Apply for Quality Specialist Role at Sanofi US

Malaysia Job Openings

Sanofi US

Quality Specialist

Petaling Jaya

FULL TIME

October 15, 2024

About the Job
You will be part of the Quality team to ensure Quality operations and processes provide maximum value to the Business Operations across assigned markets, whilst meeting applicable local national Gx P & regulatory requirements as well as Sanofi standards & business expectation and continuity. You will ensure an efficient, effective and proactive Quality Product, System and performance delivery and handle country quality operation input into plans for product commercialization & rationalization.

In this role, you will support the country quality operations for Malaysia, Brunei and Singapore and act as back- up to quality operations for Partner Markets countries, where you will co-ordinate and handle quality management processes and activities as per the quality agreement in these markets.

Main Responsibilities:
Product Quality and Related Quality Systems

Handle product quality and related Quality systems according to Sanofi processes, standards and appropriate tools in force, in connection with the concerned Global Quality functions.
Coordinate and handling product technical complaints received from the market according to Sanofi processes, standards, and appropriate tools in force, in connection with the concerned Global Quality functions.
Manage product- related quality events such as product recalls and escalate quality events as necessary according to defined processes and standards.
Coordinate in product recall management of EWD according to quality agreement in accordance with local regulation.
Coordinate and communicate on Quality matters to the appropriate functions at country level and EWD according to the defined responsibilities vis à vis Regulatory Authorities
Perform local batch release and, vaccines batch release certification from Health Authority (HA).
Monitor local GMP/ GDP activities (e.g., repackaging, storage, distribution, etc.) are performed in accordance with applicable GMP and GDP regulations.

Management of Country Quality System

Coordinate with Country Quality system for Gx P and health-regulated activities from development to commercialisation of all products and related Gx P services, in compliance with Sanofi quality documents and standards, as well as applicable local regulatory requirements.
Coordinate a network of professionals designated in each country function involved in Gx P and health-regulated activities and embark them to address all matters related to Quality, including the support to business and digital initiatives.
Maintain the Country Quality documentation management system, ensuring all process for management of Gx P documents and records is in place in all Gx P and health-regulated areas, considering data integrity principles.
Participate and co-ordinate Country Quality audits and Gx P regulatory inspections.
Evaluate trends in local quality audit findings that may affect the Country Quality system and communicate audit findings that require improvement to the appropriate global functions.
Remain up to date on Gx P system quality audit reports concerning the country, including any conclusions, decisions made, as well as actions plans.
Perform training sessions and maintain personal qualification to be qualified in role and responsibility.
Prepare and provide input to the country Quality Review and organize presentation to Country Senior Management.
Deviation and Corrective- Preventive Actions (CAPA) Management and change control management.
Prepare and maintain valid and signed quality agreements with appropriate Sanofi manufacturing and distribution sites or/ and external organizations.
Provide quality oversight of locally managed Gx P subcontractors.
Maintain administrative records such as training log, job description as per Gx P requirements
Maintenance of local inventory of Gx P Computerized Systems (CS), validated by relevant internal functions.
Enhance Quality culture & promote Quality mind-set into the country governance, working principles and ways of operating.
Act as back up to CQH for MYBR and Quality Management Ops MYBRSG, in critical quality matters; Quality Alerts, recall, regulatory matters and to ensure business continuity.

Quality Oversight of External Wholesale Distributor (EWD) in Partner Markets.

Prepare and maintain of Quality and Technical Agreements in the business contract with EWD.
Quality oversight and ensure process is in adherence to quality governance model.
Conduct the relevant reconciliations between Gx P functions and EWD.
Maintain Quality Agreements with the Manufacturing sites and/or foreign MAH entities, where required.

About You

Experience: Minimum 5 years of experience in Quality Assurance, Quality Management System in relevant industry.
Technical skills: Familiar with Gx P requirements, health regulations and Quality Management System.
Education: Bachelor's Degree in Pharmaceutical Sciences or similar disciplines.
Excellent written and oral communication skills.

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including health insurance, out-patient benefits along with a range of family friendly policies such as maternity, paternity, and solo parent leaves to name a few.

We regret to inform you that this job opportunity is no longer available as it has expired

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