Reporting to the Sr. Production Manager, the position will fulfill the documentation responsibilities for the Technichal Operations Department of Novartis Animal Health in Larchwood, Iowa. |
The candidate will coordinate and execute quality documentation activities in a timely and effective manner per Novartis Quality procedures and standards and contribute to the overall success of the Quality department.
Responsible for Quality Module maintenance including authorization and Standard Operating Procedure maintenance including formatting and archiving.
Responsible for the filing of product complaints.
Responsible for the labeling control system and e-filing system.
Create and maintain training program related documentation and schedule and coordinate training sessions as required.
Oversee the change control system including database maintenance
Bachelors degree or equivalent.
Knowledge/familiarity of basic GMP compliance.
Strong project management skills.
Effective interpersonal skills.
Ability to effectively communicate verbally and in writing.
Strong leadership skills.
Ability to effectively work with teams.
Ability to set priorities and manage multiple tasks effectively.
Novartis - 23 months ago
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Novartis AG, incorporated on February 29, 1996, is a Switzerland-based holding that, through its subsidiaries, is engaged in the research,...