• The incumbent will prepare analytical, formulation, stability, manufacturing, operating procedures and other technical and GMP related documentation.
• Use Electronic Document Management System (EDMS) for the preparation and maintenance of electronic (documents) records.
• Administer the electronic document review and approval process.
• All work is to be done in a compliant manner according to SOP guidelines and cGMPs.
• The incumbent will review for accuracy, readability and format ensuring that all documents are in compliance with company policies/guidelines and meet the required timelines.
• This position will also maintain hard copy files, electronic data, and records for Consumer Global R&D and enter data in electronic database for data tracking purposes in support of Training department.
• Responsible for performing essential functions of record operations, such as indexing, filing, retrieving, distributing (via copying or check-out), and ensuring the integrity of records housed in the PR&D site repository.
• The individual also participates in various operations, such as annual file review, relocation of records, inventory control, etc., as required.
• The individual assists with other QC&C clerical activities, as required