LCMS/MS & GCMS/MS Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

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

Job summary

Join a leading international life sciences company as an LCMS/MS & GCMS/MS Analyst, where your expertise in method development and validation will play a crucial role in ensuring the safety and quality of products. In this full-time position, you will work in a dynamic laboratory environment, conducting analyses and troubleshooting technical issues while mentoring junior staff. The company offers a collaborative atmosphere and excellent benefits, making it an ideal place for professionals looking to make a significant impact in the pharmaceutical and biopharmaceutical fields. If you thrive in a fast-paced setting and are committed to quality, this opportunity is perfect for you.

Benefits

Health & Dental Coverage

Life Insurance

Disability Insurance

RRSP with 3% Company Match

Paid Holidays

Paid Time Off

Qualifications

• 3-5 years in Pharmaceutical/Biopharmaceutical field in a GMP environment.
• Strong experience in Method Development and Validation.
• Solid background in Mass Spectrometry is mandatory.

Responsibilities

• Perform Method Development, Validation, and Routine Analysis using LCMSMS and GCMSMS.
• Troubleshoot technical issues and manage multiple research projects.
• Guide and mentor junior staff members to achieve quality metrics.

Skills

Method Development

Method Validation

Analytical Laboratory Skills

Organizational Skills

Communication Skills

Attention to Detail

Multitasking

Education

Bachelor of Science in Chemistry

Diploma in a Related Field

Tools

MS Office

LIMS

Empower

MassHunter

Analyst Software

HPLC

GC

Job description

LCMS/MS & GCMS/MS Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

• Full-time

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.

Under the direction of Department Head of R&D, the LCMS/MS & GCMS/MS analyst would be responsible for supporting the department in analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory that meets departmental goals.

Key Responsibilities:

• Perform Method Development, Method Validation, Method Transfer and Routine Analysis using LCMSMS and/or GCMSMS instrumentation techniques.
• Review data, prepare protocol and report to ensure R&D projects meet the timeline.
• Troubleshoot technical issues/difficulties with all tests related to Analytical Laboratory.
• Perform instrument calibration, qualification and preventative maintenance as necessary.
• Manage multiple research projects simultaneously to meet project timelines.
• Verify that all study materials (including standards, reagents and columns) are in stock.
• Perform investigations and troubleshoot non-confirmatory results or methods.
• Understand and follow Quality System documents relevant to responsibilities, e.g. Quality Manual, SOPs, GMP/GLP/USP and Methods.
• Adhere to appropriate quality measures to meet or exceed standards set by GMP government regulatory and company requirements relevant to assigned duties.
• Maintain a neat and accurate record system of daily activities related to all R&D and Quality Control testing.
• Guide, mentor and train junior staff members to achieve expected quality and TAT metrics.
• Any tasks as required by supervisor or Management in all aspects of business to meet departmental goals.

EXPERIENCE:

• A minimum of 3-5 years working experience in the Pharmaceutical/Biopharmaceutical field, in a GMP environment.
• Strong experience with Method Development, Method Validation, Method Transfers study.
• Computer proficiency in MS Office (Outlook, Word, Excel), LIMS, Empower, MassHunter & Analyst Software in a GMP environment.
• HPLC & GC experience would be an asset.

Education:

• Bachelor of Science in Chemistry or diploma in a related field.
• A solid background in Mass Spectrometry is mandatory.

Other Required Skills:

• Excellent organizational skills.
• Strong verbal and written communication skills.
• A good command of English is necessary.
• High level of accuracy and strong attention to detail.
• Ability to work independently while supporting a collaborative, team-based department.
• Ability to multitask and remain calm under pressure.
• Must be able to work in a fast-paced environment and meet deadlines.
• Must be proactive, self-disciplined, and able to demonstrate a high level of productivity.
• Demonstrate satisfactory work performance and attendance record.
• Display a high level of professionalism.
• Willingness to learn with the ability to retain information quickly and apply knowledge to various scenarios.

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.

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.

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.