QA Specialist II (2nd Shift)

Description

Kenvue is currently recruiting for a:

QA Specialist II (2nd Shift)

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:
Manager Plant Quality

Location:
North America, United States, Pennsylvania, Lititz

Work Location:
Fully Onsite

What you will do

Performs product release on 2nd shift after completing record review and assuring that non-conformance investigations, laboratory investigations and quality systems are in compliance with the good manufacturing practices and good laboratory practices as established in the code of local government regulations and company procedures.

Provides QA support to operations.

Key Responsibilities


* Work with highly engaged and effective team.


* Perform quality review of production records including manufacturing, packaging, and laboratory documents.


* Responsible for releases of finished product based on conformance to established standards.


* Apply quality assurance processes, procedures, and activities.


* Conduct walkthroughs and assessments of GMP areas.


* Partner with Operations to address quality/compliance issues and improvements.


* Complete review of batch records for complaint investigations.


* Generate and distribute certificates of compliance to foreign affiliates.


* Review compliance records, specifications, procedures and other documents, as required by procedure.

Limited approval responsibilities.


* Generate, identify and suggest improvements as well as improvements to quality and plant operations.


* Participate in and lead process improvement teams as appropriate.


* Maintain ownership and train others on applicable SOP's.

Write and assist others is writing new or updated operating procedures.


* Conduct low risk/low complexity investigations and rationales which are technically accurate and regulatory compliance focused for all quality documentation including non-conformances, corrective actions, CAPAs and audit observation responses, quality reports, metrics.

QA management will provide support.


* Independent recommendations to Supervisor regarding com...