Crystal Shrader is a high-skilled professional, working in Lonza as a Compliance Manager from 2016. Crystal Shrader has earned professional experience in more than five positions at various companies. Crystal Shrader went to the The University of Georgia and received education there from 2016 to 2017. Greenwood, South Carolina is the city, where this person was lastly known to be located. This professional's email address and phone number can be easily accessed through SoftwareOfficial on demand.
Name variants:
Chrystal Shrader,
Crys Shrader,
Chris Shrader
Last updated Jul 08, 2024
Contact Information
Last Update
Jun 27, 2022
Email
cr**@lonza.com, cm**@aol.com, cr**@capsugel.com
Location
Greenwood, SC
Company
Lonza
Workplace
Compliance Manager
Work History
Regulatory and Compliance Specialist
412 Mount Kemble Ave SUITE 200S, Morristown, NJ 07960
Capsugel is a global leader in delivering high-quality, innovative dosage forms and solutions to its customers in the health care industry. The company's Hard Capsule business offers custome...
Apr 1, 2014 — Jul 2016
Dea Coordinator
3708 St Elmo Ave, Chattanooga, TN
Served as contact with appropriate federal, state, and local regulatory bodies. Ensured compliance with DEA and state licensing regulations. Prepared and updated mandated reports such as ARC...
Sep 2012 — Apr 2014
Interium Assistant Manager of Quality Control
3708 St Elmo Ave, Chattanooga, TN
Assisted in planning and coordination of ensuring production is continuous and service is consistent with the established standards of quality control program. Plans, promotes, and organizes...
Feb 2012 — Sep 2012
Quality Control Chemist
3708 St Elmo Ave, Chattanooga, TN
Utilized operational knowledge of analytical instruments such as HPLC, GC, FTIR, UV-VIS and data stations to physically and chemically test characteristics of raw materials, production inter...
Apr 2009 — Feb 2012
Education
2016 — 2017
2002 — 2007
2001 — 2005
Occupations
Executive
Compliance Manager
Compliance Agent
Leader
Compliance Officer
Managers
Skills
Pharmaceutical Industry
Fda
Gmp
Validation
Sop
Quality Assurance
Quality System
Capa
Regulatory Affairs
Documentation
Manufacturing
Biotechnology
21 Cfr Part 11
Laboratory
Process Improvement
Customer Service
Regulatory Compliance
Research
Project Management