Quality Manager (Kazakhstan, Kyrgyzstan, Mongolia)
Almaty Kazakstan
16 часов назад

Data de publication :

Oct 11 2019

Are you energized by a quality assurance role that allows you to accelerate compliance in a state of the art manufacturing environment?

If so, this Operational QA Manager role could be an ideal opportunity to explore.

As an Operational QA Manager, you will be responsible for providing effective and efficient support to the Local Operating Country (LOC) Quality Manager to maintain effective Quality Management System (QMS) and perform LOC Quality Operation activities in compliance with GSK Policies, QMS and local regulations.

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following :

  • Execute and deliver Local Operating Country (LOC) Quality Objectives and LOC Quality Improvement Plan.
  • Perform trending of Quality KPIs to support continuous improvement at the LOC.
  • Maintain a robust, sustainable and effective QMS (Quality Management System) at the LOC to ensure LOC Quality operations and processes are in full compliance with GSK standards and policies, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and local regulatory requirements.
  • Responsible for quality performance of the assigned 3rd party contractors / service providers / suppliers and ensuring potential quality and compliance issues are identified, communicated and promptly resolved.
  • Ensure quality systems are in place and in use according to GSK QMS standard.
  • Coordinate LOC Quality Council meetings.
  • Participate in LOC Quality Council(s) in identifying Quality related issues and continuous improvement Opportunities.
  • Perform activities to support risk management process to ensure timely mitigation of quality risks.
  • Perform quality impact assessment to ensure all planned changes at the LOC are appropriately managed.
  • are appropriately managed through change control.

  • Perform self-inspections at the LOC and 3rd party service providers’ operations with potential product quality and regulatory compliance impact.
  • Support investigations and root cause analysis in response to deviations, quality issues, audit findings and customer complaints.
  • Ensure product supplied to market have the right quality, safety, efficacy and comply with local regulations.
  • Why you?

    Basic Qualifications :

    We are looking for professionals with these required skills to achieve our goals :

  • Associate degree
  • 5 years of experience in life sciences industry in Quality Assurance role
  • Experience with cGMP (Clinical Good Manufacturing Practices) in pharma testing / secondary repacking
  • Operational experience with Good Documentation Practices (GDP) in warehousing and distribution
  • Preferred Qualifications :

    If you have the following characteristics, it would be a plus :

  • Bachelor’s degree
  • Ability to engage and works well works well in cross-functional teams
  • Ability to multi-task and work under pressure
  • Why GSK?

    Our values and expectations are at the heart of everything we do and form an important part of our culture.

    These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.

    As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities :

  • Operating at pace and agile decision-making using evidence and applying judgement to balance pace, rigour and risk.
  • Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
  • Continuously looking for opportunities to learn, build skills and share learning.
  • Sustaining energy and well-being.
  • Building strong relationships and collaboration, honest and open conversations.
  • Budgeting and cost-consciousness.
  • This is a job description to aide in the job posting, but does not include all job evaluation details.
  • Coordonnées :

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    L'obtention d'une autorisation écrite préalable est une condition préalable à tout accord (oral ou écrit) entre la société de recrutement / l'agence pour l'emploi et GSK.

    En l'absence d'une autorisation écrite, toute action de la part de la société de recrutement / l'agence pour l'emploi sera jugée comme ayant été effectuée sans le consentement ou l'accord contractuel de GSK.

    GSK ne pourra par conséquent pas être tenue responsable des frais découlant de ces actions ou des frais découlant de recommandations par des sociétés de recrutement / agences pour l'emploi en ce qui concerne les postes à pourvoir sur ce site.

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