Manufacturing and Supply Where the miracles of science are made a reality for patients
About the Job
The Quality Systems and Compliance sub-team is under the remit of the Site Quality Department and is responsible for the quality system management (QMS) implementation within the site. The team is responsible for setting up or reviewing and auditing the quality management systems, third party and supplier management system, Training and Documentation systems to be used by the entire site, which is instrumental in ensuring the site systems and processes meet the international GxP requirements. The team is also responsible for the Data Integrity (DI) Program to ensure the compliance use of the digital initiatives. This includes working closely with the respective functional teams to provide oversight and guidance for data integrity and projects related to data integrity to achieve the site’s digital ambition while in compliance with data integrity requirements. Another aspect is to manage Quality Culture program, enabling the right Quality Culture to be embedded onsite.
Documentation Management System:
Support the implementation of digital documentation solutions like electronic logbooks and manage the GMP governance and issuance of paper-bound logbooks on site.
Support the implementation of digital documentation solutions like electronic forms and manage the GMP governance and issuance of controlled printing of forms on site.
Lead and implement framework and solution for document archival and destruction process on site.
Quality Culture Program/ Data Integrity:
Support in the development and roll out the Quality Culture program onsite
Tracking of Quality gaps and near misses, with the use of data visualization tool to communicate stakeholders
Status tracking of identified actions in Data Integrity Plan
Site Inspection Readiness and Management
Provide support for logistics activities for internal and external inspections. Provide support for site inspection readiness program.
Quality Projects
Status tracking of Site Quality Projects.
Provide support for identified site Quality Projects.
About You
Degree or Diploma preferably in a related field
Previous internship or work experience in any fields
Candidates from Polytechnic or University programmes are welcome to apply
Strong organizational and time management skills with the ability to manage multiple tasks simultaneously
Excellent written and verbal communication skills
Pursue Progress . Discover Extraordinary .
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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11000 - 14000 SGD
...Takeda's Singapore biologics manufacturing facility focuses on manufacturing... ...life-saving medicines for patients suffering from rare blood... ...to manage the Manufacturing Sciences Laboratory within the approved... ...technologies within the laboratory where applicable, apply these...
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