Laboratory Analyst – Established Pharmaceuticals

4 weeks ago

Victoriaville, Quebec, Canada Abbott Full time

Position Overview

This role is situated within the Established Pharmaceuticals division, where our focus is on delivering the advantages of our reliable medications to a broader audience in rapidly developing regions. Our extensive range of high-quality branded generic medicines spans various therapeutic areas, including gastroenterology, women's health, cardiometabolic conditions, pain management, and respiratory health.

Key Responsibilities

Quality Control Analysis:
• Conduct sampling and analysis of raw materials, in-process products, and finished goods in accordance with the quality control standards;
• Analyze final products, including preparation of standards for HPLC and mobile phases, while interpreting results;
• Prepare various solutions necessary for analysis;
• Calibrate laboratory instruments as per standard operating procedures (SOPs);
• Relay pertinent information to relevant personnel;
• Maintain comprehensive records of all tests, procedures, and results, including stability studies, and report non-compliance findings to the QC Supervisor or QA/QC Manager;
• Prepare labels for the release of raw materials and finished products;
• Execute analyses in compliance with safety regulations and good manufacturing practices (GMP);
• Ensure a clean laboratory environment and adhere to health and safety protocols;
• Contribute to the development of SOPs.

Subject Matter Expert Support:
• Revise laboratory procedures for new systems, updates, or corrective measures;
• Oversee calibration and maintenance schedules for laboratory equipment;
• Implement and evaluate new laboratory instruments and systems;
• Monitor and follow up on validations conducted by the QC laboratory;
• Update and analyze laboratory key performance indicators (KPIs) and trends for monitored products and systems;
• Assist in troubleshooting analytical techniques or instrument-related issues;
• Serve as a backup for audit representation concerning laboratory activities.

Technical Advisory Support:
• Conduct laboratory investigations for events impacting the QC laboratory;
• Manage communication and reception of external laboratory analyses;
• Provide analytical support to scientific and technical teams;
• Facilitate training on equipment, techniques, and procedures relevant to the QC laboratory.

Continuous Improvement and Innovation:
• Actively participate in meetings with production and QA-QC departments;
• Strive for ongoing enhancement of methods, procedures, equipment, and techniques within the QC department, proposing improvements where applicable;
• Contribute to the advancement of new techniques and methods for routine, non-routine, and project-related tasks.

Additional Responsibilities:
• Engage in the implementation of lean continuous improvement methodologies within the QC laboratory;
• Foster a collaborative work environment that promotes team effectiveness.

Qualifications:
• A college degree in a scientific discipline (Chemistry, Biochemistry, etc.) and a minimum of 3 years of experience in the pharmaceutical or related sectors. Strong knowledge of chemistry, particularly HPLC;
• Over 5 years of experience in a comparable position;
• Proficient in both written English and French;
• Competent in computer applications (Microsoft Suite);
• Capable of thriving in a continuous improvement setting (LEAN principles).

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