Documentation Specialist

1 week ago


Singapur, Singapore Takeda Full time
About the Role

We are seeking a highly skilled Documentation Specialist to join our team at Takeda's Singapore biologics manufacturing facility. As a key member of our documentation team, you will be responsible for providing full documentation support to Manufacturing, maintaining administrative systems, and ensuring compliance with regulatory requirements.

Key Responsibilities
  • Provide documentation support for manufacturing processes, including preparation and issuance of MBR/MFR packages, reconciliation of ECC forms, and data interface with PRIMR.
  • Maintain administrative systems, including SOPs, Forms, and TQs, and ensure compliance with regulatory requirements.
  • Collaborate closely with other departments to resolve issues related to daily operations and support continuous improvement initiatives.
  • Develop and maintain personal development plan and provide annual performance self-assessment.
Requirements
  • Minimum Diploma with 2-4 years of relevant experience in Pharmaceutical/Manufacturing environment or related fields.
  • Effective interpersonal, organization, and communication skills, and the ability to work in a multi-disciplinary team.
  • Team player, self-driven, and able to work under pressure with a sense of urgency.
  • Experience in PRIMR/JDE or equivalent system will be an added advantage.
About Takeda

Takeda is a patient-focused company that inspires and empowers its employees to grow through life-changing work. We are committed to delivering Better Health and a Brighter Future to people around the world.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to our mission.



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