In addition to the 7 postings already in UMBCworks, Wyeth Pharmaceuticals has just announced another opening for an intern in the Compendial Affairs Office of their Global Regulatory Affairs Division. Position details are below. To apply for this position or any other internship with Wyeth, submit your resume to UMBCworks or email it to Kerry Kidwell-Slak in the Shriver Center at kerryk@umbc.edu.
RESUME SUBMISSION DEADLINE: February 6, 2009
Project Title(s): Project Manager/Compendial Coordinator
Project Description(s): [Non-Lab position] Facilitate meetings, review & refine process for data collection of US, European, and Japanese standards impacting product portfolio; calculate metrics of responses received from individual sites for each business unit, prepare reports, explore data system and search engines to optimize the data output, link individual data from multiple spreadsheets to a collective repository for final report generation.
Educational requirements(s): Pre-medicine, Pre-Pharmacy, Nursing, Biology, Chemistry, Project management, Computer science/programming
Desirable experience: Familiar with Microsoft Office with emphasis in Excel and Access programs. Candidate should have ability to learn new computer system operations quickly. Understanding of medical terminology and product formulation information desired.
Benefits to the Intern: This position will provide an understanding of regulatory and compendial compliance requirements applied within a Pharmaceutical company. Intern will learn communication skills, experience team environments, work with a diverse culture, have exposure to regulatory guidelines, and pharmacopoeia* standards. The position will work with various computer systems & Microsoft programs to optimize the data collection, upload information to a central repository, and generate final reports.
*Pharmacopoeias are publication of core methods, test procedures, acceptance criteria and general guidelines that reflect standards for determining the quality of manufactured medicines