EXTE RN/Registered Nurse AL MFG QUALITY SPECIALIST 1

External Mfg Quality Specialist 1 - 240#W

• Description
•

Kenvue is currently recruiting for:

• External Manufacturing Quality Specialist I
•

This position reports into the External Manufacturing Quality Manager and will be located at 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, were the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnsons 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 futureand yours. For more information, click here ( .

• Role reports to:
• External Manufacturing Quality Manager

• Location:
• Skillman, NJ _Kenvues corporate headquarters is currently located in Skillman NJ, but is scheduled to move to Summit, NJ in or around early 2025._

• Travel %:
• 10%, primarily North America

• Pay
• : $50,000 - $80,500

• What you will do
•

The External Manufacturing (EMQ) Specialist I position provides overall Quality Assurance support in the management of contract manufacturing sites engaged in the production of oral ingestible and topical OTC drugs, medical devices, combination products, nutritionals, NDAs and/or cosmetic formulations for the J&J Consumer Sector. This position is providing support to the Make Q&C External Manufacturing Quality (EMQ) department and EMQ Leads to manage and maintain trackers and/or databases, assess and facilitate release of product at external sites and in SAP, revise procedures and approve specifications and/or other similar tasks, as well as support and lead quality projects and compliance initiatives.

Key Responsibilities

+ Maintaining and improving trackers and/or databases to monitor quality metrics and data

+ Supporting the collection and coordination of quality documentation and records for product approval

+ Working with the internal quality team to support activities with internal and external suppliers and manufacturers on quality related issues, including management of event notification to EM network

+ Releasing of acceptable product in quality systems (e.g. SAP, Epicor) based on record review

+ Managing SOP creation, revision, and obsolescence processes in electronic management systems, as well as reviewing and approving of specifications

+ Maintaining quality records: Quality Agreements, Excelence Through Quality (ETQ) NextGen activities, etc.

+ Acting as a training administrator and supporting on-boarding and on-the-job training process, as well as maintaining training reports for EMQ team

+ Supporting recognition program and providing metrics/reports on its utilization and submissions.

+ Executing activities for global change controls and New Product Introduction projects, which includes but is not limited to first article inspections, SAP verifications, specification approvals and document reviews.

+ With a modest amount of daily direction and oversight from manager, prioritizing highly complex and diverse workload ensuring deliverables are on-time, accurate, and meet their intended objective.

• Qualifications
•

• What We Are Looking For
•

Required Qualifications

+ A minimum of a Bachelor's Degree or higher, or in the final stages of obtaining such (Q1-Q2 2022 Graduate).

+ Detail-oriented, with the ability to work in a fast-paced environment with multiple, concurrent priorities, many needing immediate resolution

+ Strong communication (verbal & written) and interpersonal skills, self-awareness and adaptability required.

+ Collaborative and successful at establishing relationships with internal and external partners

+ Demonstrated ability to work on complex or ambiguous issues autonomously, with little/no daily direction

+ Experience in MS Word, Excel, and Power Point applications

+ Travel Requirement: 0-10%

Desired Qualifications

+ A focused degree in Engineering, Chemistry, Biology, Biological Sciences, or Information Management

+ 0-2 years of work experience in GMP environment.

+ Experience with SAP and Excelence Through Quality (ETQ)

• Whats in it for you
•

+ Competitive Total Rewards Package

• + Paid Company Holidays, Paid Vacation, Volunteer Time & More!

+ Learning & Development Opportunities

+ Employee Resource Groups

• Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

#vdh

• Primary Location
• NA-US-New Jersey-Skillman

• Other Locations
• NA-CA-Ontario-Guelph

• Job Function
• Quality Assurance

• Req ID:
• 240#W