ABOUT US

At ABK Biomedical, based in Halifax, Nova Scotia, we’re transforming interventional radiology through the development of proprietary embolization technologies that enhance the treatment of hypervascular tumors and improve patient outcomes.

QC LABORATORY ANALYST

ABK Biomedical is looking for a motivated QC Laboratory Analyst to join our Quality Lab team. This role will report to the Director, Quality Assurance and will be responsible for applying general technical knowledge and skills to perform routine laboratory analyses and monitor basic laboratory equipment and inventory. The QC Laboratory Analyst will support the day-to-day manufacturing and inspection activities of products and R&D activities at ABK Biomedical, in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

KEY QUALIFICATIONS, SKILLS & EXPERIENCE

• Post-secondary education in a relevant field such as Medical Laboratory Technology, Biomaterials, or Chemistry.
• 1+ years’ experience in a similar role.
• Proficient in the use of analytical test equipment.
• Routine testing of materials experience.
• Strong capability to perform technical/analytical testing procedures.
• Strong aptitude for computer controlled analytical test equipment.
• Critical thinker with an aptitude for troubleshooting/process improvement.
• Strong documentation skills and attention to detail.
• Strong communication skills.
• Skilled in standard Office applications like Word and Excel.
• The ability to work cohesively with a cross-functional team in a fast-paced environment.
  We thank all applicants for their interest; however, only those selected for an interview will be contacted.
  ABK Biomedical is an equal opportunity employer and accommodates people with disabilities throughout the recruitment and selection process.
  Job Types: Full-time, Permanent
  Pay: $45,000.00-$65,000.00 per year
  Work Location: In perso

• Perform release testing on finished products to ensure they meet specifications.
• Perform materials characterization and in-process testing on raw materials and in-process products.
• Document test results and complete required Device History Record (DHR) documentation in a timely manner, adhering to Good Documentation Practices (GDP).
• Manage Maintenance and Calibration activities for QC equipment.
• Contribute to the continuous improvement of laboratory processes and test methods.
• Assist in creating and updating process and product documentation.
• Support Research & Development (R&D) activities by assisting with testing for new technologies and product/process improvements.
• Act as a key liaison between the QC lab, manufacturing, R&D, and engineering teams to ensure seamless communication and collaboration.
• Perform other duties as assigned.