Analyst II - Eurofins BioPharma Product Testing Toronto, Inc.

at  Eurofins Canada BioPharma

IN 2023, EUROFINS GENERATED TOTAL REVENUES OF EUR 6.515 BILLION, AND HAS BEEN AMONG THE BEST PERFORMING STOCKS IN EUROPE OVER THE PAST 20 YEARS.

Job Description
Reporting directly to the Department Head - Chemistry, the Analyst II will be responsible for providing basic technical support and analysis within the Biopharmaceutical Chemistry Testing Laboratory. This is a deadline-based, high-pressure work environment with on-going projects for a variety of clients.
The Analyst II will have over 5 to 10 years of laboratory testing experience with demonstrated ability to complete more complex role/duties. Has handled variety of instrumentation for analytical testing and will be able to work independently with minimal/no supervision. The incumbent must be energetic, exceedingly well-organized, flexible, and must have the ability to interact with customers and staff in a fast-paced environment, sometimes under pressure, while remaining proactive, resourceful, and efficient. A high level of professionalism and confidentiality is crucial to this role.

EDUCATION:

• A B.Sc. degree preferably in Chemistry, or diploma in related filed.
• A solid background and understanding of Chemistry is mandatory
• Computer proficiency- Microsoft Office , especially Excel

EXPERIENCE:

• 5-10 years working with analytical instrumentation.
• Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods
• Experience working in contract Laboratory considered an asset.
• Experience working with Pharmaceuticals.

• Sample preparation and Mobile phases preparation;
• Documentation: Ensuring accurate reporting in lab books.
• Using a wide range of sophisticated equipment and instruments to conduct analysis and research and trouble shoot instrumentation/methods
• Perform other departmental tasks such as cleaning, supply ordering, assist with instrumentation training and maintenance, etc
• Perform analytical tests utilizing HPLC/UPLC, GC, UV, IR, FTIR, KF and other laboratory instruments.
• Assess, compare and perform risk assessments for compendial method compliance according to USP, EP, and other regulations
• Mentoring/training junior staff members and Imparting training to new recruits for operation, calibration and preventive maintenance of GCMS/GC/HPLC/ LC-MS/MS, etc .
• Writing SOPs
• Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method.
• Participates in general lab duties, including clean up, administration, logbook review and operations support
  Qualifications