Quality Control Technician at ZYUS Life Sciences
Saskatoon, SK, Canada -
Full Time


Start Date

Immediate

Expiry Date

05 Oct, 25

Salary

0.0

Posted On

05 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Record Keeping, Secondary Education, Analytical Instruments, Uv, Analytical Skills, Communication Skills, Regulatory Requirements

Industry

Pharmaceuticals

Description

QUALIFICATIONS:

  • Post secondary education in a relevant scientific field.
  • Previous experience in a quality control or laboratory environment preferred.
  • Experience with analytical instruments such as HPLC, UPLC, UV, etc.
  • Familiarity with regulatory requirements and quality standards (e.g., cGLP, cGMP).
  • Strong attention to detail and accuracy in record-keeping.
  • Excellent communication and teamwork skills.
  • Ability to work independently and collaboratively in a fast-paced environment.

SKILLS, KNOWLEDGE, AND ABILITIES:

  • Excellent written and verbal communication skills.
  • Excellent organizational and analytical skills with a high attention to detail.
  • Proficient in utilizing Microsoft Office applications.
    Must have the ability to maintain integrity and honesty at all times

How To Apply:

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Responsibilities

ROLE OVERVIEW:

The Quality Control (QC) Technician will be responsible for performing routine sampling and testing for product, raw material, and packaging, and equipment qualification in conformance with current Good Laboratory Practices (cGLP). They will conduct material sampling, maintain sample chain of custody, and report results accurately.

The following is a general description of duties that are done regularly in this role. Please note that employees will be asked to perform duties outside of the following to assist in other Company-related activities as required.

  • Conducting routine testing for product, raw material, and packaging.
  • Qualifying equipment in conformance with cGLP standards.
  • Maintaining sample chain of custody and reporting results accurately.
  • Performing material sampling and ensuring compliance with procedures.
  • Performing testing for analytical method development and validation.
  • Following established laboratory, regulatory, safety, and environmental procedures.
  • Adhering to cGLP standards and the company’s Quality Policies and site Standard Operating Procedures (SOPs).
  • Providing reports in a timely manner.
  • Collaborating with other lab personnel on projects.
  • Maintaining lab safety and orderliness.
  • Managing material and inventory control, including controlled substances.
  • Reporting and participating in resolving deviations and implementing CAPA
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