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Denise Seitz, has over 8 years of GLP/GMP pharmaceutical industry experience.
She began her career as a Document Admin/Technical Writer at Siegfried (USA),
where she was responsible for managing all aspects of the Quality Analytical
Services that provided assistance and support to both the Quality Control and
Analytical Development Laboratories. Her responsibilities included preparation
of detailed professional reports, compiling and editing analytical methods and
monographs, and developing and managing the department library, database and
files. In addition, she wrote and tracked documents such as Standard Operating
Procedures (SOP's) and Certificate of Analysis (COA's). In this role, she also
initiated and implemented Management of Change (MOC's) and trained office
assistants. She honed her organizational skills in maintaining filing systems
and in acting as the main contact for purchasing and billing of all laboratory
supplies and chemicals. Denise has also worked as the liaison between Quality
Assurance and Regulatory Affairs which increased her GLP and GMP document
management skills.
Prior to coming to Critical Path Services, Denise worked for E-A-R Specialty
Composites as an Administrative Assistant/Production and Warehouse Clerk. In
this position, she prepared and recorded reports on volume of production,
consumption of raw material, quality control, and other aspects of production
for the industrial establishment.
Her extensive background and her excellent attention to detail enable Denise to
readily assume her duties at Critical Path Services as an Assistant Sample
Manager.
Denise is currently pursuing her education for an Associate Degree in Applied
Science at Salem Community College. |