Loc Quality Executive Gne - Bengaluru, India - Haleon

Haleon

Verified Company

Bengaluru, India

2 weeks ago

Posted by:

Deepika Kaur

beBee Recuiter

Description

LOC Quality Executive GNE:

Dubai, United Arab Emirates
Quality

gsknch

Job Description:

Site Name:
UAE - Dubai

-
Posted Date: Oct

Hello. We're Haleon. A new worldleading consumer healthcare company. Shaped by all of us. Together, we're improving everyday health for millions of people. By growing and innovating our global portfolio of categoryleading brands including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're building together. In an environment that we're cocreating. And a culture that's uniquely ours. Care to join us. It isn't a question.

Job Purpose:

The LOC Quality Executive roles exists to provide effective and efficient quality assurance systems support to the LOC Quality Manager, including supporting the implementation and maintenance of the QMS and as directed by the LOC Quality Manager performs the day-to-day work to ensure that the quality systems required by the LOC element of the Supply Chain and Marketing Company LOC are performed in a lean and efficient way and meet the compliance standards of the QMS and the local Regulator.

The LOC Quality Executive will act as Quality Representative within the Commercial Team supporting the delivery of quality management system for the nominated country.

The role holder will also partner with the business to ensure that their business requirements are understood.

The role will drive a quality culture within the LOCs.

The role will drive standardized business processes where applicable across LOC to maximize business benefits

Key Responsibilities:

Maintain a high level of QMS knowledge and awareness of changes within the commercial environment to seek opportunities and manage potential business adversity. Supporting the LOC Quality Manager to ensure a robust, sustainable and effective QMS (Quality Management System) through monitoring and reviewing the compliance status within the LOC element of the end to end Quality.
Ensure that all SOPs are in place, updated & training has been conducted across the business. Ensure a monitoring system in place for tracking training compliance and process for escalation of persistent noncompliance.
Promote QMS management principles and seek continuous improvement of the processes
LOC Quality Council support the LOC Quality Manager re organizing Council meeting with regular meetings.
Change Control perform day to day work to support the local change control process with the aim of ensuring all planned major changes
Risk Management perform activities to support the risk management process to ensure effective management, timely reporting, review and escalation of quality risks.

Artwork management

Support day to day work in line with the roles and responsibilities for quality as defined in the local artwork procedures.
Local Repacking perform day to day work to support repacking requests ensuring regulatory and QA compliance, timely QA batch release of repacked orders before distribution and/or reexport. Ensure as appropriate documentation of batch records and retention of samples.
Quality

Regulatory Intelligence - impact assessment & business evaluation for all QRI's impacting LOC

Quality

Alerts/Quality Bulletins - support in the evaluation and implementation of the action plans of applicable received alerts/bulletins.

Auditing perform day to day work to support the local process that is in place for selfinspection (MM) and independent business monitoring (IBM). Work with the LOC Quality Manager to ensure
Complaints perform day to day work to support an effective complaints management process

Incident management

Support the LOC Quality Manager to ensure that an effective local product incident process is in place to escalate and manage any product quality related issues
Third Party Management performs day to day work to support systems that have an impact on the quality of imported, products in line with the QMS and local Regulatory requirements
Documentation and Data Management
Maintains all quality documentation such as product specifications and Standard Operating Procedures in accordance with the QMS policies.
Quality

Governance Reporting

Ensure timely reporting for all QMS topics that are reported into the Global KPI reporting process
Ensure correct and timely reporting to area KPI reporting process

Why you?

Basic Qualifications

Education & Experience:

This role requires a deep level of GMP/GDP knowledge and problemsolving skills due to the often complex and technical origin of product quality issues and events
At least 5 years of relevant working experience in the pharmaceutical/consumer healthcare/medical device industries in Quality Assurance role
The holder is required to interact with 3rd party contract