Quality Scientist I- Reviewer- 12 Months

Description

Kenvue is currently recruiting for:
**Quality Scientist I - Reviewer - 12 months**

This position reports to Quality Laboratory Supervisor and is based at Guelph, Canada.

This position resides on **Weekend Shift **(Friday-Saturday-Sunday-Monday; 7:00 am-5:00 pm or 8am-6pm).

**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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the 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.

**Role reports to**:Quality Laboratory Supervisor

**Location**:Guelph, Ontario, CANADA

**Travel %**: 0

**What you will do**

As a member of the Analytical Quality Laboratory team, the **Quality Scientist I - Reviewer (Weekend Shift - 1 Year Contract)** will review all documentation related to the chemical quality testing of raw materials, packaging components, bulk work in process, and finished products. The Quality Scientist I - Reviewer will ensure compliance with Kenvue Corporate policies, internal requirements and Regulatory requirements.

They are responsible for the review of finished products in the continuing stability program to ensure formulations are stable throughout their shelf life.

The Quality Scientist I - Reviewer will work with business partners to identify and implement continuous improvement projects and support the investigation of quality events. This position offers ample opportunity for career growth and independence.

**Key Responsibilities**
- Review and approve lab documentation in various systems, and hardcopy worksheets/logbooks
- Independently generate reports (LIRs, Near Miss/Accident Reports, Change Controls) as required
- Identify non-value added activities and own the implementation of innovative approaches to continuously improve current systems and processes in order to maximize business results
- Identify risks within the laboratory and raise as appropriate
- Support team activities to ensure completion in a timely and compliant manner according to written procedures
- Ensure self and others are adhering to GMP and GDP requirements
- Provide frequent feedback to peers and others to ensure high quality documentation
- Provide training/share expertise with colleagues to ensure quality processes are followed
- Ensure that testing and reporting of results meets the needs of the business and regulatory requirements, and ensure compliance with internal specifications, regulatory and corporate policies
- Lead in a team environment through open communication and demonstration of values consistent with the Kenvue values and Leadership Behaviours: Lead, Deliver, Shape & Connect
- Follow Kenvue policies, quality/technical standards, health, safety, and environmental regulations, and regulatory requirements (Health Canada, United States FDA etc.)

Qualifications

**What we are looking for**

Required Qualifications
- Minimum of Bachelor’s Degree in chemistry or a related field, or equivalent experience within the pharmaceutical industry
- Minimum of 2 - 3 years experience in a Quality, or R&D environment in the pharmaceutical, food or water industries
- Good knowledge of GMP regulations
- Strong digital literacy

Desired Qualifications
- Ability to work with limited supervision and function optimally in a team environment is essential
- Good interpersonal and collaboration skills
- Excellent communication skills
- Demonstrated ability to organize, multitask and prioritize workload
- Good technical writing and problem-solving skills
- Excellent attention to detail
- Familiarity with computer software and strong personal computer skills
- Enjoys working to multiple timelines in a dynamic and fast-paced team environment
- Familiarity with USP guidance and guidelines is an asset
- Knowledge of Process Excellence/Lean is an asset

**What’s in it for you**
- Competitive Total Rewards Package*
- Paid Company Holidays, Paid Vacation, Volunteer Time & More
- Learning & Development Opportunities
- Employee Resource Groups
- This list could vary based on location/region
- Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qu