Director of Research and Development

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Location
South Bend, IN
Salary
$90,000 - $130,000
Job Type
Direct Hire
Degree
Bachelor of Arts, Bachelor of Science
Date
Apr 21, 2017
Job ID
2450782

Company Background

For 30 years, this research laboratory has been manufacturing and distributing a variety of enzymes and cofactors used in basic coagulation research.  They are known and trusted by coagulation communities worldwide for their purified coagulation factors and research reagents. Their sister diagnostics company provides general purpose and specialty assays to the clinical coagulation laboratory. This diagnostics company was organized to incorporate the research laboratories high purity proteins and reagents into clinical diagnostic kits. This diagnostics division seeks an energetic Director of Research and Development with an entrepreneurial attitude and a desire to play an integral role in the growth of the company.

 

Position Overview

The Director of Research and Development is primarily responsible for new product development and technical support to manufacturing and to customers, consistent with the size and growth of the company, and in conjunction with the company Quality Policy and Objectives. 

Position Duties & Responsibilities

·         Determine unmet needs of commercial potential for the clinical coagulation laboratory.

·         Determine product and process essential requirements to meet these unmet needs.

·         Plan, execute, and analyze experimental plans leading to manufacturing formulations and processes for products meeting or exceeding these essential requirements.

·         Coordinate and lead multiple projects in new product development while meeting the requirements of the U.S. FDA and of ISO 13485 for IVDs.

·         Provide technical support to operations and to customers for all existing and future products.

·         Collate and maintain required files and documents which support regulatory submissions.

·         If necessary, prepare and lead PMA and 510(k) filings, Technical File preparation, and CE Marking.

·         In cooperation with other functional managers create, review and approve QS documents to ensure compliance with QSR, ISO and other regulatory requirements. Provide training on these systems/procedures.

·         Initiate corrective and preventive action plans and participate in corrective actions completion by performing root cause analysis and verifying effectiveness.

  

Required Education, Experience, and Characteristics:

·         Bachelor's degree in the natural or life sciences (minimum).

·         Extensive experience and demonstrated success in research, development, and commercialization of clinical coagulation IVD products.

·         Expert knowledge in experimental design and statistical analysis.

·         Expert knowledge of the development process and Design Control, of manufacturing processes, and of clinical laboratory assay design and execution.

·         Demonstrated experience working with ISO, FDA, and other key regulatory bodies within the past 5 years.

·         Ability to communicate at all levels in a diagnostic/manufacturing environment, project management skills, and good interpersonal skills.