HPLC/GC Expert (Eugene, OR)
About The Position
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. This is a six-week contract, beginning in mid-September. We're looking for someone who can help do/lead analytical development to support their synthetic team for the next month and a half. This candidate will need to be experienced with both HPLC development of methods to support small molecule API manufacturing and the qualification/validation of those methods.
Requirements
- 7+ years of experience in small molecule pharma QC or analytical method development.
- Experienced with HPLC method development for small molecule API manufacturing.
- Experienced with qualification and validation of HPLC methods.
Responsibilities
- Lead analytical development to support a synthetic team.
- Develop HPLC methods to support small molecule API manufacturing.
- Qualify and validate HPLC methods.
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What This Job Offers
Career Level
Senior
Education Level
No Education Listed
