Job Description

Quality Control Analyst - 12 Months Term

Job Location: Steinbach, Manitoba, CAN

Job Requisition ID: 15235

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 Analyst

Department : Quality Control Lab

Reports To Title : Quality Control Supervisor

Supervise Direct Reports : No

Shift : One Year Term, Sunrise (23:30 – 08:00)

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

Participate in routine sample testing such as raw materials, finished products, in-process, stability and cleaning validation using various laboratory instrumentation such as HPLC/UPLC and GC by strictly following established analytical procedures and/or compendia methods. The role contributes to right‑first‑time execution, compliance support, and continuous improvement initiatives. Provide support to other duties as assigned by Supervisor.

Key Responsibilities

• Participate in right the first-time quality control testing using various analytical instrumentation techniques while following strict procedures/guidelines.

• Perform Lab instruments day of use verification/calibration as per define procedure and identify and troubleshoot minor instrumental and analytical problems. Maintain Lab instruments in good working conditions.

• Maintain proper documentation of each task performed into applicable Lab books, worksheets or qualified software.

• Participate in revising of QC SOP’s and STM’s.

• Identify out-of-specification or out-of-trend results, report OOS/OOT results to Supervisor/Chemist ASAP and assist in the completion of lab investigation.

• Ensure compliance with good laboratory practices (GLP), good manufacturing practices (cGMP) and regulatory requirements.

• 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 of 2 years of experience in pharmaceutical or food industries.

Technical and Professional Requirements

• Hands-on experience on various analytical instruments.

• Strong understanding of Canadian and US cGMP requirements.

• Strong understanding of computer software programs, including Microsoft Office

Core Competencies

• Attention to details

• Excellent organizational and time management skills

• Analytical thinking

• Problem solving skills and attention to details

• Good team player

Total Rewards

The range of starting base pay for this role is $58,368 – $76,608. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location.

What we have to offer employees at our site:

• Health insurance commences upon start date
• 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
• Free onsite gym

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.