supply chain market operations Quality ManagerPfizer Asia Pacific Pte Ltd

Job Description
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of Pfizer's dedicated and highly effective quality assurance and control team. You will be responsible for activities involved in developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines. Your contribution in quality risk management will help us in commitments tracking, interpreting policies, manage site complaints and work directly with operating entities to provide process analyses oversight. Thanks to you, we will be prepared for all upcoming audits and inspections. You will be relied on to ensure that the quality assurance programs and policies are maintained and modified regularly. You will make sure that there are uniform standards worldwide and best practice sharing, which will help in fostering the achievement of company's mission globally.
As a Manager, your breadth of knowledge on internal or external business challenges will help us improve our products, processes and services. Your will guide us to lead projects by meeting objectives and preparing forecasts for resource requirements. Your risk-taking ability will help us advance new concepts and methodologies. You will provide technical guidance and oversight to team members and help in problem solving.
It is your managerial skills and hard work that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Manage multiple projects and ongoing work activities in the department typically involving cross-functional representatives.
Support with resource planning activities measuring team productivity and identifying issues or opportunities.
Ensure processes associated with sustaining an inspection readiness state are maintained.
Provides guidance to SCMOQ team and areas personnel in resolving Quality events.
Communicate to the network key learnings at any of our sites through a regulatory audit or emerging regulations.
Recommend procedures and specification modifications to Divisional Quality Operations, whenever necessary.
Remain up-to-date on current Regulatory trends as well as Pfizer Quality Standards.
Work with Pfizer Global Supply groups and provide monthly training completion report to update the training records in the Learning Solution System.
Maintain vendor service contracts and requalification requirement for all Good Manufacturing Practices also cGMP related laboratory equipment and instrumentation.
Manage SCMOQ operations and Compliance functions and their associated records consistent with divisional/Corporate Regulatory Policy and Procedures.
Support the Site Quality Leader in the preparation of the annual budget based on the best information available.
Demonstrate a flexibility and agility to fit any future business needs.
Qualifications
Must-Have
Bachelor's Degree
A minimum of 7 years in the pharmaceutical industry, preferably in a quality role
A minimum of 5 years leading a team of colleagues
Demonstrated ability to influence, when necessary, particularly with stakeholders and external parties
A track record of continuous improvement and balancing efficiencies and effectiveness in processes
Ability to communicate across all levels of the organisation and also use communication to demonstrate the value of the quality organisation
Experience in auditing with Good Manufacturing Practices also cGMP regulated industries required.
Successful track record of continuous improvement and development / implementation of best practices in Quality market operations or manufacturing
Knowledge of national and international regulations relevant to the production and control of pharmaceutical products
Highly motivated, organized and able to work effectively in a demanding environment with flexibility to changing priorities
Strong people management experience
Fluent in English, both speaking & writing
Knowledge of electronic systems including Laboratory Information Management System Application and Products, MS Word and MS Excel
Nice-to-Have
Master's degree
Relevant pharmaceutical experience
Experience in aseptic manufacturing
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Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
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