The Senior Validation 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 will include the execution of validation protocols (IQ, OQ, PQ).
Temporary Full-Time (2-Year Contract)
Monday to Friday 8:00 am – 4:30 pm
In this role, you will:
Manage and review validation activities and projects to agreed project plans, timelines, and Validation Master Plan (VMP)
Balance multiple validation projects simultaneously to accomplish their completion efficiently and quickly
Provide accurate, neat, reliable, complete analysis reports, including result entry in computerized reports or Laboratory Information Management System, by following approved Work Procedures (WP) and Standard Operating Procedures (SOP), Analytical Methods (AM), and current Good Manufacturing Practices (cGMP)
Coordinate with other functional departments to plan, execute and complete validation activities including reports and corrective action items to ensure timely completion
Performance of a variety of validation activities including, but not limited to: Cleaning, Process, Content Uniformity, Equipment, Computer Systems, Method
Create and maintain process validation and cleaning matrice performance by equipment train
Use of company QMS systems for document creation, revision, review, approval, and retention
Support change control process through: initiation of change controls (CC) and document change requests (DCR), review of CC for validation impacts, performance of action items, and provision of additional data
Monitor activities, system performance, and compliance to VMP to contribute to monthly departmental key performance indicators (KPIs)
Mentor and develop more junior individuals
Lead and contribute to capital expenditure justification and submission, and subsequent project work
Travel to other sites (including out of country) for meetings and trainings as required
You have:
Bachelor’s degree in science (Chemistry) or Engineering discipline
Previous validation experience (3+ years)
GMP industry experience in pharmaceutical or dietary supplement manufacture of solid dosage forms (in a hands-on technical/analytical role)
Strong proficiency with MS Office and familiarity with LIMS
Valid BC driver’s license and access to a reliable vehicle
You get:
Great benefits (healthcare, health & personal spending accounts, 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
Why us?
We’re much bigger than you think, 30+ natural health brands loved across North America
Proudly Canadian owned & operated and a Certified B Corp company
Learn more about us here: https://ca.naturalfactors.com/pages/our-nature
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, are guaranteed at minimum a call from the Talent Acquisition team.
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