordance with FDA OTC monograph…