Study Lead - Pharma

Thermo Fisher Scientific
Athlone, Leinster, Ireland
Full Time
On Site
Senior
0+
Bachelor Degree
Science & Research Healthcare Life Sciences

Posted 3 weeks ago

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Excellent 4.7

Job summary

Lead multiple routine pharmaceutical studies including release, stability, and quality control by managing testing, data evaluation, report writing, and client communication in a GMP-regulated analytical laboratory.

Responsibilities

The Study Lead manages routine projects including release, stability, and quality control while ensuring adherence to GMP standards and regulatory requirements. They are responsible for communicating project status to stakeholders, mentoring laboratory staff, and overseeing data integrity and technical documentation.

Qualifications

analytical testing data collection software GMP environment HPLC method development protocol preparation scientific report writing study design troubleshooting

Candidates must hold a Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, or a related field. A minimum of 5 years of relevant industry experience with strong hands-on expertise in HPLC and GMP-regulated environments is required.

English

Benefits

  • Immigration and visa support
  • Tax consultations
  • Destination services

Company

Thermo Fisher Scientific

Thermo Fisher Scientific

linkedin
Biotechnology Research
Location
Athlone, Leinster, Ireland

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Excellent 4.7
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