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Great companies hire great people.
In a world of high technology, cutting-edge instrumentation and expensive equipment we believe that our greatest resources are our
people. We recognize that you are entrusting us to carry out your projects in a professional manner. We think that the employees of
ENCO Pharmaceutical Development are highly professional committed and dedicated to a successful conclusion to your projects.
We invite you to take a moment and learn a little about some of our
Scientists, Managers and other key employees.
Trista Dorminey (Materials Manager)
Trista has 9 years of experience in the pharmaceutical and medical device industry including a significant amount of laboratory management
experience. She has extensive experience with stability studies, USP compendia and release testing and method development, validation and
transfers. The Materials group is responsible for a wide variety of analytical chemistry bench testing including compendia methods and wet
chemistry. In addition, this group performs specialized testing on various medical devices.
Anthony Truitt (Chromatography Manager)
Anthony brings more than 15 years of experience in a broad range of analytical and chromatographic
techniques. In addition to his extensive experience in developing chromatographic and trace
analytical methods he also has significant experience with a variety of spectroscopic systems
including GC/MS and LC/MS/MS. The Chromatography group is responsible for all method development
work and those projects of a research nature.
John Faison (QA Manager)
John has 24 years of QA experience in regulated industries. He is a member of the American Society for Quality (ASQ) where he holds a Quality
Auditor certification. He has held leadership positions in the local chapter of ASQ and holds a Six Sigma Greenbelt. The QA group is responsible
for ensuring that ENCO maintains a high quality of compliance with a variety of regulatory agencies. The group also works with our customers during
audits and throughout projects to assist with any compliance topics.
Christy Jones (Customer Service Manager)
Christy has been with ENCO for 8 years in both laboratory and customer service positions including 4 years in laboratory management. She has extensive
experience in the area of customer service and is the company's in-sourcing specialist. She also oversees the customer information section of the
LIMS system. The Customer Services group is the primary company contact for all non-technical issues. This group is an important asset for our customers
during the course of their projects and is focused on providing the highest levels of service.
Kimberley Ashmore (Quality Assurance Manager)
Kimberley is a Quality Assurance professional with 16 years of pharmaceutical GMP experience in contract and generic manufacturing
environments. She has developed quality systems processes, including deviation reporting and resolution, change control management,
and training execution and documentation and has translated paper based quality systems to electronic quality management systems
(such as TrackWise and Agile). The QA group is responsible for assuring the compliance of EPDI systems and processes to the criteria
set forth by current Good Manufacturing Practices and other industry standards.
Dave Heilman (Formulation Development Manager)
Dave has 17 years of experience in pharmaceutical industry in formulating peptides and small molecules for parenteral and topical
delivery. He has several patents for the delivery of anti-HIV peptides to include sustained release formulations using biodegradable
polymer in situ forming implants and microsphere. His background also includes formulation development of nanoparticle systems such as
lyposomes and nanospheres. Dave also has experience in lyophilization cycle development and scale up and tech transfer of manufacturing
processes from lab to production scale manufacturing. Dave has prepared documents for regulatory agencies in the US, EU and Japan.
Gary Strickland (Stability Manager)
Gary has 12 years of experience in pharmaceutical and industrial laboratories including extensive experience with pharmaceutical method
development, analytical method validation, process development and process validation. He has designed developmental stability studies
for formulators to provide stability indicating product performance data for a variety of pharmaceutical dosage forms. Once through the
development process, Gary has experience designing validation and commercial stability studies to satisfy regulatory requirements and
provide product performance data throughout a product’s expiry. Gary is experienced in statistical evaluations of analytical data to
identify and quantify overall product performance.
Christopher Walker (Laboratory Manager)
Christopher brings more than 20 years of experience in the area of analytical chemistry including 15 years in technical management
in the pharmaceutical industry. Christopher has extensive knowledge of analytical techniques used to determine potency, purity and to
characterize small molecules. He has managed analytical sciences support for pharmaceutical development for pre-clinical through NDA
submission, which included analytical support for manufacture, characterization, in-process control, scale-up, reference standards,
and stability studies. As Laboratory Manager, Christopher is responsible for technical, financial, and lab personnel matters for the
RDU facility.
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Why We're Different |
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Discovering Solutions...Delivering Excellence
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