Scientist II Microbiology

Description

Kenvue is currently recruiting for:

Scientist II-Microbiology

This position reports to the Supervisor-Microbiology Lab and is based at Fort Washington PA

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: Supervisor-Microbiology Lab

Location: Fort Washington, PA

Travel %: none

What you will do

The Scientist II is responsible for providing testing, technical and troubleshooting support in the QC Laboratories

Key Responsibilities

• Collection, processing, method development and testing of chemical components, bulk products, raw materials, packaging components, finished products, marketed product stability, in-process 1materials, scale up, validation and cleaning validations to conform with specifications and standard operating procedures (SOPs).

• Thorough knowledge of SOPs, USP and other applicable pharmacopeia.

• Possess foresight to recognize task needs and performs the trained task without the request of management.

• Reviews and/or writes the following documents.

APR.

SOPs, QSRs, Instrument qualification, protocol/report writing, trending and review/analysis of data.

• Performs statistical analysis in support of APRs, Stability.

and Product Release.

• Complies with cGMPs, safety training and regulations.

• Performs more advance technical projects under the supervision of management.

Maintains an environment of respect and teamwork with all coworkers.

• Provide support during regulatory inspections/audits as directed.

Support may be in the form of scribes, runner and document gathering

• May provide statistical analysis in support of the APR and Stability processes

• Exposure to and working knowledge of electronic batch records and /or other automated processes/systems (labs)

• This role does require working 2-3 weekends per quarter and some holidays

What we are looking for

Required Qualifications

• Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required

• Minimum of 2 years of GMP/GLP quality control lab experience in a pharmaceutical and /or OTC and /or regulated environment is required

• Capable of performing r...