| Company: | Larada Sciences |
| Job Location: |
Salt Lake City - Salt Lake County |
| Employment Type: | Full Time |
| Salary Range: | COE |
Description: |
Larada Sciences Inc. is an early stage technology company that develops, manufactures and markets breakthrough medical devices and related services.
We are presently looking for a full-time regulatory affairs/quality assurance specialist to join our Team. The selected individual will be primarily responsible for creating, implementing and managing our regulatory and quality assurance systems.
Please forward resumes to sherrijones@laradasciences.com
|
Duties: |
The successful candidate will be able to wear many hats and tackle a wide range of responsibilities, including the management of design control and other quality systems, manufacturing quality and deviation systems, various compliance and reporting systems, regulatory filings, developing and writing policies and procedures, and working with the Engineering team on various testing, certification and manufacturing issues.
The right individual will join a small team of dynamic, highly motivated individuals in a fast-paced and personally rewarding environment. This is a day shift position based in Salt Lake City, infrequent travel may be required, and compensation is commensurate with experience
|
Qualifications: |
Bachelors Degree /Master’s Degree in a relevant technical program
Minimum 2 year experience in pharmaceutical, biotech and/or medical device industry
Some working knowledge of current Medical Device Design Controls, Good Manufacturing Practices, ISO and FDA regulations and requirements
Good English writing skills, organizational skills and attention to detail
Positive, outgoing personality with good verbal communication skills
Self-starter with ability to work independently
Solid computer skills in the basic office suite programs
Desire and ability to thrive in an entrepreneurial and participative team environment
|
