ABOUT US

Our Company’s name Viva Pharmaceutical Inc. Since its inception in April 1994, Viva Pharmaceutical Inc. has built a reputation as a leading manufacturer committed to the production of custom-made pharmaceutical and natural health food products for its customers worldwide.
Viva Pharmaceutical Inc. creates natural products and ingredients aimed at helping consumers get and stay healthy. Those products are offered in a variety of popular forms – including softgel and hard-shell capsules, as well as traditional tablets. The company also offers custom manufacturing, private labeling, and testing services for retailers, resellers and manufacturers.

PREFERRED QUALIFICATIONS AND/OR EXPERIENCES:

• An appropriate combination of post-secondary education in an applicable discipline of science (chemistry, biochemistry, biology or related) or specific medical training (pharmacology, pharmacokinetics, nutritional research or related).
• Two or more years of experience in the pharmaceutical/nutraceutical related industry.
• Advanced knowledge/understanding of GMP and FDA guidelines for manufacturing/packaging of pharmaceutical/nutraceutical products.
• Excellent verbal/written communication skills
  Job Types: Full-time, Permanent
  Pay: $42,000.00-$45,000.00 per year

Benefits:

• Casual dress
• Company events
• Dental care
• Extended health care
• Life insurance
• On-site parking
• Vision care

Flexible language requirement:

• French not required

Schedule:

• 8 hour shift
• Monday to Friday
• Night shift

Ability to commute/relocate:

• Richmond, BC V6V 1K8: reliably commute or plan to relocate before starting work (required)

Application question(s):

• Are you legally entitled to work in Canada?
• What are your salary expectations?

Education:

• Bachelor’s Degree (required)

Experience:

• Quality Assurance: 1 year (required)

Work Location: In person
Expected start date: 2025-07-1

• Perform routine sampling in support of the Quality Control Department.
• Maintain and update Batch Records according to the company working standards.
• Perform routine calibration on scale, balance, and instruments.
• Perform routine checks following the working procedures in the production area.
• Review packaging SOI printing technical documents as directed.
• Coordinate with other departments on QC related issues.
• Review analytical/associated data/records to support qualification and validation activities.
• Routine equipment calibration and quality check of in-process controls.
• Perform various quality checks for HST, SGC, INS and PKG.
• Review documentation and log entries for completeness and accuracy.
• Become familiar with GMP regulations, SOPs and safety requirements.
• Perform other duties assigned by senior staff.
• Work on environmental reports; air, water, data loggers, Surface and Personnel.
• Perform Line Clearance on all the operation before operations starts.