Quality Systems - Temp
This temporary position is responsible for day to day activities
managing and maintaining the flow of both electronic and hard-copied controlled documents, department files and resource
materials. Incumbent is also responsible for filing and GMP document activities and change administration requirements
for product documentation. In addition, performs process improvement activities within the Document Control Area.
Responsibilities include logging, tracking and maintaining GMP documentation, coordinating document control issues between
departments and preparing repmis regarding quality issues. This position must also be able to maintain confidentiality.
Maintenance of Quality System documents- Master Records, SOP, Annual Product Review,
Area Reference copies, etc. Periodic Review documentation, filing and archiving activities.
Issuance of lot numbered documents and forms for manufacturing, quality control and
other depmiments as needed.
Customer Service Activities -departmental copy requests, internal customer inquiries,
expedition of departmental copy requests.
Perform or delegate other duties or special projects as assigned.
Knowledge of the current Good Manufacturing Practices.
Good verbal, written and organizational skills. The position requires
that the employee communicate with internal groups.
Strong computer skills, Microsoft Office Applications (Access, Excel and Word).
Ability to follow through and consistently demonstrate that all primary job
duties and responsibilities are current and up to date; ability to monitor and communicate progress to Management.
Must be able to work as a team member.
Must be able to work a consistent schedule to satisfy the responsibilities of the job.
Education and Experience:
A minimum of one to three years of quality assurance experience in the pharmaceutical
G & W Labs - 20 months ago