Support pharmaceutical material release as a Quality Control Chemist with BIOVECTRA in Windsor, Nova Scotia, using exact analytical testing and documentation practices.
BIOVECTRA, now part of Agilent, is hiring a full-time permanent chemist for its quality control function. The position involves testing pharmaceutical materials, tracking samples, documenting laboratory activities, and recognizing results outside specifications. You will also support analytical method validation and prepare technical procedures for laboratory work.
Key Responsibilities:
- Complete analyses using instrumental and electrophoretic techniques
- Track and log samples throughout laboratory workflows
- Prepare release documentation, status labels, and certificates
- Support analytical method validation and verification activities
- Write SOPs for testing and sample handling procedures
Requirements:
- Recognized Chemical Technology diploma
- Chemistry, Biochemistry, or related science degree preferred
- Experience with GC, HPLC, UV-VIS, PCR, or plate readers preferred
- Knowledge of cGMP guidelines considered an asset
- Willingness to work rotating 12-hour shifts
Use quality control chemistry, sample management, and technical writing skills supporting BIOVECTRA’s pharmaceutical operations.