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Sr. Scientist – Analytical Development
| Company | Revance |
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| Location | Newark, CA, USA |
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| Salary | $135470 – $169395 |
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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
- Ph.D. degree in biological sciences or related field with 5+ years of progressive experience in the biotechnology or pharmaceutical industry. (Candidates with M.S. with extensive experience may be considered.)
- Extensive experience performing basic analytical assay techniques: absorbance assays, SDS-PAGE, chromatography, CE-SDS, ELISA, western blot, cell-based potency assay.
- Extensive experience in common characterization techniques such as AUC, LC/MS, MFI, DLS, and CD.
- Extensive experience developing/authoring protocols, methods, and SOPs.
- Be able to communicate technically and strategically across technical and operational activities and work collaboratively to ensure successful execution.
- Strong written and verbal communication skills.
- Working knowledge of statistics; R, Python, or other statistical tools.
- 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.
- Operation, maintenance, and 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 for LC-MS/MS is highly desired.
- Experience in extended characterization (such as AUC, SEC-MALS, DLS, Peptide Mapping) is highly desirable.
- Experience in drafting protocols, methods, and/or procedures.
- Experience or working knowledge in neurotoxin as therapeutics.
- Experience in performing change control, deviation, laboratory investigation, and/or other quality records.
