Job opportunity
Pharmaceutical Quality Control Analyst
Agilent Technologies, Inc.
Support pharmaceutical material release as a Quality Control Chemist with BIOVECTRA in Windsor, Nova Scotia, using precise 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.
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Apply on source site 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.
#J-18808-Ljbffr