Scientist, Research & Development-12 month fixed term contract

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. For more information, click here.

Role reports to:

MANAGER ANALYTICAL

Location:

North America, Canada, Ontario, Guelph

Work Location:

Fully Onsite

What you will do

The 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:

• Leading the execution of analytical requirements for R&D projects
• Participate on cross-functional project task forces and support the development of project timelines
• Coordinate all aspects of the analytical project including method transfer and stability studies
• Coordinate the preparation of protocols, testing, and final reports
• Performing assigned scientific experiments and routine tasks according to established procedures.
• Conduct and review laboratory investigations.
• Reviewing data and documents.
• Keeping accurate records and supporting the development of technical documentation.

What we are looking for

Required Qualifications

• Minimum B. Sc.
• Minimum 3-5 years’ experience within the pharmaceutical or related industry
• Strong oral and written communication
• Demonstrated good problem solving and decision-making skills
• Creativity and innovation skills
• Collaboration and organizational skills
• Good documentation practices.
• Strong digital literacy
• 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.