Factors Group of Nutritional Companies

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Closed listing

Factors Group of Nutritional Companies

Validation Coordinator

Coquitlam, BC, Canada

This opening has closed.

The original listing is kept below for reference.

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At a glance

Automatically prepared from the listing. Check the original description for the full requirements.

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Responsibilities

The Validation Coordinator will execute validation protocols for manufacturing and laboratory equipment while ensuring compliance with FDA, Health Canada, and GMP regulations. They will coordinate validation projects, maintain documentation, and collaborate with cross-functional teams to implement process improvements.

Requirements

Candidates must hold a Bachelor's degree in Chemistry or Engineering and possess at least 2 years of validation experience in a GMP pharmaceutical or dietary supplement environment. Proficiency in data integrity regulations and strong analytical laboratory skills are required.

Experience

2 to 5 years

Education

bachelor degree

Working hours

40 hours per week

Job type

Temporary
Full-time

Work arrangement

On-site

Skills

Validation protocols
IQ/OQ/PQ
GMP
21 CFR Part 11
Quality management systems
Data governance
Analytical laboratory skills
MS Office
Project coordination
Change control
Regulatory compliance
Technical documentation
Process improvement
Equipment maintenance
Risk assessment

Benefits

Healthcare
Health spending account
Personal spending account
Wellness days
Employee & Family Assistance Program
Safety boot voucher
Company provided PPE
Employee discount pricing
Employee appreciation events
Free onsite parking
Employee wellness sessions

Minimum pay

$57,000

Maximum pay

$71,500

Pay currency

CAD

Pay period

YEAR

Visa sponsorship

Not detected in the job text

Keywords

Validation
GMP
FDA
Health Canada
TGA
21 CFR Part 11
IQ
OQ
PQ
Quality Management
Data Governance
Data Integrity
ISPE Baseline Guide 5
Pharmaceutical
Dietary Supplement
Solid Dosage Forms
Change Control
SOP
Safety Policies
Engineering
Chemistry
Validation Master Plan
Corrective Action
Technical Writing
Compliance

Original job description

Archived listing. The details below describe a past opening.

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 will include the 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 and operate equipment 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; monitor progress of the validation master plan, procedures and strategies

Ensure validation efforts are conducted in an appropriate and timely manner

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 ensure timely completion

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 Degree in an appropriate science (Chemistry) or Engineering discipline
Validation experience or participation in validation work group activities (2+ years)

GMP industry experience in pharmaceutical or dietary supplement manufacture of solid dosage forms, in a hands-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)

You get:

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
Proudly Canadian owned & operated

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.

FGOffice

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