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Support Quality Assurance Document Control functions, with a specific focus on filing, scanning, organizing, and reviewing GMP records.

Assist with the retention and organization of all GMP documents.
File, scan, and index related GMP documentation.
Retrieve GMP documents in response to requests from all departments.
Maintain and improve document logs and the filing system.
Support intercompany communication and document retrieval requests.
Review GMP records for accuracy and compliance with Standard Operating Procedures (SOPs).
Perform other responsibilities as assigned by the senior leadership team.

High school diploma; some college coursework or an associate degree is a plus.
Previous work experience, preferably in an FDA-regulated industry.
Proficient in using MS Office programs and ERP systems such as Aurantium, and other document management and business communication tools.
Ability to multitask, prioritize and manage time effectively.
Some knowledge of cGMPs related to US FDA and manufacturing environments.
Regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear.
May be required to lift up to 50lbs, stand, bend, climb stairs.
Requires specific vision abilities including close vision and ability to focus.
Requires the ability to climb stairs as part of regular duties, including accessing multi-level facilities or transporting documents between floors.
Must be present in the office to collaborate with peers and supervisors.
Work/Travel schedule must be adhered to and/or changed as needed to meet business requirements.
Potential ongoing travel throughout geographic areas on a continual basis as normal scope of role.
Personnel Protective Equipment or Attire Required for Position: As needed.

Administrative Assistant; QA Document Control at CONTRACT PHARMACAL CORP

Administrative Assistant; QA Document Control