Sr. Scientist Technical Operations

Kenvue is currently recruiting for:

Sr. Scientist Technical Operations

This position reports to the Manager, Process Science and will be located in Fort Washington, PA or Skillman/Summit, NJ.

Who we are

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson’s and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to: Manager, Process Science

Location: Fort Washington, PA and Skillman, NJ; Kenvue is currently in the process of moving its Global Headquarters from Skillman, NJ to Summit, NJ.  This role is based in Summit, NJ but there may be a period of time during the transition that you must report to Skillman, NJ.

Travel Requirement: 25%, primarily North America

Pay: $73,000 - $117,300

What you will do 

As a member of the North America team in the Technical Operations (Process Science) department, this position provides technical support to commercial solid, liquid, and / or semi-solid pharmaceutical products, dietary supplements, new products in development, and technology transfer activities. You will engage in formulation and process development activities, characterization, process performance qualification, and continued process verification. Work is primarily focused on support of the External Manufacturing network for our Self Care OTC franchises.

The incumbent will ensure quality and compliance in all cGMP related activities, maintain all required training for the role, and follow standard operating procedures to complete the required work. Works with minimal direction. Influences internal and external cross-functional partners and stakeholders at multiple levels in the organization (such as Quality, R&D, and Supply Chain). Will maintain multiple projects at once.

Key Responsibilities:

• Design and complete experiments/deliverables at small and large/commercial scale to support project objectives that supports base business. Project tasks may include sample collection, in process testing, sample management, data analysis, etc.
• Prepare or approve technical memos or reports by analyzing data, developing conclusion