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Under the direction of the QA Document Control Supervisor, the QA Specialist Document Control, will control the movement, filing, archiving, and securing of all documents with the objective of ensuring compliance to company policies and procedures. In addition, the QA Specialist will review, issue, and reconcile controlled documents according procedures.
Knowledge and Skills
Must be proactive, results oriented, with a strong attention to detail.
Self-starter with good work ethic and ability to work independently with minimum supervision and use good judgment, or as a contributing member of a team.
Ability to manage multiple projects simultaneously, meet deadlines, and handle an ever changing, fast paced critical work environment.
Excellent verbal and written communication. Must be able to read, write, and speak English.
Good computer skills with basic knowledge of Microsoft programs, particularly Outlook, Word, Excel, etc.
Knowledge of /or SAP (Systems, Applications & Products in Data Processing), MasterControl, Trackwise, is a plus.
Leadership / Managerial Attributes
Strong organizational, troubleshooting and problem-solving skills. Ability to analyze details and perform structured decision-making on a daily basis.
Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
Other requirements (licenses, certifications, specialized training)
Good communications skills
GMP trainer a plus.
Full Time
Pharmaceutical
$71k-89k (estimate)
12/21/2023
06/11/2024
glenmark.com
SAHARGAON, MAHARASHTRA
7,500 - 15,000
2006
$500M - $1B
Pharmaceutical