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Company Overview:
Synergy Bioscience, a pharmaceutical contract research organization (CRO), provides product development, analytical chemistry, microbiology testing, as well as quality compliance consulting services to the FDA-regulated companies. We are currently seeking highly qualified R&D scientists with extensive experience in pharmaceutical product development, instrumental analysis, writing technical reports and strong working knowledge of GC-MS.
Role and Responsibilities:
The successful candidate will have knowledge in GC-MS, protocol writing, technical writing, FDA regulation, GMP, GDP and a Team Player. They will analyze results, interpret data, and provide both oral updates and written reports in collaboration with the laboratory manager. Adherence to Standard Operating Procedures (SOPs), safety guidelines, and compliance with current Good Manufacturing Practices (cGMP) regulations will be required in this highly regulated work environment. The individual will also ensure that the R&D lab remains a GMP-compliant and safe working environment.
Key responsibilities include:
Qualifications and Experience:
Skills Required:
Full Time
$53k-68k (estimate)
06/27/2024
08/26/2024
synergybioscience.com
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