Assoc Research Scientist (Technical Lead), Cell & Molecular Biology - Athlone, Ireland

Thermo Fisher Scientific View all jobs

  • Athlone, Co Westmeath
  • Permanent
  • Full-time
  • 2 months ago
Work Schedule Standard (Mon-Fri)Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob DescriptionJob DescriptionPosition: Associate Research ScientistAt 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 through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized 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 InformationJoin our Cell Lab team in Ireland, where you will be part of our dynamic research team dedicated to advancing science and technology.Discover Impactful Work:As an Associate Research Scientist you will be responsible for the regulatory and scientific conduct of development, validation, stability projects, and/or other specialty technologies. In this role you will perform troubleshooting on multiple analytical techniques, calculate and interpret data, and record data in adherence with PPD SOPs and any additional requirements specific to the lab and/or client. The Associate Research Scientist routinely acts as the technical project leader for multiple projects, interacts with clients on a weekly basis, or as needed, to provide updates, review and evaluate data, and write reports and protocols.A Day in the Life:
  • Independently performs analytical testing, method optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods, and protocols applicable to assigned tasks. Designs and executes experiments independently.
  • Reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.
  • Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents.
  • Communicates data and technical issues to clients on a weekly basis (or as needed).
  • Provides technical guidance and training to staff.
  • Leads analytical (procedural and instrumental) troubleshooting sessions.
  • Assists in preparation and implementation of SOPs and quality systems.
  • 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.
Keys to Success:Education and Experience:
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 6+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills, Abilities
  • Demonstrated experience with method development and validation, Cell based assays and experience in molecular biology preferable.
  • Ability to independently perform root cause analysis for method investigations
  • Proficiency on technical operating systems
  • Proven problem solving and troubleshooting abilities
  • Proven ability in technical writing skills
  • Time management and project management skills
  • Good written and oral communication skills
  • Ability to work in a collaborative work environment with a team
  • Ability to train junior staff
BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!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.comThermo 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.We welcome and encourage applicants from outside of Ireland. We can provide support with immigration and visa needs for successful applicants and dependents. All other relocation costs are at the expense of the applicant.

Thermo Fisher Scientific