Quality Control Analyst - cGMP Lab for Therapeutics

PEI BioAlliance; Charlottetown; On-site; CAD 50,000 - 78,000; Full time

Benefits offered by this job

Bonus

Stock options

Benefits

Job summary

BIOVECTRA, a leading contract development and manufacturing organization within Agilent, is seeking a Quality Control Analyst in Charlottetown, Canada. The role focuses on analytical testing and bench chemistry in a fast-paced lab, with responsibilities spanning data reporting and release documentation.

The ideal candidate holds a science-related degree with experience in HPLC, GC, KF, and cGMP environments, demonstrating strong attention to detail and safe handling of chemicals.

Qualifications

• Post-secondary education in a scientific field.
• Bachelor’s degree in Chemistry, Biology, Biochemistry, or related science.
• Experience with HPLC, GC, and Karl Fischer (KF) analysis.
• Experience in a cGMP-regulated environment.
• Strong analytical skills and attention to detail in a fast-paced lab setting.

Responsibilities

• Perform analytical testing using HPLC, GC, UV-Vis, and NMR.
• Conduct bench chemistry testing, including TLC, titrimetry, and gravimetry.
• Maintain accurate laboratory records and documentation.
• Perform calculations and support data reporting.
• Conduct routine instrument maintenance and calibration.
• Prepare material release documentation and Certificates of Analysis.
• Track and manage laboratory samples.
• Identify and report out-of-specification (OOS) results.
• Safely handle chemicals, solvents, APIs, and other hazardous materials.

Skills

Attention to detail

Analytical skills

Laboratory teamwork

Education

Post-secondary science education

Bachelor’s degree in Chemistry/Biology/Biochemistry

Tools

HPLC

GC

Karl Fischer

NMR

UV-Vis

Job description

BIOVECTRA, a leading contract development and manufacturing organization within Agilent, is seeking a Quality Control Analyst in Charlottetown, Canada. The role focuses on analytical testing and bench chemistry in a fast-paced lab, with responsibilities spanning data reporting and release documentation.

The ideal candidate holds a science-related degree with experience in HPLC, GC, KF, and cGMP environments, demonstrating strong attention to detail and safe handling of chemicals.