Quality Lead- External MFG, Nutritionals

Description

Kenvue is currently recruiting for:

Quality Lead - External MFG, Nutritionals

This position reports into External Manufacturing Quality Management and will be located in Skillman, 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: External Manufacturing Quality Management

Location: Draper, UT

Travel %: 10%

What you will do

The Quality Lead - External Manufacturing, Nutritionals position provides overall Quality Assurance Leadership in the management of contract manufacturing sites engaged in the production of oral ingestible and topical Dietary and Nutritional products for the Zarbee's Business Unit of Kenvue ensuring compliance to 21CFR111 and 21CFR117.

The external Manufacturing Quality Lead is responsible for supporting Contract Manufacturing sites, driving compliance & quality improvement initiatives, assisting resolution of process/product non-conformance events, monitoring/resolving complaints, reporting Contract Manufacturer performance metrics, interfacing with Zarbee's and Kenvue business partners and providing batch record release when required.

This position may represent QA on projects and improvement teams by guiding and setting quality/compliance requirements, development of SOPs & specifications, and providing technical transfer/validation support.

This individual will comply with Federal and worldwide regulations and meets the needs of the business and supply chain.


* Subject Matter Expert (SME) for quality assurance processes, procedures, and activities.

Remain current on assigned quality system training and seek out training and knowledge in adjacent areas.

A mentor to junior staff.


* Provides overview or detailed communications to Q&C and cross-functional leadership on status of key initiatives and issues.


* Document rationales which are technically accurate and regulatory compliance focused for product disposition, risk assessment/mitigation, non-conformances, corrective actions, and audit observation responses.

Hold business partners accountable for delivering documentation of similar quality.


* Conduct, execute and document thorough investigations and CAPAs for high risk/high comp...