Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it - where your skills and values drive our collective progress and impact.

Job Title Quality Control Reviewer

Department Quality Control

Reports To Title Supervisor, Quality Control

Supervise Direct Reports No

Shift

Permanent, Evening (15:30 - 24:00)

Introduction

We are looking for a trustworthy and respectful individual who consistently does the right thing. Someone who is imaginative and proactive, with a keen eye for what is possible. A perceptive and adaptive person who is action oriented. We need a disciplined, focused, and accountable team member. If you embody these values, come join our company and help us shape the future.

General Responsibilities

Provide support for the review and release of finished products/stability/in-process/raw material samples and instrument PM/calibration work orders to meet quality control schedules. Review of lab documentation, method validation documentation and procedures. Provide support with other duties as assigned by Supervisor.

Key Responsibilities

Participate in right the first-time quality control testing data review on various analytical techniques while following strict procedures/guidelines.

Collect, organize, and review scientific data thoroughly for site/contract lab within required timelines to ensure completion and accuracy and compliance with established procedures and standards by reviewing lab records and/or electronically for qualified instrument software. Make decisions regarding the acceptability of analytical data based on the documentation.

Perform periodic review of lab instrument/computerized systems as per defined procedure and intervals to enhance data integrity.





Perform review of data electronically through instruments software/LIMS and manually using lab records.

Assist in developing, writing, and reviewing and revising departmental SOP’s and Standard Test Methods. Assist with interpretation of USP and EP compendial requirements.

Review of analytical validation data. Review calibrations in the applicable database management.

Review out-of-specification laboratory investigations and provide support during audits and assist with the development and preparation of technical reports.

Provide guidance and feedback to lab personnel regarding compliance with positive documentation practices.

Ensure documents and records are meeting current data integrity and regulatory requirements and strictly followed as per defined procedures.

Ensure compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements in a manufacturing environment.

Working closely with Supervisor, provide strong technical support and daily coordination activities for lab.

Participate in the area of occupational health, safety, and wellness.

Education & Experience Requirements

Bachelor of Science degree with a major in Chemistry or College diploma in Chemical Technology

Minimum 3-5 years’ related industry experience for technical/scientific data review

Technical and Professional Requirements

Strong knowledge of US Pharmacopoeia (European Pharmacopoeia an assists).

Working knowledge of Health Canada, FDA, ICH regulations and guidelines that govern the pharmaceutical industry.





Thorough understanding/experience of analytical testing and laboratory instrumentation and their software (e.g. Empower, Lab-X, Chemstation)

Understanding of laboratory, computer software programs, including Microsoft Office, is required

Basic knowledge of statistical and trends

Strong knowledge of computer software programs (including Microsoft Office).

Core Competencies

Excellent communication, interpersonal and problem-solving skills

Self-motivated, positive attitude, attention to detail and a good team player

Able to work independently with tight deadlines

Strong analytical thinking and problem-solving skills

Good team player

Ability to manage multiple projects/tasks concurrently and effectively.

Excellent organizational and time management skills

Total Rewards The range of starting base pay for this role is $55,973- $75,000. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in our annual bonus program plan.

What we have to offer employees at our site:

Employee Assistance Program (EAP)

Employee Recognition Program

Full-service cafeteria with weekly lunch specials; free coffee and tea

Free energized parking

Free electric vehicle parking

Employee Stock Purchase Plan (ESPP) for qualifying employees

Registered Retirement Savings Plan (RRSP & DPSP) for qualifying employees

Free onsite gym

Years of Service Awards

Employee Referral Program

Maternity Leave top-up

Apprenticeship Leave top-up

We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

📌 Quality Control Reviewer (Lorette)
🏢 Bausch Health
📍 Lorette