Easter Seals Jobs

Description

Kenvue is currently recruiting for:
Supplier Quality Specialist

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.

Role reports to: Manager, Supplier Quality Management
Location: Skillman, NJ (Kenvue's corporate headquarters is currently located in Skillman NJ, but is scheduled to move to Summit, NJ in or around early 2025.)
Travel : 10%
Pay: $ 73,000 - 117,300

What you will do
The North America Supplier Quality Management team is seeking a Supplier Quality Specialist based in Summit, NJ (Ft. Washington, PA or Skillman, NJ until 2025).
This person will be responsible for training on applicable procedures and following the requirements for good documentation practices, GMP compliance, and Supplier Lifecycle Management for Chemicals or Packaging. They will work with their manager to ensure commitments are timely, accurate, and meet their intended objective. This employee will provide detailed and timely updates on the status of key projects and issues. The Specialist will exercise the highest level of integrity and communicate any deviations or compliance concerns to their manager promptly.

Supplier and/or Material Lifecycle Management, including:

Aid in the selection, onboarding, monitoring, and disengagement of new and existing suppliers or materials
Brings forward potential process improvements to manager to help drive compliance and/or efficiency

Regional Projects and Initiatives:
Participate in supplier engagements (Technical Assessments, FMEAs, Process Reliability, others); work as part of a cross-functional team, assess supplier current state, recommend improvements, document results, and partner with supplier to address action items
Engage with suppliers to drive remediation of open audit action plans
Develop and maintain collaborative partnerships to improve and sustain supplier/material reliability improvements

Non-Conformance Investigations, CAPA, Material Event Investigations
Support supplier or material non-conformance investigations to ensure robust supplier investigation and corrective actions meet Kenvue and regulatory expectations
Support your team and/or manager to understand and troubleshoot high-risk / high-complexity quality and compliance issues, using experience, ingenuity, and creativity to provide solutions to a wide range of root causes.

GMP Metrics and Data Management
Coordinate periodic reviews, data collection, and GMP evidence as vital for compliance requirements
Provide documentation and supplier data support during internal audits and regulatory inspections
Analysis across multiple data systems to assess material/supplier performance metrics and partner closely with Kenvue manufacturing sites to identify supplier/material issues impacting performance and develop supplier engagement strategies to improve performance
Using historical indicators, insights, and partnerships, implement proactive solutions to mitigate severity of, or prevent, the occurrence of material non-conformances or related events, at the local and regional scale

What we are looking for
Required Qualifications

Bachelor Degree or equivalent combination of education and experience is required
4 years experience in a technical function (Quality Assurance, Engineering, R&D) or Supply Chain function (Planning, Sourcing, Operations).
Experience working in a Pharmaceutical, Medical Device, or Consumer Health industry, or other highly regulated industries.
Demonstrated ability to collaborate as a team member with internal/external partners to enhance relationships and interactions, including interfacing with team members to inform, support proposed changes, and provide direct feedback.
Ability to value diverse perspectives and use that diversity to achieve results.
Ability to work with manager to prioritize a diverse workload, ensuring timelines and objectives are met.

Desired Qualifications
Experience with supplier audits and corrective action plans
Familiarity with root cause analysis, six sigma tools, or related methodologies
Familiarity with cGMP requirements and current FDA regulatory activity
Ability to analyze data and identify trends

What's in it for you
Annual base salary for new hires in this position ranges from $73,000 to $117,300 This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors.
Competitive Total Rewards Package
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Employee Resource Groups
This list could vary based on location/region

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...

Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity