Role and Location
Scientist III - LCMS - Pharma
Location: GMP Laboratory in Athlone. This position provides testing services to our clients as part of Thermo Fisher Scientific’s PPD Laboratory Services team, focused on delivering accurate laboratory analysis of pharmaceutical products using analytical instrumentation and data analysis. The role includes acting as project leader on multiple projects, interacting with clients, reviewing data, writing reports and protocols, and communicating regulatory issues with senior team members.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) and safety standards.
Discover Impactful Work
Our work spans laboratory, digital and decentralized clinical trial services. This role supports clinical trials conducted in 100+ countries and contributes to the ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio. Your work aims to improve health outcomes for patients and communities now and in the future.
What You’ll Do
* Independently performs method validations, method transfers, and analytical testing of pharmaceutical compounds in a variety of formulations.
* Designs and completes experiments with minimal supervision.
* Prepares study protocols, project status reports, final study reports and other project-related technical documents.
* Communicates data and technical issues to the client and responds to client needs.
* Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instruments and analytical problems.
* Assists in designing method validation or method transfer protocols and establishing project timelines.
* Reviews data for technical, quality and compliance to protocols, methods, SOPs, client criteria and GMP.
Education & Experience
* Bachelor’s degree in a relevant area (e.g., chemistry, biochemistry).
* 5+ years of relevant industry experience within a GMP laboratory with experience handling LCMS instrumentation (e.g., LCMS-QQQ/Sciex 6500 or similar, Orbitrap or other high-resolution LCMS) and with complex data evaluation and processing.
* Experience in Method Validation, Method Transfer and Analytical testing.
* Equivalency considerations may apply (education, training and/or directly related experience).
Knowledge, Skills, Abilities
* Detailed knowledge of method validation; method development is a plus.
* Ability to plan, schedule and carry out work for successful project completion.
* Positive attitude and ability to work well with others.
* Excellent attention to detail.
Our mission is to enable our customers to make the world healthier, cleaner and safer. We value integrity, intensity, innovation and involvement as a united team of 100,000+ colleagues.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility services for job seekers requiring accommodations in the job application process. If you require accessibility assistance or accommodations to apply, please submit a request by telephone at 1-855-471-2255. The line is reserved for job seekers requiring accessibility assistance; messages for other purposes may not receive a response.
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