- Conduct Method Development, Validation, Transfer, and Routine Analysis utilizing LCMSMS and/or GCMSMS techniques.
- Review data, prepare protocols, and reports to ensure R&D projects adhere to timelines;
- Troubleshoot technical issues/ difficulties in all tests related to the Analytical Laboratory;
- Perform instrument calibration, qualification, and preventative maintenance as needed;
- Manage multiple research projects simultaneously to meet deadlines;
- Ensure availability of all study materials in stock;
- Conduct investigations and troubleshoot non-confirmatory results or methods;
- Comprehend and adhere to relevant Quality System documents such as Quality Manual, SOPs, GMP/GLP/USP, and Methods;
- Follow appropriate quality measures to meet GMP regulatory standards;
- Maintain an accurate record system of daily activities related to R&D and Quality Control testing;
- Guide, mentor, and train junior staff members for quality and TAT metrics;
- Perform any tasks as assigned by supervisors or Management to achieve departmental goals.
- Minimum 3-5 years of experience in Pharmaceutical/Biopharmaceutical field, in a GMP setting;
- Proficiency in Method Development, Validation, and Transfer;
- Computer skills in MS Office, LIMS, Empower, MassHunter & Analyst Software;
- Preferable experience in HPLC & GC.
- Bachelor of Science in Chemistry or related diploma;
- Strong background in Mass Spectrometry.
- Strong organizational skills;
- Effective verbal and written communication;
- Proficient in English with high accuracy and attention to detail;
- Ability to work independently and in a team-based environment;
- Effective multitasking and remaining composed under pressure;
- Proactive, disciplined, and productive attitude;
- High professionalism and willingness to learn quickly;
- Ability to retain information and apply knowledge effectively.
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Eurofins Toronto, Canada Full timeJob Description · Under the direction of Department Head of R&D, LCMS/MS& GCMS/MS analyst would be responsible for supporting the department for analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory that meets the departmental goal. · Key Responsibilities: · Per ...
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Eurofins Toronto, Canada Full timeCompany 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 th ...
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LCMS/MS & GCMS/MS Analyst - Eurofins BioPharma Product Testing Toronto, Inc - Eurofins Canada BioPharma
Description
Job DescriptionUnder the supervision of the R&D Department Head, the LCMS/MS & GCMS/MS analyst will be responsible for supporting the department in analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory to achieve departmental objectives.
Key Responsibilities:
EXPERIENCE:
Education:
Other Required Skills:
Working Conditions: This role will be in a laboratory environment, requiring standing for over 50% of the time and light lifting of up to 20 lbs.
Additional InformationAt Eurofins, we provide comprehensive benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, and paid time off.
Accommodations: Requests for accommodation in the application process or alternative job posting formats may be made via the website.
As a Eurofins team member, you join a company known internationally as a great workplace. Explore our website to learn more about Eurofins.
We appreciate applicants within commuting distance of GTA, Ontario for their interest. Only selected candidates will be contacted for an interview.
NO AGENCIES, CALLS, OR EMAILS PLEASE.
LCMS/MS & GCMS/MS Analyst - Eurofins BioPharma Product Testing Toronto, Inc professionals in Toronto
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jason ji
.NET Framework. C#, Web Services, T-SQL, BizTalk