Apply HPLC and GC expertise as a Quality Control Analyst with BIOVECTRA, part of Agilent, on a full-time swing shift. Support pharmaceutical testing through precise laboratory analysis.
This Quality Control Analyst performs analytical and bench chemistry testing in a laboratory environment. The work supports production of life-changing pharmaceutical therapies through documentation, calculations, sample management, and data reporting. Preferred experience includes HPLC, GC, Karl Fischer analysis, and cGMP operations.
Key Responsibilities:
- Perform HPLC, GC, UV-Vis, and NMR analytical testing
- Conduct TLC, titrimetry, and gravimetry bench chemistry testing
- Maintain accurate laboratory records and documentation
- Prepare material release documents and Certificates of Analysis
- Identify and report out-of-specification results
Requirements:
- Post-secondary education in a scientific field
- Bachelor's degree in Chemistry, Biology, Biochemistry, or related science preferred
- Experience with HPLC, GC, and Karl Fischer analysis preferred
- Experience in a cGMP-regulated environment preferred
- Strong analytical skills and attention to detail
Use analytical testing, laboratory documentation, and pharmaceutical quality skills to support BIOVECTRA's manufacturing operations.
Quality Control Analyst HPLC GC employer: Allozymes
BIOVECTRA, now part of Agilent, is an exceptional employer located in Windsor, NS and Charlottetown, PEI, offering a dynamic work culture that prioritizes innovation and collaboration. Employees benefit from competitive compensation, comprehensive health benefits, and opportunities for professional growth within the cutting-edge field of advanced manufacturing. Joining our team means contributing to meaningful advancements in patient care while working alongside dedicated professionals in a supportive environment.
