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Athlone
Athlone, Ireland
Regular Full Time
Regular Full Time
Analytical chemist, Gas chromatography, Molecular spectroscopy UV-Vis, RAMAN, FTIR
Analytical chemist, Gas chromatography, Molecular spectroscopy UV-Vis, RAMAN, FTIR

Scientist I (Assoc Scientist)

Inactive
Thermo Fisher Scientific - Career

As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.

Scientist I (Assoc Scientist)

At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralised clinical trial services.

Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations

Discover Impactful Work:

As a Scientist I (Assoc Scientist) Pharma you will perform a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical compounds in a variety of formulations.

A Day in the life:

  • Follows validated or experimental analytical procedures with periodic direct supervision.
  • Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.
  • Problem solves with assistance pertaining to extraction and/or instrumentation problems.
  • Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
  • Handles QC/QA responsibilities without supervisor or QA input.
  • Communicates project status to project leader.
  • Performs work assignments accurately, and in a timely and safe manner.
  • Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
  • Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers. 

Education & Experience

  • B.S./B.A. in Chemistry or related field with of 1 years’ experience in analytical testing laboratory.
  • 1+ years in an analytical environment with experience utilising HPLC  
  • Other techniques should include GC, KF, UV-Vis, FT-IR, etc.
  • Ideally experience with device testing, using materials testing systems, for pre-filled syringes and auto-injectors would be a bonus

Knowledge, Skills, Abilities

  • Knowledge of applicable regulatory authority, compendium and ICH guidelines
  • Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use
  • Ability to utilise Microsoft Excel and Word to perform tasks
  • Ability to independently optimise analytical methods
  • Good written and oral communication skills
  • Time management and project management skills
  • Proven problem solving and troubleshooting abilities
  • Ability to work in a collaborative work environment with a team

Work Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to build a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary and/or standing for typical working hours.
  • Able to lift and move objects up to 25 pounds.
  • Able to work in non-traditional work environments.
  • Able to use and learn standard office equipment and technology with proficiency.
  • May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
  • Able to perform optimally under pressure while prioritizing and balancing multiple projects or activities.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

We welcome and encourage applicants from outside of Ireland.  We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services.  All other relocation costs are at the expense of the applicant.

Work Schedule

  • Standard (Mon-Fri)

Environmental Conditions

  • Adherence to all Good Manufacturing Practices (GMP) Safety Standards
 

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