Quality Compliance Specialist

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.

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

1. 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 forself inspection schedule.

. To perform supplier qualification which include supplier audit.

2. Site Quality Compliance Governance

. Participate and lead Quality System(s) rollout by ensuring thatthe elements of the assigned Quality System (s) is / are implemented andmaintained at the site according to regulatory, corporate and divisionrequirement for Quality Council and Quality Risk Register.

. Participate in any corporate/division alignment meetings forinformation learning & sharing and alignment of best practices.

. Responsible for reporting site KPIs and matrix to the sitemanagement.

. Host and manage monthly Quality Councils meeting.

. Oversight and manage site Quality Risk Management.

3. Product Quality and Compliance communications

. Participate and lead Quality System(s) rollout by ensuring thatthe elements of the assigned Quality System (s) is / are implemented andmaintained at the site according to regulatory, corporate and divisionrequirement for Product Recall Quality.

. Ensure timely investigation and report for customer complaintsand product recall.

. Coordinate and report product quality issues to healthauthorities via quality incident management process.

What you bring to Takeda:

Education and Experience Requirements

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

. At least 3-5 years of experience in Pharmaceutical or relatedmanufacturing environment.

. Demonstrated ability to collaborate with cross functions orcross sites to achieve objective.

Key Skills and Competencies

. An ability to interact and communicate with all types ofpersonalities in an effective and diplomatic manner.

. Ability to create and mediate common understanding andcommunicate expectations on compliance.

. Presentation skills for audit, training and Senior Management.

. Substantial knowledge in regulatory requirements, such asEudralex, 21CFT, ICH, etc.

. Able to logically solve problems in order to find timelysolutions.

More aboutus:

AtTakeda, we are transforming patient care through the development of novelspecialty pharmaceuticals and best in class patient support programs. Takeda isa patient-focused company that will inspire and empower you to grow throughlife-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.