LOC Quality Executive
- Bachelor Degree or Diploma in scientific discipline, or able to demonstrate equivalent level of knowledge
- Minimum of 3 years in Quality experience within the Pharma industry and application of Quality Systems
- Strong interpersonal and negotiation skills
- Problem identification and solving skills
- Self-starter, able to schedule and progress workload on own
- Knowledge of regulatory requirements pertaining to GMP/GDP
- Knowledge on effective quality documentation systems
- Professional written and verbal communication skills.
- Ability to deliver clear communications and foster excellent working relationships with peers and management
- Analytical mind, good attention to detail and problem solving skills within a structured process
- Good team player – works well in cross-functional teams
- Ability to multi-task and work under pressure
- Concise in the description of the different QA situations. Able to stick to the standard and not be pressurized.
- Works with a spirit of continuous improvement and innovation, creatively open to new ideas and methods
- Flexible thinking – able to challenge and see views from different perspectives
- Ability to self-motivate and be resilient and focused under pressure
- Strong general computer literacy with Intermediate skills in Microsoft Word, Excel, Power Point and Outlook.
The LOC Quality Executive roles exists to provide effective and efficient quality assurance systems support to the LOC Quality Hub Manager or 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 area or country. The role holder will also partner with the business to ensure that their business requirements are understood.
The role will take supporting role to drive a quality culture within the LOCs.
- 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 Supply Chain and Markets.
- Maintain a high level of QMS knowledge and awareness of changes within the commercial environment to seek opportunities and manage potential business adversity.
- Support the implementation and maintenance of effective Quality Assurance systems to ensure that local operations are in full compliance with GSK standards and policies, Guide for Commercial Companies ,GMP, GDP and regulatory requirements by supporting the LOC Quality Manager as directed
o 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 non-compliance. Processes in place for delivering routine training for updates to SOPs, GQPs, and GQMPs as relevant.
o Promote QMS management principles and seek continuous improvement of the processes
o Review, conduct impact assessments and implement any updates to QMS policies
o Manage QMS Management Review meetings according to local SOPs
o Identify, Implement and Manage QA Objectives & KPIs
o Establish and manage Annual Quality Plans
- Support the LOC Quality Manager to ensure that all internal procedures and systems in use in the LOC are compliant to GSK QMS, Guide for Commercial Companies and local regulatory requirements, including (but not limited to)
o LOC Quality Council – support the LOC Quality Manager re organizing Council meeting with regular meetings. This support should ensure that the LOC Quality Council format, frequency and reporting are standardised to global requirements. In addition support should be provided re Quality metrics and reporting format/ system in place.
o Change Control - perform day to day work to support the local change control process with the aim of ensuring all planned major changes (including as appropriate new pack introduction, product discontinuation, major pack changes, re-packing activities) are effectively and compliantly managed. Processes in place to routinely review progress of changes and close out when completed.
o Risk Management - perform activities to support the risk management process to ensure effective management, timely reporting, review and escalation of quality risks.
o Corrective and Preventative Actions (CAPA) - Implement global or local process to effectively manage corrective and preventative action plans. Develop local processes to conduct root cause analysis to investigate deviations and develop CAPA's. Local process in place to track and review CAPA plans on routine basis. Demonstrate that LOC effectively identifies where CAPA plans required and that they are effectively implemented, monitored and closed out.
o Auditing - perform day to day work to support the local process that is in place for Level 1 (self-inspection) and Level 2 monitoring auditing. Work with the LOC Quality Manager to ensure
Level 1 and Level 2 auditing process includes clear accountability for sign off of audit reports and resultant CAPA/ Risk management.
Level 1 and Level 2 audit universe is defined and agreed with Regional Quality and annual audit schedules in place.
There is a process in place to ensure all new and existing suppliers/ 3rd party contractors/ service providers that have a direct impact on product quality are identified and audited by either LOC QA Team or the appropriate Central Team (e.g. ESA). e.g. distribution sites, repacking contractors, warehouses, freight management, samples supply, off-site archive sites, artwork printers, printed packaging component suppliers.
Availability if requested to participate in Level 1 (self) and Level 2 audits with the agreement of the relevant Central Team
LOC element of the Supply Chain and the Quality elements of the Marketing Company are audit ready for any relevant Level 3 or 4 audits.
o Complaints - perform day to day work to support an effective complaints management process ensuring
the assessment of potential issues are determine as quickly as possible and linked to the adverse event reporting process and local product incident process if/as appropriate.
report and follow up on product complaints with manufacturing sites, customers and commercial teams.
o 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 and in the training of all relevant staff in local incident management process and global PIRC process. Assist the LOC Quality Manager in any investigations triggered by local incidents and in conducting LOC Incident Committees.
o Product supply - 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
responsible for the review and at the direction of the LOC Quality Manager the approval of TTS (Technical Terms of Supply) and liaison with manufacturing sites to ensure compliance to local registered technical details.
Liaison with External Supply Quality for products that are manufactured by contractors to ensure compliance to local registered technical details.
Ensure timely local Quality release of imported finished goods deliveries and resolve Quality-related issues arising from these deliveries. Support the LOC Quality Manager with communication to the GMS supplying sites, R&D and Regional Quality as it relates to approval of repacking activities and resolving Quality issues with the product supplied
o Artwork management - perform day to day work in line with the roles and responsibilities for quality as defined in the local artwork procedures.
o 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 re-export. Ensure as appropriate documentation of batch records and retention of samples.
- Maintains all quality documentation such as product specifications and Standard Operating Procedures in accordance with GSK policies.
o Ensures all product specifications and related documents (e.g. CoAs, TTs) are maintained compliant to current registered details.
o Maintains and updates the QA Standard Operating Procedures
You may apply for this position online by selecting the Apply now button.
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