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RssClinical Regulatory Affairs

I am a certified PMP Project Manager with 19 years of project manager experience; the bulk of my career is in software development.    Most recently, I worked at Alcon Labs as a development manager where I was responsible for managing the daily activities of 5 software developers and 2 verification engineers; managing the development of up to 14 software projects simultaneously; and functionally managing a group of 15 software developers.  Due to company restructuring, 100 positions including mine have been eliminated. Prior to Alcon, I was a software development manager that managed the daily activities of 5 software developers, performed requirements analysis, developed software architectures, wrote user manuals, and created software prototypes to insure a higher rate of user acceptable. I find that wherever I have worked I bring three key strengths to the table: team development skills, meeting commitments on time, and developing processes to increase productivity and product quality. At this time, I am looking for a management position in an organization that values high quality software created using the most effective engineering methods.

Clinical Regulatory Affairs

Dexter, MI

About Me


Science & Biotech


Clinical Regulatory Affairs

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Dexter, MI