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Senior Quality Compliance Specialist

Singapore, Singapore
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At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization. It’s reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines and our BioLife Plasma collection network. When you’re a part of our team, you’ll do meaningful work that makes an impact on the lives of patients. Learn more about us and explore the opportunities to build a remarkable career.

Job ID R0136708 Date posted 10/28/2024 Location Singapore, Singapore

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Job Description

Company Profile:

Takeda's Singapore biologics manufacturing facility focuses on manufacturing potentially life-saving medicines for patients suffering from rare blood disorders such as Hemophilia A and B. As part of the company’s Biologics Operating Unit network, the site is Takeda’s only biologics drug substance manufacturing facility in Asia.  The facility has two buildings, including manufacturing suites and laboratories, as well as Takeda’s first positive energy building certified by Singapore’s Building and Construction Authority’s Green Mark scheme in 2022.

Job Title: Senior Quality Compliance Specialist
Location: Woodlands, Singapore

About the role:

  • This position is responsible for site quality compliance governance and product quality and compliance communications to achieve the site objectives for Takeda Singapore.

How you will contribute:

Inspection and Audit Management

  • Support to host and manage regulatory inspection and communications.

  • Support and ensure the site is inspection ready at all times.

  • Lead and support the site inspection readiness activities.

  • Lead Auditor to lead the self inspection program and plan for self inspection schedule.

  • To perform supplier qualification which include supplier audit.

Site Quality Compliance Governance

  • Participate and lead Quality System(s) rollout by ensuring that the elements of the assigned Quality System (s) is / are implemented and maintained at the site according to regulatory, corporate and division requirement for Quality Council and Quality Risk Register.
  • Participate in any corporate/division alignment meetings for information learning & sharing and alignment of best practices.
  • Responsible for reporting site KPIs and matrix to the site management.
  • Host and manage monthly Quality Councils meeting.
  • Oversight and manage site Quality Risk Management.

Product Quality and Compliance communications

  • Participate and lead Quality System(s) rollout by ensuring that the elements of the assigned Quality System (s) is / are implemented and maintained at the site according to regulatory, corporate and division requirement for Product Recall Quality.
  • Ensure timely investigation and report for customer complaints and product recall.
  • Coordinate and report product quality issues to health authorities via quality incident management process.

Product Complaints program management

  • Coordinate site product complaints to ensure timely investigation and report for customer complaints and product recall.

Other responsibilities

  • Responsibility to adhere to any applicable EHS requirements.

  • Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda’s Code of Conduct

  • Any other duties as assigned by supervisor.

What you bring to Takeda:

Education and Experience Requirements

  • University degree in Biotechnology, Chemistry, Pharmacy, Science, Engineering or equivalent.

  • At least 5-7 years of experience in Pharmaceutical or related manufacturing environment.

  • Demonstrated ability to collaborate with cross functions or cross sites to achieve objective.

Key Skills and Competencies

  • An ability to interact and communicate with all types of personalities in an effective and diplomatic manner.

  • Ability to create and mediate common understanding and communicate expectations on compliance.

  • Presentation skills for audit, training and Senior Management.

  • Substantial knowledge in regulatory requirements, such as Eudralex, 21CFT, ICH, etc.

  • Able to logically solve problems in order to find timely solutions.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

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 deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

Locations

SGP - Singapore - Woodlands

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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Working at Takeda

  • Inclusion

    Here, you will feel welcomed, respected, and valued as a vital contributor to our global team.
  • Collaboration

    A strong, borderless team, we strive together towards our priorities and inspiring mission.
  • Innovation

    Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.
  • Top Workplace

    Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer® status for 2024.
  • Work-Life

    Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.
  • Empowerment

    Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

What we believe in

Our values of Takeda-ism are Integrity, Fairness, Honesty and Perseverance, with Integrity as the core. These are brought to life through actions based on Patient, Trust, Reputation and Business, in that order.

Our belief in putting people first extends beyond our patients — it includes their families and communities, as well as our Takeda colleagues and their families.

We are committed to embracing our differences, valuing different perspectives, and fostering a culture of respect, inclusiveness and empowerment.

Our embedded Diversity, Equity & Inclusion (DE&I) strategy enables us to attract and retain exceptional talent, drives innovation, and helps address systemic inequalities in our communities.

  • Integrity

  • Fairness

  • Honesty

  • Perseverance

We're Steadfast In Our Commitment to Four Key Imperatives

Patient


Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.

People


Create an exceptional people experience.

Planet


Protect our planet.

Data & Digital


Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.

Exterior of Takeda Building

About our location

Singapore, Singapore


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