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Principal Specialist, Analytical Method Validation Job Opening In Athens – Now Hiring Lancesoft


Job description

Shift: Normal 9 am 5 pm, no shift work



Duties:

Write analytical method validation protocol in compliance with all applicable FDA/EU/USDA regulations as well as corporate procedures

Provide oversight of validation project and coordinate with laboratory experimental test execution

Summarize laboratory validation test results in validation report

Collaborate with the area manager(s) for project management, project timelines, regulatory documentation and final reports for submission to the USDA



Skills:

Experience with analytical method validation and regulatory method validation requirements (USDA, ICH, FDA)

Preferred experience in writing change controls and conducting impact assessments

Preferred experience with Indirect Fluorescent Antibody (IFA) Test methodology

Working knowledge and basic theoretical understanding of scientific principles (e.G. Microbiology, biological chemistry, biochemistry)

Laboratory and/or Production facility experience preferred

Basic knowledge of pharmaceutical quality

Comprehension of Good Laboratory or Manufacturing Practice (GLP/GMP) and other applicable regulations

Written and verbal communications of technical information



Education:

Bachelor's degree in relevant scientific discipline (e.G. Biology, Microbiology, Chemistry, Biochemistry)

Required Skill Profession

Life Scientists


  • Job Details

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Unlock Your Principal Specialist Potential: Insight & Career Growth Guide


Real-time Principal Specialist Jobs Trends (Graphical Representation)

Explore profound insights with Expertini's real-time, in-depth analysis, showcased through the graph here. Uncover the dynamic job market trends for Principal Specialist in Athens, United States, highlighting market share and opportunities for professionals in Principal Specialist roles.

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Are You Looking for Principal Specialist, Analytical Method Validation Job?

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