Summary:

Responsible for administration of the validated Learning Management System (LMS) including but not limited to evaluating and managing functionality of the system data, ensuring system accuracy of completions, revisions, notifications, and reporting. The Training Administrator supports end users of the Grifols training platform.

Knowledge, Skills and Abilities:

Knowledge of cGMPs, FDA regulations, and industry guidelines, as well as international regulatory guidelines. Ability to keep neat, accurate and complete records and logs, preferably experienced in working with training databases. 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. Strong organizational, analytical, troubleshooting, and problem-solving skills. Ability to analyze details and perform structured decision-making daily. Excellent verbal and written communication. Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner. Good computer skills with knowledge of MS Office, particularly Word, and PowerPoint. Intermediate or Advanced Excel experience is preferred. Manual dexterity to perform clerical type functions such as typing, using a mouse, copying, faxing, etc. Ability to work at a computer and view video display terminal less than 18” away from face for extended periods - up to four (4) hours at a time. Ability to read and review documents for extended periods - up to four (4) hours at a time. Ability to stand or sit for extended periods - up to four (4) hours at a time. Ability to lift and/or move up to 50 pounds. Ability to gown and enter an aseptic, cold (65˚F) environment.

Education and Experience:

Minimum of High School Diploma or GED. Minimum 3 to 5 years of experience preferably in an FDA regulated manufacturing facility– pharmaceutical, biologics, biotech, or medical device industry.

Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Occasionally walks and stands. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues.

EEO Females/Minorities

Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton

Learn more about Grifols