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Jefferson Wells
Jefferson Wells

Quality Manager GMP

Published on Jobat.be 15 days ago

Quality Manager GMP

Quality Manager GMP

Hainaut – CDI

#quality #management #QA #assurance #continousimprovement #lean #GMP

Are you interested in the pharmaceutical industry and putting your knowledge of quality and people management to good use?

Our client is actively looking for a Quality Manager to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As Quality Manager, you are in charge to

  • Manage the Finished goods, QP and raw material team by defining in alignement with site QA objectives, the individual and team objectives, perform mid and end year review. Organize, manage and coach the different areas in a way that performance and objectives are achieved
  • Responsible for release of the final products in accordance with the applicable specifications and regulatory requirements for worldwide distribution
  • Responsible for the release the raw materials in accordance with the Raw Material Specifications, initiate the necessary actions in case of deviations
  • Deploy digitalization within the department, in line with the Digital strategy of the site.  Coach digital concepts, mindsets and behaviors to the team.
  • Empower individual in their personal development plan, identify the appropriate training to achieve personal objectives
  • Ensure and support continuous development and training of team members to achieve their daily activities and duties
  • Develop and stimulate employees to participate to the Continuous Improvement Programs (Lean, DMAIC, 5S, …)
  • Help to solve issues that the team is facing out and find way of improvement.
  • Participate to quality council and inspections
  • Develop and ensure that the procedures linked to the different activities are in line with the current regulations and guidelines.
  • Accountable for the adequate utilization of all quality systems as defined by procedures within his organization. Ensure a thorough and timely handling of associated tasks and activities.
  • Accountable/responsible for the Compliance to cGMP’s, GDP’s, Licenses and Procedures within his organization by defining, implementing and maintaining appropriate SOP’s and training.

Who are you?

  • 10 year experience in pharmaceutical sector (preferably in Quality)
  • QP (qualified person) is a plus
  • Excellent Team Management skills 
  • Focusing on priorities, handle multiple topics simultaneously in a high-volume environment, while meeting deadlines and attention to details
  • Demonstrated teamwork, initiative, and problem-solving skills
  • Stress-resistant, autonomous, Fact-based, critical thinking
  • Ability to work effectively with all levels of management and resolve problems in a timely manner
  • Excellent IT and digital system knowledge/capability
  • Good communication skills engaging stakeholders: team, site, business, network, company, regulators
  • French and English (written and spoken – advanced level) – mandatory

What can you expect?

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.

You’re interested in this job? We kindly invite you to apply directly on our website www.jeffersonwells.be. Do you have questions? You can contact diane.louppe@jeffersonwells.be or 0478/90.63.68.

Job description

Quality Manager GMP

Hainaut – CDI

#quality #management #QA #assurance #continousimprovement #lean #GMP

Are you interested in the pharmaceutical industry and putting your knowledge of quality and people management to good use?

Our client is actively looking for a Quality Manager to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As Quality Manager, you are in charge to

  • Manage the Finished goods, QP and raw material team by defining in alignement with site QA objectives, the individual and team objectives, perform mid and end year review. Organize, manage and coach the different areas in a way that performance and objectives are achieved
  • Responsible for release of the final products in accordance with the applicable specifications and regulatory requirements for worldwide distribution
  • Responsible for the release the raw materials in accordance with the Raw Material Specifications, initiate the necessary actions in case of deviations
  • Deploy digitalization within the department, in line with the Digital strategy of the site.  Coach digital concepts, mindsets and behaviors to the team.
  • Empower individual in their personal development plan, identify the appropriate training to achieve personal objectives
  • Ensure and support continuous development and training of team members to achieve their daily activities and duties
  • Develop and stimulate employees to participate to the Continuous Improvement Programs (Lean, DMAIC, 5S, …)
  • Help to solve issues that the team is facing out and find way of improvement.
  • Participate to quality council and inspections
  • Develop and ensure that the procedures linked to the different activities are in line with the current regulations and guidelines.
  • Accountable for the adequate utilization of all quality systems as defined by procedures within his organization. Ensure a thorough and timely handling of associated tasks and activities.
  • Accountable/responsible for the Compliance to cGMP’s, GDP’s, Licenses and Procedures within his organization by defining, implementing and maintaining appropriate SOP’s and training.

Who are you?

  • 10 year experience in pharmaceutical sector (preferably in Quality)
  • QP (qualified person) is a plus
  • Excellent Team Management skills 
  • Focusing on priorities, handle multiple topics simultaneously in a high-volume environment, while meeting deadlines and attention to details
  • Demonstrated teamwork, initiative, and problem-solving skills
  • Stress-resistant, autonomous, Fact-based, critical thinking
  • Ability to work effectively with all levels of management and resolve problems in a timely manner
  • Excellent IT and digital system knowledge/capability
  • Good communication skills engaging stakeholders: team, site, business, network, company, regulators
  • French and English (written and spoken – advanced level) – mandatory

What can you expect?

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.

You’re interested in this job? We kindly invite you to apply directly on our website www.jeffersonwells.be. Do you have questions? You can contact diane.louppe@jeffersonwells.be or 0478/90.63.68.

Profile

Quality Manager GMP

Hainaut – CDI

#quality #management #QA #assurance #continousimprovement #lean #GMP

Are you interested in the pharmaceutical industry and putting your knowledge of quality and people management to good use?

Our client is actively looking for a Quality Manager to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As Quality Manager, you are in charge to

  • Manage the Finished goods, QP and raw material team by defining in alignement with site QA objectives, the individual and team objectives, perform mid and end year review. Organize, manage and coach the different areas in a way that performance and objectives are achieved
  • Responsible for release of the final products in accordance with the applicable specifications and regulatory requirements for worldwide distribution
  • Responsible for the release the raw materials in accordance with the Raw Material Specifications, initiate the necessary actions in case of deviations
  • Deploy digitalization within the department, in line with the Digital strategy of the site.  Coach digital concepts, mindsets and behaviors to the team.
  • Empower individual in their personal development plan, identify the appropriate training to achieve personal objectives
  • Ensure and support continuous development and training of team members to achieve their daily activities and duties
  • Develop and stimulate employees to participate to the Continuous Improvement Programs (Lean, DMAIC, 5S, …)
  • Help to solve issues that the team is facing out and find way of improvement.
  • Participate to quality council and inspections
  • Develop and ensure that the procedures linked to the different activities are in line with the current regulations and guidelines.
  • Accountable for the adequate utilization of all quality systems as defined by procedures within his organization. Ensure a thorough and timely handling of associated tasks and activities.
  • Accountable/responsible for the Compliance to cGMP’s, GDP’s, Licenses and Procedures within his organization by defining, implementing and maintaining appropriate SOP’s and training.

Who are you?

  • 10 year experience in pharmaceutical sector (preferably in Quality)
  • QP (qualified person) is a plus
  • Excellent Team Management skills 
  • Focusing on priorities, handle multiple topics simultaneously in a high-volume environment, while meeting deadlines and attention to details
  • Demonstrated teamwork, initiative, and problem-solving skills
  • Stress-resistant, autonomous, Fact-based, critical thinking
  • Ability to work effectively with all levels of management and resolve problems in a timely manner
  • Excellent IT and digital system knowledge/capability
  • Good communication skills engaging stakeholders: team, site, business, network, company, regulators
  • French and English (written and spoken – advanced level) – mandatory

What can you expect?

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.

You’re interested in this job? We kindly invite you to apply directly on our website www.jeffersonwells.be. Do you have questions? You can contact diane.louppe@jeffersonwells.be or 0478/90.63.68.

Offer

Quality Manager GMP

Hainaut – CDI

#quality #management #QA #assurance #continousimprovement #lean #GMP

Are you interested in the pharmaceutical industry and putting your knowledge of quality and people management to good use?

Our client is actively looking for a Quality Manager to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As Quality Manager, you are in charge to

  • Manage the Finished goods, QP and raw material team by defining in alignement with site QA objectives, the individual and team objectives, perform mid and end year review. Organize, manage and coach the different areas in a way that performance and objectives are achieved
  • Responsible for release of the final products in accordance with the applicable specifications and regulatory requirements for worldwide distribution
  • Responsible for the release the raw materials in accordance with the Raw Material Specifications, initiate the necessary actions in case of deviations
  • Deploy digitalization within the department, in line with the Digital strategy of the site.  Coach digital concepts, mindsets and behaviors to the team.
  • Empower individual in their personal development plan, identify the appropriate training to achieve personal objectives
  • Ensure and support continuous development and training of team members to achieve their daily activities and duties
  • Develop and stimulate employees to participate to the Continuous Improvement Programs (Lean, DMAIC, 5S, …)
  • Help to solve issues that the team is facing out and find way of improvement.
  • Participate to quality council and inspections
  • Develop and ensure that the procedures linked to the different activities are in line with the current regulations and guidelines.
  • Accountable for the adequate utilization of all quality systems as defined by procedures within his organization. Ensure a thorough and timely handling of associated tasks and activities.
  • Accountable/responsible for the Compliance to cGMP’s, GDP’s, Licenses and Procedures within his organization by defining, implementing and maintaining appropriate SOP’s and training.

Who are you?

  • 10 year experience in pharmaceutical sector (preferably in Quality)
  • QP (qualified person) is a plus
  • Excellent Team Management skills 
  • Focusing on priorities, handle multiple topics simultaneously in a high-volume environment, while meeting deadlines and attention to details
  • Demonstrated teamwork, initiative, and problem-solving skills
  • Stress-resistant, autonomous, Fact-based, critical thinking
  • Ability to work effectively with all levels of management and resolve problems in a timely manner
  • Excellent IT and digital system knowledge/capability
  • Good communication skills engaging stakeholders: team, site, business, network, company, regulators
  • French and English (written and spoken – advanced level) – mandatory

What can you expect?

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.

You’re interested in this job? We kindly invite you to apply directly on our website www.jeffersonwells.be. Do you have questions? You can contact diane.louppe@jeffersonwells.be or 0478/90.63.68.

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    13 days left to apply

    Characteristics

    Requirements

    • Master (University or Higher Education Long Type)
    • French

    Offer

    • Permanent
    • Full-time

    Apply before

    • 30 April

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