Analyst I - Eurofins BioPharma Product Testing Toronto, Inc. at Eurofins

Toronto, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

16 Jan, 26

Salary

0.0

Posted On

18 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Testing, ICP-OES, ICP-MS, Atomic Absorption Spectrometer, Method Development, Method Validation, Sample Preparation, Data Analysis, Troubleshooting, Good Manufacturing Practices, Documentation, Chromatography, Research Skills, Technical Judgment, Safety Compliance, Microsoft Office

Industry

Medical and Diagnostic Laboratories

Description

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, 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 Director - Chemistry, the Analyst I 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 I will have over 2 to 5 years of laboratory testing experience with demonstrated ability to complete role/duties that are more complex. 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. The Analyst I must: Perform method development, method validation, method transfer and routine analyses using ICP-OES , ICP-MS and Atomic absorption spectrometer instrumentation. Review data, prepare protocols and reports to ensure Chemistry projects meet the timeline. Train new Analysts to perform ICP-MS techniques. Perform sample preparation and analysis and execute a number of routine/non-routine methods and procedures including method development, validation, verification and sample testing. Perform instrument calibration, qualification and preventative maintenance program as necessary. Perform investigations and troubleshoot non-confirmatory results or methods. 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 of multiple elements, heavy metals. Recognizes OOS or out of trend results and assist laboratory manager in the completion of lab investigations. Process and report analytical results. Update and report work into LIMS. 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. Syngistix, e-LIMS, ETQ etc. Troubleshoot technical issues/ difficulties with methods. Co-ordinate 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 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. Apply technical judgment to determine potential problems for samples. 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 using various wet chemistry techniques, extraction of heavy metals using conventional digestion/microwave digestion techniques 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 ICP-OES, ICP-MS and Atomic absorption spectrometer, 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 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: 2-5 years working with analytical instrumentation in particular ICP-MS, ICP-OES and Atomic absorption spectrometer. Ability to work directly from the USP or EP pharmacopeia and execute methods Experience working in contract Laboratory considered an asset. Experience working with Pharmaceuticals. Additional Information At Eurofins we offer excellent full-time 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 e-mail a request via the website at www.eurofins.ca. 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 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. This posting is supported by AI technology to assist in screening candidates and resumes. NO AGENCIES, CALLS OR EMAILS PLEASE

Responsibilities

The Analyst I will provide technical support and analysis in the Biopharmaceutical Chemistry Testing Laboratory, ensuring projects meet deadlines. Responsibilities include method development, data review, training new analysts, and maintaining compliance with safety policies.