Process Scientist (MS&T)- Material Management

Description

Kenvue is currently recruiting for:

Process Scientist (Manufacturing Science & Technology)- Material Management.

This position reports to the Tech-Ops cluster lead - EMEA Self Care and is based at Prague (CZ).

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® that you already know and love.

Science is our passion; care is our talent.

Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.

With expertise and empathy, being a Kenvuer means to have the power to impact 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 .

What you will do

The Process Scientist - Materials Management is responsible for driving and executing Technical Operations projects related to the qualification of alternative raw and packaging materials for the Kenvue marketed OTC products.

Key Responsibilities

• As part of OTC products lifecycle management, drive technical operations-owned activities related to the qualification of alternative API, raw materials & primary packaging.

• Prepare and submit for approval the validation strategies for assigned projects, partner with the manufacturing site and local validation teams to plan and execute the validation activities; prepare and/or review validation protocols and reports as well as related documentation.

• Ensure adequate risk management within the validation strategy.

• Present proposed material validation strategies and outcomes and gather approval by independent expert's panel.

• Provide process science /validation expertise in troubleshooting to resolve manufacturing/formulation issues.

• Proactively identify and drive process and cost improvement when feasible.

• Perform statistical analysis of technical data.

• Ensure adequate documentation is available to support registration of projects.

• Ensure appropriate and timely communication to relevant stakeholders

What we are looking for

Required Qualifications

• Bachelor or Master of Science within a relevant chemistry or pharmaceutical area

• 3 years of experience in process and drug product development, drug product manufacturing or related areas within the pharmaceutical/OTC industry and technical knowledge is essential

• Broad knowledge of pharmaceutical dosage forms (e.g.

solid dosage forms, liquids and/or creams)

• Broad knowledge of validation requirements, especially process and packaging validation

• Risk management experience

• Excellent technical writing skills

• Strong leadership skills and t...