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Scientist – Analytical Development
| Company | Revance |
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| Location | Newark, CA, USA |
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| Salary | $117875 – $147315 |
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| Type | Full-Time |
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| Degrees | Master’s, PhD |
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| Experience Level | Senior |
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Requirements
- Master’s degree in biological sciences or related field with 5+ years or PhD with 2+ years of progressive experience in the biotechnology or pharmaceutical industry.
- Extensive experience performing basic analytical assay techniques such as absorbance assays, chromatography, CE-SDS, ELISA, and western blot.
- Familiarity in interpreting data from common characterization techniques such as AUC, LC/MS, MFI, DLS, and CD.
- Extensive experience developing/authoring protocols, methods, and SOPs.
- Strong written and verbal communication skills.
- Working knowledge of statistics; R, Python, or other statistical tools preferred.
- Ability to work on multiple projects simultaneously, demonstrating organizational and problem-solving skills.
- Self-motivated, proactive and driven individual with an interest in experimental design and development.
- GxP knowledge.
Responsibilities
- Execute technical analytical methodologies to support development and validation of test methods.
- Author and review analytical methods, protocols, reports, and other technical documents, including instrument qualification and change control.
- Operate and maintain (as well as overseeing the installation of) sophisticated analytical instrumentation and associated computer control systems.
- Be part of a team that establishes, maintains, and improves technical operations and project outcomes in the Analytical Development area.
- Provide support for laboratory operations – inventory tracking, reagent preparation, sample management, and documentation review.
- Execute analytical and biological methods ensuring compliance with applicable ICH guidelines and global regulations.
- Ensure adherence to GMPs, GLPs, GCPs and GDPs where required.
Preferred Qualifications
- Expert level experience in Liquid Chromatography and Immunoassays is highly desired.
- Experience in performing change control, deviation, laboratory investigation, and/or other quality records.
- Experience in drafting protocols, methods, and/or procedures.
- Experience or working knowledge in neurotoxin as therapeutics.
