G.W. Seier founded Vita Health Products in Winnipeg, Manitoba in 1936. Since then, the company has grown from a small mail-order operation selling herbs and patented medicines into one of Canada's foremost suppliers of over the counter (OTC) pharmaceutical products and natural health products.

Based in Winnipeg – the geographic centre of Canada – and located in the St. Boniface industrial park, IVC Vita Health Products is a vertically integrated manufacturer, marketer, and distributor of a broad line of high-quality, nutritional supplements, and over the counter medications throughout Canada, with over 260,000 square feet of manufacturing, packaging, and distribution facilities.

IVC Vita Health has a long and proven track record of success and continues to demonstrate strong results with consistent growth. IVC Vita Health is part of the IVC Nutrition Corporation of Companies.

Join us at IVC Vita Health and be part of a team that values your contributions and invests in your success. We are committed to creating a workplace where diversity is celebrated, and every team member can thrive both personally and professionally.

Our Vision: The Canadian partner driving self-care innovation to enrich health.

Summary:

The Validation Student will support the Validation Department in executing and maintaining validation and calibration activities related to equipment, processes, facility, utility, and cleaning procedures. This role is ideal for a student or recent graduate in a science or engineering discipline looking to gain hands-on experience in a regulated pharmaceutical environment.

Responsibilities:

• Assist in the preparation and execution of validation protocols (IQ/OQ/PQ).
• Support equipment, facility, utility, and cleaning validation and verification activities.
• Participate in the review and maintenance of validation documentation.
• Collect, compile, and analyze data from validation tests and studies.
• Assist with the organization and filing of validation records.
• Assist with preparation of transport study reports
• Support in maintaining calibration records and scheduling.
• Work collaboratively with other departments such as Quality Assurance, Production, and Maintenance.
• Perform other duties as assigned by the Validation Supervisor.

Experience:

• Previous experience in a GMP or regulated setting is an asset but not required.
• Strong interest in validation, quality systems, and regulated manufacturing environments preferred.

Education, Certification, Licenses, & Registrations:

• University Degree or College Diploma (completed or in progress) in Engineering, Chemistry, Microbiology, Biochemistry, or related sciences,

Skills:

• Good technical writing and organizational skills.
• Ability to follow written procedures and work instructions.
• Detail-oriented with strong analytical and problem-solving skills.
• Proficient in Microsoft Office (Word, Excel, Outlook).
• Able to work independently and within a team environment.

Physical Demands:

• Standard office and lab environment.
• May include occasional lifting of lab materials (up to 25 lbs).

Vita Health Products Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, national or ethnic origin, colour, religion, age, sex, sexual orientation, marital status, family status, disability and conviction for an offence for which a pardon has been granted or in respect of which a record suspension has been ordered.

Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job

at any time. Additionally, this job description reflects management's assignment of essential functions, it does not

prescribe or restrict the tasks that may be assigned.