Job Description

Kenvue is currently recruiting for a:


Assistant Scientist, Research & Development-12 month fixed term contract

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.

Role reports to:

MANAGER ANALYTICAL

Location:

North America, Canada, Ontario, Guelph

Work Location:

Fully Onsite

What you will do

The Assistant Scientist provides analytical support to the growth and strategic business objectives of Kenvue with focus on North American supply chain initiatives.

Key Responsibilities

Under limited supervision and in accordance with all applicable federal, provincial, and local laws/regulations, the Company's policies, procedures and guidelines, you will be responsible for: Performing assigned scientific experiments and routine tasks according to established procedures. Executing method validations and/or transfers; chemical and physical testing of stability samples; sampling and testing of developmental and/or validation batches. Assisting in laboratory investigations. Collating, analyzing, and processing data. Reviewing data and documents. Keeping accurate records and supporting the development of technical documentation. Developing cross-functional understanding and awareness through exposure to diverse projects, products, and teams. Operating current laboratory instrumentation and adhering to laboratory safety, SOPs and GMP/GLP regulations. Recommending minor modifications to existing systems, processes, techniques, or programs for improvement. Actively participating in project team meetings

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Required Qualifications

Minimum Bachelor of Science degree 1-5 years experience within the pharmaceutical or related industry High familiarity with
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HPLC

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UPLC

Dissolution

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Electronic data systems (Empower, LIMS)

Strong digital literacy Strong oral and written communication Good problem solving and decision-making skills Understanding of Good Manufacturing Processes, Good Laboratory Practices, Good Documentation Practices General knowledge of the pharmaceutical industry
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.