Job Search Results - Biospace
Get Our FREE Industry eNewsletter


Refine Job Search:

Clear All Selections
Selected Employer
Revance Therapeutics, Inc.

Clear All Selections

Your search returned 7 jobs



2/15/2017
Revance Therapeutics, Inc.
Newark, CA

The Regulatory Affairs Associate II prepares and submits high quality routine regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. They will also support the...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

Responsible for quality oversight of validation efforts supporting computerized systems, equipment and instruments. This position is also responsible for business administration support of Quality applications. Essential Functions: • Provides QA...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

Oversees and directs the development, planning, implementation and maintenance of manufacturing methods, processes and operations for new or existing products and technologies. Works closely with quality groups to ensure strict compliance with good...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

Lead Analytical group to develop product specific assays for the routine testing and characterization of Revance products. Train QC personnel on new methodologies and participate in the transfer and qualification of these methods. Participate in...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

The Scientist/Senior Scientist, Purification Process Development will be responsible for leading the scientific studies for development, optimization and characterization of purification process of Revance's protein biologic compounds. This...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

Provides strategic direction for QC analytical and microbiology testing, environmental monitoring and assay qualification/validation. Develops, implements and maintains the activities of quality control systems. Oversees quality control operations...

2/15/2017
Revance Therapeutics, Inc.
Newark, CA

You will be a part of the manufacturing organization and provide hands-on execution of tasks related to the cGMP manufacture of biopharmaceuticals working in bacterial fermentation, purification and/or fill-finish. As a lead you set a positive...