Product Transfer Scientist Astute Medical, Inc.
THIS JOB HAS EXPIRED Job ID#: 55108
Astute Medical, Inc., start-up in vitro diagnostic company, is seeking a motivated and detail-oriented scientist to lead and coordinate product transfer activities. This position will work closely with technical and nontechnical departments throughout the company to guide the transfer of product designs and improvements from a development setting to a final manufacturing environment. This is a contract position with an expected duration of 6 months.
Actively participate in the development of new products and product improvements as a technical liaison between R&D, Engineering, and Manufacturing organizations. Partner with these organizations to ensure efficient, thorough, and accurate transfer of new product designs to routine production.
As appropriate, provide technical input to other departments with regard to production and development activities such as:
o Product Labeling
o Product Packaging
o Product risk analysis
Lead, coordinate, or participate in activities required for the transfer of new products to routine production such as:
o Raw material sourcing
o Scale-up of manufacturing processes
o Process development / optimization / transfer
o Technology transfer
o Process / Equipment / Test Method Validation
Develop and maintain documentation related to product design, design change and transfer such as:
o Design specifications
o Product change orders
o Manufacturing procedures / SOP?s
o Production flow charts
o Production metrics
o Study reports
Proactively identifies both technical and non-technical problems. Leads and / or participates in problem solving efforts.
Minimum of 5 years of development, manufacturing, and / or other relevant experience in the in-vitro diagnostics, medical device, and / or related industries.
Demonstrated knowledge of design controls or other product development / commercialization processes for in-vitro diagnostics or medical device products.
Ability to work effectively with cross-functional core teams as well as external corporate partners. Experience working with external contract manufacturing organizations preferred.
Detail-oriented. Ability to multi-task effectively.
Ability to work within a regulated environment. Familiar with US and EU medical device regulations.
Ph.D. in chemical sciences, life sciences, engineering, or other relevant discipline preferred.
Please email or fax your resume or curriculum vitae to us at the address below. Be sure to specify job reference ID# 55108 in the subject of the message.
||San Diego, CA |
THIS JOB HAS EXPIRED