► MNC, Manufacturing Industry
► Office Hour
► Working Location: Buona Vista
► 1 year contract
Working with suppliers, internal stakeholder and maintenance of information for both compliance and management purposes
Maintaining supplier profiles in the relevant data systems per procedures
Preparing, communicating/ negotiating, putting in place and maintaining Quality Agreement documentation for suppliers as required
Generating relevant metrics, data analytics and trending for performance management
Interfacing with internal and external stakeholders such as Site Quality, Procurement, SQ Audit, SQ Operations and suppliers – a two-way communication regarding Quality Agreement documents
Proficient influencing and negotiating skills to ensure putting in place Quality Agreement documents while maintaining a good relationship with the supplier.
Ability to work in a structured and methodical manner in order to track, manage and coordinate a significant number of Quality Agreement documents in various stages of progress at the same time with similar deadlines/ priority.
Good time management skills to ensure assigned activities and associated documentation are completed within the required timelines.
Ability and willingness to maintain rapid response to customers, staff and management.
Demonstrated ability to function effectively across multiple cultures and geographic boundaries.
Awareness and understanding of local and global pharmaceutical quality regulatory requirements.
Strong excel skills.
Graduate of Science, Pharmacy, Engineering and/ or prior pharmaceutical quality experience preferred