Scientist III, Biopharma - Core & Morning shift - Athlone, Ireland at Thermo Fisher Scientific
Athlone, County Westmeath, Ireland -
Full Time


Start Date

Immediate

Expiry Date

15 Nov, 25

Salary

0.0

Posted On

16 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Training, Wellbeing, Method Transfer, Diverse Groups, Electrophoresis, Life Sciences, Office Equipment, Method Development, Technology

Industry

Pharmaceuticals

Description

JOB DESCRIPTION

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

EDUCATION

  • Bachelor’s degree (life sciences preferred) or equivalent and relevant formal academic / vocational qualification

EXPERIENCE

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ 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

  • 5+ years’ relevant industry experience within a GMP laboratory (with experience in the following lab testing areas HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry.
  • Experience in Method Validation, Method Transfer and Analytical testing.
  • Detailed knowledge of method validation; method development would be an advantage.
  • The ability to plan, schedule and carry out work for successful project completion
  • A positive attitude and ability to work well with others
  • Excellent attention to detail

How To Apply:

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Responsibilities
  • 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 successfully under pressure while prioritizing and handling multiple projects or activities
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