About The Position

Working closely with the Team Lead, this position will lead complex analytical testing, method troubleshooting, and sample disposition decisions. As part of this role, you will provide technical leadership, mentorship, training, and support for continuous quality and regulatory compliance. This role is on our split day shift of which you will be the senior responsible on closing the lab.

Requirements

  • DEC in Science or Chemistry/ bachelor’s degree in chemistry
  • 5+ years in QC Analytical laboratory (pharmaceutical), with demonstrated leadership
  • Strong expertise in HPLC/ GC/ MS, statistical analysis
  • Experience working in a cGMP environment with an understanding of FDA, ICH and USP regulations
  • Ability to work independently on routine tasks with some supervision for more complex tasks
  • Capable of managing multiple tasks and projects with guidance ensuring deadlines are met
  • Attention to detail with a focus on maintaining quality and consistency in results
  • Strong analytical reasoning and problem-solving skills
  • Effective written and oral communication; ability to write and present findings
  • High integrity and commitment to data quality, GMP compliance
  • Adaptable and willing to take on any task in the lab when needed (including cleaning) to support team success

Responsibilities

  • Perform and review complex analytical testing (advanced HPLC/UPLC, GC, mass spectrometry, dissolution profiling, assays, UV-VIS) and interpret results.
  • Lead investigations of OOS/OOT results, nonconformances, deviations, and CAPAs; author technical sections of investigation reports.
  • Provide technical guidance and mentoring to Level 1–2 staff, lead side-by-side and data review for training and mentoring competency assessments.
  • Review and approve QC documentation, batch release testing records, and analytical data for accuracy and compliance.
  • Maintain and perform advanced instrument troubleshooting, preventative maintenance planning, and liaise with service vendors.
  • Contribute to continuous improvement initiatives (process optimization, data integrity, automation).
  • Assist in method transfers as required, support validation and cleaning method qualification activities.
  • Support audits and regulatory inspections; prepare technical responses and action plans.
  • Ensure adherence to GM, data integrity principles, and laboratory safety.

Benefits

  • Competitive Salary
  • Comprehensive Health Benefits
  • Group RRSP (with 4% match program)
  • Annual Vacation and additional Personal Time Off (PTO) program
  • Health and Wellness Support Programs (Homewood Health EAP & Telus Health Virtual Care)
  • Team building and fun corporate events
  • And you’ll join a diverse and multi-disciplinary team!
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service