Quality Associate

1 day ago

Kelowna BC VX Y, Canada Supra Research Inc. Full time

Organizational Summary:

Supra Research Inc. (Supra) is a commercial laboratory accredited by CALA to ISO/IEC Supra provides third-party testing in a variety of markets including, but not limited to: Natural Health Products, Wine and Grapes & Cannabis.

Additionally, Supra performs contract Research and Development Work that may include anything from analytical method development to final product testing.

Job Summary:

The Quality Associate will be the secondary contact point, both internally and externally, for issues pertaining to Supra's accredited operations ( to include 17025, 17034 and 9001)

Additional responsibilities will include routine sample testing for clients as well as assisting in method development, writing of SOPS, and general laboratory duties as needed. This role requires a strong detail-oriented person with significant experience working in an ISO 17025 accredited environment and or similarly regulated environments.

Responsibilities

  • Assist Quality Manger in ensuring that the organization's Quality Management System (QMS) conforms to customer, internal, ISO/IEC 17025 and regulatory / legal requirements.
  • Manage the monitoring, measurement, and review of internal processes, including but not limited to: proficiency testing, control charting, corrective actions and internal audits.
  • Assist with the training of junior staff on the requirements of Supra's QMS.
  • Report to the management team on the performance of the QMS (example: results of quality audits, corrective actions) including the need for improvement.
  • Responsible for accuracy and timely inspection / calibration of monitoring and measuring devices.
  • Keep up on standards, regulations / laws and news, with respect to product (service) quality.
  • Responsible for routine review and updating of standard operating procedures (SOPs).
  • Plans and executes internal audits to facilitate continuous improvement.
  • Plans and executes method development and modification projects as needed.
  • Performs routine tests as needed.
  • Reports opinions and interpretations of data where necessary.
  • Follow and adhere to all given instructions including work procedures, Standard Operating Procedures(SOPs).
  • Strictly adhere to and observe all safety policies as outlined in the company policies and training sessions.
  • Other duties as assigned.

Requirements:

Technical

  • Bachelor's degree in a relevant degree in chemistry or related discipline.
  • Familiar with ISO/IEC 17025 requirements.
  • Minimum 2 years of laboratory experience in an ISO/IEC 17025 accredited facility or related industry experience.
  • Proficient with computer software, specifically Microsoft Excel, Word and ELNs.
  • Familiar with LIMS requirements.
  • Capable and willing to learning new software.
  • An equivalent combination of education and experience may be considered.

Attributes

  • Excellent communication in the English language, both written and verbal.
  • Ability to work independently as well as in a team environment.
  • Strong attention to detail and organizational skills.
  • Must be able to lift and move items up to 15kg.
  • Regular, predictable attendance is an essential function of this job.

Job Types: Full-time, Fixed term contract

Contract length: 12-18 months

Pay: $58,000.00-$62,000.00 per year

Benefits:

  • Casual dress
  • On-site parking

Work Location: In person

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