Work history

Eurand October 2002 to the present
Compliance Manager

tags:

How would you describe your time at Eurand?

Responsible for all GMP regulatory compliance activities in support of the manufacture of solid oral dosage pharmaceutics.
Alkermes January 2002 to October 2002
QA Auditor IV

tags:

How would you describe your time at Alkermes?

Responsible for batch record and associated documentation review to determine batch disposition.
MacroMed May 2001 to January 2002
Documentation Specialist

tags:

How would you describe your time at MacroMed?

Responsible for designing and implementing a document control system and all associated quality system documentation.
Pharmadigm April 2000 to April 2001
QA/RA Specialist

tags:

How would you describe your time at Pharmadigm?

Responsible for preparation of all IND regulatory submissions and QA support of contract manufacturing.
Watson Laboratories August 1995 to April 2000
Technical Writer

tags:

How would you describe your time at Watson Laboratories?

Responsible for all aspects of stability testing and reporting in the R&D department. Raw material group leader in Quality Control. Preparation of CMC sections for all IND/NDA submissions.

Education

Utah State University March 1988 to May 1995
Biology

tags:

How would you describe your time at Utah State University?

Obtained B.S. in Biology with a Chemistry Minor.

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