Analyst II (HPLC) - Eurofins BioPharma Product Testing Toronto, Inc.

Eurofins Humangenetik & Pränatal-Medizin; Old Toronto; On-site; CAD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a dynamic Analyst II to join their Biopharmaceutical Chemistry Testing Laboratory. In this full-time role, you will provide essential technical support and analysis, working with sophisticated equipment to ensure compliance with industry standards. With a focus on HPLC and GC methodologies, you will thrive in a fast-paced environment, contributing to various projects while maintaining a high level of professionalism. This is a fantastic opportunity to advance your career in a supportive and innovative setting that values your expertise and dedication.

Benefits

Health and dental coverage

Life and disability insurance

RRSP with 3% company match

Paid holidays

Paid time off

Qualifications

• 5-10 years of laboratory testing experience with analytical instrumentation.
• Proficient in HPLC, GC, and LC-MS/MS with strong documentation skills.

Responsibilities

• Conduct analysis using HPLC and other laboratory instruments.
• Prepare samples and ensure compliance with GMP and SOPs.
• Mentor junior staff and maintain accurate documentation.

Skills

HPLC

GC

LC-MS/MS

Chromatography principles

Analytical instrumentation

Troubleshooting

Documentation skills

Education

B.Sc. degree in Chemistry

Diploma in related field

Tools

Empower

Chromeleon

e-LIMS

Microsoft Office (Excel, Word, Outlook)

Job description

Analyst II (HPLC) - Eurofins BioPharma Product Testing Toronto, Inc.

• Full-time

Basic Function: 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 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. 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.

The Analyst II must:

• 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.

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 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 (SOPs) and the current test method.
• Participates in general lab duties, including clean-up, administration, logbook review and operations support.

Education:

• A B.Sc. degree preferably in Chemistry, or diploma in related field.
• 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.

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

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

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.