Analyst II - Eurofins BioPharma Product Testing Toronto Inc

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 deadlinebased highpressure work environment with ongoing 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 wellorganized flexible and must have the ability to interact with customers and staff in a fastpaced environment sometimes under pressure while remaining proactive resourceful and efficient. A high level of professionalism and confidentiality is crucial to this role.

The Analyst II must:

• Proficient in operating GC/HPLC/LCMS/MS/GCMS
• 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 assist 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 eLIMS 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 on a number of wide variety  of routine and some nonroutine wet chemistry methods and procedures;
• Strong interpretation of routine analysis or tests.
• Indepth 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 Laboratory manager.

Key Responsibilities:

• 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/ LCMS/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 :

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:

• 510 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.

WORKING CONDITIONS

• This position will be working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses. Light lifting requirements of no more than 20 lbs.
• Shift work and overtime may be required as well as working periodic weekends and/or evenings.

Additional Information :

At Eurofins we offer excellent fulltime benefits including health & dental coverage life and disability insurance RRSP with 3% company match paid holidays paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process or those needing job postings in an alternative format may email a request via the website at 

As a Eurofins employee you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins please explore our website at 

We thank all applicants within commuting distance of GTA Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

NO AGENCIES CALLS OR EMAILS PLEASE

Remote Work :

No

Employment Type :

Fulltime