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Validation Coordinator

Job in Coquitlam, BC, Canada
Listing for: Natural Factors Inc.
Full Time, Seasonal/Temporary position
Listed on 2026-09-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 57000 - 71500 CAD Yearly CAD 57000.00 71500.00 YEAR
Job Description & How to Apply Below

1550 United Blvd, Coquitlam, BC V3K 6Y2, Canada

Job Description

Posted Monday, August 10, 2026 at 10:00 AM

The Coordinator will perform validation activities for the processes, facilities, utilities, manufacturing, and laboratory equipment. Ensuring compliance with Health Canada/FDA/TGA regulations, Quality Management systems, Good Manufacturing Practices and 21 CFR Part 11 (Electronic Records and Signatures). Responsibilities willincludethe execution of validation protocols (IQ, OQ, PQ).

Temporary Full-Time (40 hours);
Contract until August 31, 2027

Monday to Friday 8:00 am – 4:30 pm (flexible)

$57,000 – $71,500

In this role, you will:
  • Maintain andoperateequipment in a safe and efficient manner
  • Coordinate with other functional departments to develop and implement validation test plans
  • Prioritize validation activities according to compliance and business needs
  • Coordinate projects and schedules;monitorprogress ofthe validation master plan,procedure sand strategies
  • Ensure validation efforts are conducted inan appropriateandtimelymanner
  • Interact with individuals from different disciplines (Production, Maintenance, Engineering, and Quality) to plan, execute and complete validation activities,including reports and corrective action items to ensuretimelycompletion
  • Oversee validation testing for new products and process improvements
  • Review all key documents developed and executed by applicable personnel
  • Maintain all validation documents
  • Participate in and review all change controls (CC) and evaluate for revalidation activities
  • Adhere to Safety Policies (SPs), Goods Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs)
You have:
  • Bachelors Degreeinanappropriate science(Chemistry) or Engineering discipline
  • Validation experience or participation in validation work group activities(2+ years)
  • GMP industry experience in pharmaceuticalor dietary supplement manufacture of solid dosage forms, in ahands‑on technical/analytical role
  • Good analytical laboratory skills
  • Ability to work with computers (specifically MS Office)
  • Knowledgeable about data governance and integrity regulations
  • Familiarity with ISPE Baseline Guide 5 (Second Edition) (an asset)
  • Great benefits (healthcare, health & personal spending accounts, wellness days, Employee & Family Assistance Program)
  • $200.00 safety boot voucher & company provided PPE
  • $300.00 per year to spend on company products
  • Employee discount pricing
  • Employee appreciation events & rewards
  • Free onsite parking
  • Employee wellness sessions
Why us?
  • We’re much bigger than you think, 30+ natural health brands loved across North America

This position is open to all qualified applicants who are legally entitled to work in the country in which this job is located. Only electronic applications can be accepted. This position will close when a competitive candidate pool has been identified. We thank you all for your applications and a member of our team will contact you soon. All the best!

All Internal applicants will be given priority for consideration for the first five business days that this position is posted. After that five days, Internal applicants will be considered along with all other applicants;however, areguaranteedat minimum a callfromthe

Talent

Acquisition team.

1550 United Blvd, Coquitlam, BC V3K 6Y2, Canada

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