5 years biotechnology or pharmaceutical experience
Strong understanding of cgmp regulations
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Merck & Co., Inc. is seeking an Associate Technical Specialist in Quality Control at their Dunboyne, Ireland facility. The role involves providing technical expertise in quality control testing, method execution, and team leadership within a biologics drug substance commercialisation environment.
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Job Summary
This role involves developing and coaching the Quality Control team while driving a high-performance organizational culture.
The position requires performing advanced assays and supporting regulatory submissions and health authority inspections.
Candidates must maintain data integrity and ensure compliance with FDA and cGMP regulations in a dynamic commercialization facility.
Matching Summary
Match Score: 75
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Merck & Co., Inc. is seeking an Associate Technical Specialist in Quality Control at their Dunboyne, Ireland facility. The role involves providing technical expertise in quality control testing, method execution, and team leadership within a biologics drug substance commercialisation environment.
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Skills & Requirements
Must-have
Master's degree in Science or Quality discipline
5 years biotechnology or pharmaceutical experience
Strong understanding of cGMP regulations
Expertise in ELISA, SDS-Page, Bio-Assays, PCR
Experience with analytical method development and validation
Nice-to-have
Lean Six Sigma experience
Leadership skills managing daily activities
Continuous improvement tools like DMAIC or 5S
Ability to work on own initiative
Excellent written and oral communication skills
Key Requirements
Master's degree with 5 years experience OR PhD with 3 years
No VISA Sponsorship available
No relocation assistance provided
Must have strong biochemical and cell biology methodology knowledge