Microbiology Supervisor

Kenvue•Fort Washington, PA

6d•Onsite

About The Position

Kenvue is currently recruiting for a Microbiology Supervisor. 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. 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.

Requirements

Bachelors Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology or related science is required
Minimum 4 years of GMP quality lab experience
Experience in Microbiology

Nice To Haves

Prior Supervisory experience is preferred

Responsibilities

Leads and oversees all laboratory personnel, ensuring effective daily operations and serving as the designee for the Microbiology Manager in their absence.
Responsible for the final review and approval of microbiological testing across a wide range of activities, including components, raw materials, in‑process and bulk materials, finished products, commercial stability, method transfer, method development and qualification, and cleaning validation.
Ensures that all data is generated, reviewed, and released with the highest standards of technical rigor, compliance, and efficiency.
Works closely with internal stakeholders and external partners to support manufacturing, product release, stability programs, development initiatives, and validation activities.
Provides technical support and trouble-shooting for technical issues internally and externally.
Authors, reviews and leads lab investigations.
Reviews and/or writes the following documents: APR, SOPs, QSRs, Instrument qualification, protocol/report writing, trending and analysis of data, and laboratory investigations.
Ensures compliance with cGMP's and safety training and regulations.
Maintains an environment of respect and teamwork with all coworkers.
Acts as technical advisor for testing issues.
Interacts with regulatory agencies as required.