Analytical Chemist II – HPLC/GC (Temporary Contract) - Eurofins Cosmetics & Personal Care, Inc.

Eurofins•Toronto, ON

20d•CA$24 - CA$26•Hybrid

About The Position

Reporting directly to the Department Head - Chemistry, the Analyst II will be responsible for providing basic technical support and analysis within the Cosmetic and Personal Care Product Testing Laboratory. This is a high-pressure work environment with meeting tight deadlines, multitasking on several projects for a variety of clients. The Analyst II will have over 5 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. A suitable candidate must be energetic, well-organized, self-disciplined and flexible. Excellent and efficient communication is a mandatory requirement in order to interact within the Team and with other staff members, 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

Over 5 years of laboratory testing experience
Demonstrated ability to complete more complex role/duties
Handled variety of instrumentation for analytical testing
Able to work independently with minimal/no supervision
Energetic, well-organized, self-disciplined and flexible
Excellent and efficient communication is a mandatory requirement
High level of professionalism and confidentiality is crucial
Proficient in operating HPLC and GC
Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs)
Analyze APIs and Finished products for Assay, Impurities, Identification and Limit test studies 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, methods, protocols as required
Assisting in instrument calibration/qualification/maintenance in co-operation with Calibration Team
Proficient in Microsoft office programs (Outlook, Word, and Excel)
Hands on experience with analytical data acquisition software e.g. Chromeleon, e-LIMS, ETQ etc
Troubleshoot technical issues/ difficulties with methods and instruments
Perform Method Transfers and Method Validations in coordination with Dept.Head
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 wet chemistry methods and procedures, such as Specific Gravity, Viscosity, Water Determination by KF, etc.
Strong interpretation of routine analysis or tests
Have In-depth understanding of chromatography principles, types and techniques
Have high troubleshooting skills, both with instruments and methods
Be able to write clear, attributable lab reports with minimal to no corrections
Be able to read, understand and interpret any type of Pharmacopoeia, including the references to general chapters
Be able to work under GMP guidelines, and be proficient with USP/EP/BP testing
Write Method Modifications and Method Review Forms in accordance with internal procedures
Be competent in research and study skills to learn about innovative methodologies and equipment used for problem solving and troubleshooting
Be accountable for the integrity and traceability of all data generated and reported
Order necessary supplies and study materials and assist in writing procedure manuals
Perform other duties as assigned by 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 trouble shoot instrumentation/methods
Perform other departmental tasks such as cleaning, supply ordering, logbooks review
Perform analytical tests utilizing HPLC/UPLC, GC, UV, IR, FTIR, KF and other laboratory instruments
Mentoring/training junior staff members
Calibration and preventive maintenance of HPLC/GC etc
Writing SOPs
Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method
Participation in meetings and routine Lab Support Operations, contribution to Lab Audit preparations in assistance with tasks assigned by QA and QC Management
A B.Sc. degree in Chemistry, Biochemistry, or diploma in related filed
A solid background and understanding of Chemistry is mandatory
Computer proficiency- Microsoft Office, especially Excel
5-10 years working with analytical instrumentation
Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods

Nice To Haves

Experience working in contract Laboratory considered an asset
Experience working with GC-MS is an asset
Experience working with Cosmetic Products, such as creams, lotions, ointments and other challenging matrixes

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, logbooks review
Perform analytical tests utilizing HPLC/UPLC, GC, UV, IR, FTIR, KF and other laboratory instruments
Mentoring/training junior staff members
Calibration and preventive maintenance of HPLC/GC etc
Writing SOPs
Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method
Participation in meetings and routine Lab Support Operations, contribution to Lab Audit preparations in assistance with tasks assigned by QA and QC Management
Proficient in operating HPLC and GC
Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs)
Analyze APIs and Finished products for Assay, Impurities, Identification and Limit test studies 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, methods, protocols as required
Assisting in instrument calibration/qualification/maintenance in co-operation with Calibration Team
Proficient in Microsoft office programs (Outlook, Word, and Excel)
Hands on experience with analytical data acquisition software e.g. Chromeleon, e-LIMS, ETQ etc
Troubleshoot technical issues/ difficulties with methods and instruments
Perform Method Transfers and Method Validations in coordination with Dept.Head
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 wet chemistry methods and procedures, such as Specific Gravity, Viscosity, Water Determination by KF, etc.
Strong interpretation of routine analysis or tests
Have In-depth understanding of chromatography principles, types and techniques
Have high troubleshooting skills, both with instruments and methods
Be able to write clear, attributable lab reports with minimal to no corrections
Be able to read, understand and interpret any type of Pharmacopoeia, including the references to general chapters
Be able to work under GMP guidelines, and be proficient with USP/EP/BP testing
Write Method Modifications and Method Review Forms in accordance with internal procedures
Be competent in research and study skills to learn about innovative methodologies and equipment used for problem solving and troubleshooting
Be accountable for the integrity and traceability of all data generated and reported
Order necessary supplies and study materials and assist in writing procedure manuals
Perform other duties as assigned by Laboratory Manager