Assistant Scientist, Research
4 months ago
**Assistant Scientist, Research & Development-18 month contract**-2307011089W
Description
Kenvue is currently recruiting for:
**Assistant Scientist-Research and Development -**Contract role -**18 months**
This position reports into the analytical manager and is based in Guelph, Canada
**Who **W**e **A**re**
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.
**What **You Will Do**
Key Responsibilities:
Under limited supervision and in accordance with all applicable federal, provincial, and local laws/regulations, the Companies’ policies, procedures and guidelines, you will be responsible for:
- Performing assigned scientific experiments and routine tasks according to established procedures.
- Coordinating and/or executing: method validations and/or transfers; chemical and physical testing of stability samples; sampling and testing of process 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
You will also ensure quality and compliance in all actions by:
- Attending GMP training.
- Adhering to strict compliance with procedures.
- Exercising the highest level of integrity in the tasks performed.
- In a timely and prompt manner, identifying, reporting, and seeking correction for deviations noted in the workplace.
- Embracing a behavior of employee involvement and dedication to doing the job right the first time.
Qualifications
**What **W**e **A**re **L**ooking **F**or**
Required Qualifications
- Bachelor’s of Science Degree in related field
- 1-5 years experience within the pharmaceutical or related industry
- 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
- High familiarity with analytical instrumentation such as HPLC, UPLC, dissolution and electronic data systems such as Empower and LIMS (Laboratory Information Management System)
- Computer skills (ability to learn and use many different software packages)
**What’s **I**n **I**t **F**or** **Y**ou**
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More
- Learning & Development Opportunities
- Employee Resource Groups
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location NA-CA-Ontario-Guelph
Travel No
Job Function R&D
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