Assistant Scientist, Research & Development-12 month fixed term contract at Kenvue
Guelph, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

16 Nov, 25

Salary

0.0

Posted On

16 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

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.

Required Qualifications

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

How To Apply:

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Responsibilities

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
    What we are looking for

Required Qualifications

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