Quality Analyst 1, Stability

What we do

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® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are 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 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:

Quality Stability Manager

Location:

North America, United States, Pennsylvania, Fort Washington

Work Location:

Hybrid

What you will do

The Quality Analyst I will contribute to the Consumer North America Quality Systems processes for Stability functions. You will work with a team of professionals all operating towards the goals and expectations of Kenvue, the new consumer company. You will support the team to help with cross functional Compliance & Quality improvement initiatives within the Stability programs. You will provide support for APR and MPS Stability group for Consumer and Self-Care. Success is measured through outcomes and performance metrics related to the processes.

Key Responsibilities

• Oversee NA External Manufacturing Stability program for Consumer Source Quality and Self-care products.
• Provide Quality Assurance expertise in management of stability studies at External Manufacturing and Contract Laboratories
• Review externally generated Stability data/CoAs/protocols for accuracy and completeness.
• Review and assemble Annual Stability Reports in support of ADPR/APR as required.
• Interface with Kenvue business partners and participate in cross-functional teams representing the EM Stability group.
• Maintain up to date knowledge of industry practices and compliance.
• Adhere to strict compliance with procedures applicable to the role.
• Exercise the highest level of integrity in the tasks performed.

What we are looking for

Required Qualifications

• Bachelor’s Degree in a technical field (Chemistry, Engineering, Sciences, Pharmacy or similar disciplines) required.
• A minimum of 1 years of professional experience in a regulated industry is required (Pharmaceutical, OTC Drug, Cosmetic, and/or Food and Dietary Supplements Industry).

Desired Qualifications

• Detailed working knowledge of cGMP requirements
• Proficient in Microsoft Office applications
• Knowledge of 21 CFR 210 & 211 and ICH guidance.
• Strong communication (verbal, written, and presentation) and interpersonal skills, self-awareness and adaptability required.
• Theoretical and/or hands experience in applied analytical chemistry and related instrumentation such liquid and gas chromatography, FTIR/UV/Vis/NIR spectrometry and wet chemistry.
• Experience in a Quality support function.

What’s in it for you

$61,880.00 - $87,360.00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

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