Vaccine External Supply Quality Lead, Asia
Gurgaon, HaryanaVaccines prevent 2 to 3 million deaths each year and have transformed global public health. For the past 70 years, Takeda has supplied vaccines to protect the health of people in Japan. Today, Takeda's global vaccine business is applying innovation to tackle some of the world's most challenging infectious diseases, such as dengue, COVID-19, Zika and norovirus. Takeda’s team brings an outstanding track record and a wealth of knowledge in vaccine development, manufacturing and global access to advance a pipeline of vaccines to address some of the world's most pressing public health needs.
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Job Description
Job Title: Vaccine External Supply Quality Lead, Asia
Location: Singapore OR Gurgaon, India
About the role:
Accountable and responsible for creating and leading an appropriate Quality oversight organization and for designing, establishing and continuously improving a Quality Management System which ensures consistency in achieving process and product quality and compliance across multiple local Contract Organizations (CMOs, Contract Testing Organization, Distribution Organization) for clinical trial and commercial material. Responsible for critical quality and compliance decisions regarding locally manufactured, tested vaccine products for local and global distribution. In close collaboration with internal teams such as Vaccine Operations, Regulatory Affairs, and Legal team. This role negotiates contracts, and establishes policies with external contract organizations. Planning and managing functional budget including budget for work packages/activities at contract organization.
How you will contribute
- Provides strategic leadership and has accountability for external manufacturing & testing quality oversight of vaccines in the Asia region. Provides guidance on quality considerations and supports negotiation of contract terms across multiple sources of supply. Establishes & maintains contracts/policies/procedures. Responsible for making critical quality and compliance decisions regarding vaccine process & products manufactured/tested at Asia CMOs, including clinical trial material, commercial material, and starting (cell banks and virus banks) material.
- Drives collaboration with external partners in Asia to assure consistency in achieving process / product quality and compliance across multiple Contract Manufacturing Organizations (CMOs).
- Ensures product supply, compliance with local regulatory requirements, and global vaccines dossier in partnership with local cross functional internal partners for external supply, Regulatory Affairs, project management, process development and VBU Quality and Global Quality and regulators.
- Builds and leads the local QA team. Creates, develops, deploys and maintains an adequate and effective QMS system. Ensures timely execution of Quality Assurance and Quality Operations tasks and appropriate cGMP oversight to ensure successful tech transfer and subsequent commercial supply continuation. Shapes the long-term strategy and framework for vaccines External Supplier Quality in the region; including day to day operations such as review & approval of batch records, investigations, documents, change control, submission of batch specific documents to local authorities, batch disposition, process and analytical method performance monitoring and trending.
- Establishes, maintains, and monitors supplier files including Quality Agreements with CMOs and their suppliers.
- Plans, creates, and controls the department budget and budget related to CMO quality work-packages, aligns financial planning with strategic global VBU quality objectives & budget plan with Vaccines Operations partners.
- Act as the key-quality lead for CMO´s Site Quality Head and Senior Quality management team regarding vaccine operations executed at local CMOs and as the key quality partner for internal VBU and Takeda functions regarding vaccine manufacturing, testing, and supply in Asia, for Pan American Health Organization countries and for World Health Organization.
- Ensure cGMP requirements, Takeda expectations, and global dossier compliance are fulfilled for activities at contract facilities.
- Evaluates, defines and utilizes digital and automation tools to continuously drive operational excellence in collaboration with global functions.
- Establishes, maintains, and continuously improves system & processes to manage CMO change controls and investigations for issues associated with audits, manufacturing/testing events, and complaints, ensuring appropriate actions are implemented and aligned with VBU global product life cycle management and the company's strategic objectives.
- Establishes system & processes for manufacturing process and analytical method transfers from Takeda internal sites (or Takeda external partners) to local CMO. Provides quality guidance and oversight for specific tech transfers and ensures execution according to plans and protocols.
- Designs an appropriate oversight organization model that includes planning of resources to ensure regular representation of QA staff at CMO plant (Person In Plant), packaging site, laboratory, and warehouse/distribution center and leveraging insights to drive performance, strategic decision-making, quality risk management and continuous improvement.
- Organizes and participates in internal audits. Serves as an expert and key person for regulatory submissions.
- Enable vaccines national batch release through strong collaboration with local regulator and national control laboratories.
- Establishes and cascades functional goals based on GQ, VQ and VBU strategy and goals and development plans for the team, focusing on continuous improvement and Takeda’s Leadership Behaviors.
- Develops & establishes appropriate operating mechanisms with CMOs and with internal interface functions such as joint QCouncils, QRisk Registers, and KPI reviews to manage CMO performance and risk, aligning with the company's strategic objectives and long-term vision.
This position interacts frequently with:
- VBU Quality and VO leaders
- VBU QA team
- GMS QA and QC
- LOC QA
- RA-CMC (VBU)
- Local RA
- VBU Manufacturing Science Quality
- Global Pathogen Safety Team
- Corporate alliance partners and Takeda distribution partners
- Contract Manufacturing Organizations and Contract Testing Facilities
- Supply management
- Product Development, CMC Team Leaders
- National Control Laboratory and country MoHs
What you bring to Takeda:
Education and Experience Requirements
- Bachelor’s Degree or higher in Chemistry, Microbiology, or Life Sciences, or equivalent scientific discipline.
- Minimum of 7 years’ experience in quality assurance within the pharmaceuticals, biologics, vaccines experience preferred
- Management experience
- Good Manufacturing Practice experience, or experience in other regulated industry.
- Excellent communication skills both oral and written.
- Experience with supporting product inspections from global Regulatory Authorities such as WHO is required.
- Experience in tender business and requirements
- Experience in support of Tech Transfers and subsequent licensure for commercialization is required
- Effectively represent Quality Assurance, both internally and externally.
- Experience in routine Microsoft Office software packages and specialized software applications as appropriate.
- Exhibit and promote Takeda Core Competencies
Key Skills and Competencies
Equip with good knowledge of quality systems.
Equip with good knowledge in the various regulatory requirements.
Equip with good presentation skills.
Able to solve problems in a logical manner with timely solutions.
Able to interact and communicate with all types of personalities in an effective and diplomatic manner.
Project management skills is preferred.
Product release knowledge is preferred.
Be a delegate for QA line manager in his/her absence and approve any QA related documents.
Travel 30%
Locations
IND - GurgaonWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeSuccess profile
What makes a successful team member within Vaccines at Takeda?
- Integrity
- Fairness
- Inventive
- Perseverance
- Honesty
- Collaborative
Our leadership
Vaccines represent a new dimension of global impact — successful leadership at Takeda can be encompassed in these four pillars:
Demonstrating strategic enterprise thinking, finding innovative ways to serve patients and build trust, reputation and business
Creating the environment that inspires and enables people to move the organization forward
Focusing on the few priorities and delivers superior results
Elevating the capabilities of the organization for now and the future
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.
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.
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