Job Description
Overview of the Quality Department:
The Quality Department is integral to ensuring that our biopharmaceutical products meet the highest standards of safety, efficacy, and compliance. The department is divided into several specialized areas, each focusing on a critical aspect of quality management. These include Quality Control, Quality Operations, Quality Assurance, Quality Compliance, and Quality Services Improvement. Our team is dedicated to continuous improvement and innovation, leveraging cross-functional collaboration to drive excellence in all our processes.
Responsibilities:
Quality Control Department:
- Raw Material Lab: Assist with daily operational activities, including water testing.
- Lab Services: Support day shift operations and handle administrative duties for medically unfit colleagues.
- Micro Lab: Participate in daily environmental sampling during day shifts.
Quality Operations and Quality Assurance Support:
- Quality Operations: Review manufacturing batch records.
- Quality Assurance Support: Support incoming receiving and archival activities, along with other administrative responsibilities.
Quality Compliance Department:
- Assist with inspection activities.
- Contribute to identifying process improvements to streamline inspection readiness and follow-up actions.
Quality Services Improvement Department:
- Aid in deploying Continuous Improvement initiatives.
- Collaborate on cross-functional projects like digital transformation (e.g., Power BI) to enhance efficiency and innovation.
- Coordinate logistics for training programs and engagement events.
- Implement and maintain the Quality Communications Blueprint, managing platforms like the Quality intranet and Townhalls.
Key Skills and Competencies:
- Committed to the role assigned.
- Positive mindset and motivated.
- Able to understand constraints at times and be flexible.
- Good interpersonal, verbal, and written communication skills required.
- Ability to work and collaborate within the team.
- Good time management skills.
- Keen interest to work in a biopharmaceutical industry.
- Knowledge and experience using Microsoft Office.
Locations
SGP - Singapore - Woodlands
Worker Type
Employee
Worker Sub-Type
Fixed Term (Fixed Term)
Time Type
Full time
Top Skills
What the Team is Saying
What We Do
For over 240 years, Takeda’s propensity to evolve has driven the next generation of innovation, and as a future-focused organization, we’re continuing to drive forward with endurance in our steadfast pursuit to achieve the best outcomes for our patients in a rapidly changing world.
We have been preparing for this period of value creation by investing in data, digital and technology, and we’re proud of our employees and their commitment to turning groundbreaking ideas into life-changing impacts.
Since our founding in Japan, integrity and putting patients first have been at the heart of our identity, and we will emerge ready for our future as one of the most trusted and science-driven digital biopharmaceutical companies. Join a team where your innovation impacts lives.
Together, we’ll realize improved outcomes by improving data quality, enhancing launch execution and improving the patient journey. You’ll play a critical role in accelerating data collection and increasing accuracy across all parts of the business. Patients across the globe will benefit from access to treatments afforded by greater opportunities and efficiency in our research and development.
Why Work With Us
We connect to our history and Japanese heritage through everything we do to bring our purpose, values, vision, and imperatives to life. We are committed to bringing better health and a brighter future to patients. Being a part of Takeda means having the opportunity to be a part of something bigger than yourself.
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Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Takeda's hybrid policy varies by role. Be sure to ask your recruiter about the requirements for the role that you are applying for.
