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The Company
Scorpius BioManufacturing is a boutique biologics CDMO providing cGMP manufacturing, bioanalytical, and process development services for protein modalities. Our San Antonio, Texas facility specializes in working with start-ups, emerging biotechs, and academic researchers. Scorpius was founded by a serial biotech entrepreneur determined to make small-volume programs a big priority. Clients benefit from decades of expertise taking large-molecule drugs to market and can rely on Scorpius to offer Quality, Speed, Flexibility, & Responsiveness.
Position Summary
This role will be responsible for the support of GMP compliance with a focus on Manufacturing. The candidate will provide critical review, organization, and Quality oversight of records generated during GMP manufacturing, release, and stability testing of Drug Substances/Drug Products, as well as analytical records. They will make sure that product and manufacturing process records are within the specifications established and include complete information relating to the production and control of each manufacturing lot at Scorpius BioManufacturing.
The ideal candidate must exhibit attention to detail and good time-management skills to adapt with rapid business goals; and be organized, self-motivated, and thrive in a fast-paced and dynamic biotech environment. She/he/they must be versatile and adapt to rapid change with a strong desire to make a significant impact.
Duties and Responsibilities
Required Competencies
Knowledge and Skills
Education & Experience
Physical Requirements and Working Environment
Full Time
$90k-108k (estimate)
04/23/2024
05/09/2024