AbbVie Document Control Supervisor in Singapore, Singapore

Description:
* Implement and maintain a documentation change control system following approved procedures and in compliance with GMP and data integrity requirements * Coordinate with other QA section personnel and appropriate representatives from other departments to assure compliance with GMP on all documentation * Ensure that document changes are verified for completeness accuracy and meeting AbbVie requirements (i.e. specifications, batch records, operating procedures) * Maintain compliance with AbbVie Documentation System ensuring Document Control Specialist is trained in appropriate procedures * Assures all controlled quality system documents are retained and destroyed according to AbbVie policies, process and procedures * Responsible to secure and control Site Record Retention Room(s) * Ensure Documentation Control provide compliant, on-time document process and control services while maintaining a customer satisfaction service level * Report metrics to site management on established basis * Conduct investigations for documentation processing related events involved with Documentation Centre * Review proposed site specific changes or global document changes from Center of Excellence teams and provide feedback to assure that site complies with requirements of these Global policies when implemented * Supervise Document Control Specialists in the area * Assured that employees’ growth plan and developmental plan are updated on a yearly basis or as needed * Promote and follow safety work practices in the workplace

Qualifications:
* Master or Degree in Sciences, Biology, Chemistry, Pharmacy, Engineering or equivalent. * Minimum 4 years of relevant experience in quality/compliance (GxP) environment, with 2 years of experience leading a team. * Preferably familiar with regulations and standards in area of API and Biologics. * Ability to quickly know products and processes in order to assess quality issues * Demonstrates the highest levels of integrity and a strong work ethic * Enjoys problem solving and ability to make decisions * Good planning and scheduling skills * Strong communication skills both verbal and written * Driven and good team player * Strong interpersonal skills

Job Classification: Experienced
Job: MANUFACTURING & OPERATIONS
Primary Location: Singapore-Central Singapore-Singapore
Organization: Operations
Schedule: Full-time
Shift: Day
Travel: No
Req ID: 1706169