HPLC Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

Eurofins•Toronto, ON

65d•CA$50,000 - CA$50,000•Onsite

About The Position

Reporting directly to the Department Head - Chemistry, the Analyst 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 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.

Requirements

5-10 years working with analytical instrumentation.
Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods.
A solid background and understanding of Chemistry is mandatory.
Computer proficiency- Microsoft Office , especially Excel.

Nice To Haves

Experience working in contract Laboratory considered an asset.
Experience working with Pharmaceuticals.

Responsibilities

Proficient in operating GC/HPLC/LC-MS/MS/GC-MS.
Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
Analyze API, Raw Materials and Finished products for Assay, Impurities & Dissolution study using HPLC /GC instrument with minimum supervision.
Recognizes OOS or out-of-trend results and assists laboratory manager in the completion of lab investigations.
Review technical data, documents, and proposals as required.
Proficient in Microsoft office programs (Outlook, Word, and Excel).
Hands-on experience with pharmaceutical data acquisition software e.g. Empower and Chromeleon, e-LIMS, ETQ etc.
Troubleshoot technical issues/ difficulties with methods.
Coordinate with team members to perform method transfers between R&D group to QC group.
Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.
Be experienced in a wide variety of routine and some non-routine wet chemistry methods and procedures.
Strong interpretation of routine analysis or tests.
In-depth understanding of chromatography principles, types and techniques.
Have high troubleshooting skills, both with instruments and methods.
Be able to write lab reports.
Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods.
Be able to work under GMP guidelines, and be proficient with USP and pharmaceutical testing.
Explaining latest, applicable methods and techniques to perform various experiments and teaching necessary techniques that need to be adopted to complete a particular experiment or an allotted assignment.
Competent research and study skills to learn about innovative methodologies and equipment used for problem-solving and troubleshooting.
Accountable for the integrity and traceability of all data generated and reported.
Design, preparation, and production of study materials including procedure manuals.
Perform other duties as assigned by the Laboratory manager.
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 troubleshoot 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 (SOP) and the current test method.
Participates in general lab duties, including clean-up, administration, logbook review and operations support.