Director, Oligonucleotide Manufacturing & Process Innovation
Eurofins Genomics Americas
Louisville (KY)
Vor Ort
USD 180.000 - 240.000
Vollzeit
14 Tage+
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Benefits dieser Stelle
Comprehensive medical coverage
401(k) with company match
Paid vacation and holidays
Zusammenfassung
A biotechnology firm located in Louisville, KY is seeking a Director of Oligonucleotide Manufacturing. This role involves overseeing daily operations of the oligonucleotide synthesis facility, leading a team of 40-50 employees. Candidates should have significant experience in manufacturing operations, process optimization, and automation, as well as a strong background in organic chemistry. The ideal applicant will possess exceptional leadership skills and a commitment to quality and regulatory compliance. Comprehensive benefits and a full-time employment status are offered.
Qualifikationen
8-10 years of direct experience in manufacturing operations.
Experience with GMP environments and lean/six sigma methodologies is a plus.
Strong background in oligonucleotide synthesis is advantageous.
Aufgaben
Oversee daily oligonucleotide manufacturing operations for quality and efficiency.
Drive Lean and Six Sigma projects for continuous improvement.
Collaborate with teams for new product introduction and enhancements.
Develop process controls and performance metrics for quality compliance.
Kenntnisse
Operational efficiency
Continuous improvement initiatives
Manufacturing operations
Organic chemistry
Interpersonal and communication skills
Ausbildung
Bachelor's degree in a scientific or engineering discipline
MS or PhD in Organic Chemistry or a related field
Jobbeschreibung
A biotechnology firm located in Louisville, KY is seeking a Director of Oligonucleotide Manufacturing. This role involves overseeing daily operations of the oligonucleotide synthesis facility, leading a team of 40-50 employees. Candidates should have significant experience in manufacturing operations, process optimization, and automation, as well as a strong background in organic chemistry. The ideal applicant will possess exceptional leadership skills and a commitment to quality and regulatory compliance. Comprehensive benefits and a full-time employment status are offered.
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