Senior Director, Quality Assurance
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Our mission is clear: We want people with a hearing loss to be able to experience high life quality. We want to develop the world’s best hearing healthcare solutions. Nothing less… and to do so, we need you!
As the Senior Director of Quality Assurance, you will be responsible for our quality assurance efforts to ensure that our hearing aids consistently meet the highest standards of quality and performance. You will have an important role in maintaining compliance with relevant regulatory requirements, establishing robust quality management systems, and ensuring a culture of continuous improvement throughout the organization.
Sounds like you? Then read on!
Welcome to Quality in HIG
Quality Assurance is a part of the Quality function and is placed in the Hearing Instrument Group (HIG). The Quality function consists of 200+ colleagues globally, and we are responsible for Quality and Regulatory for our biggest brands, like Oticon, Bernafon and Philips.
You will head up the Quality Assurance team, where seven highly engaged specialists and three senior project managers work together every day to ensure that our products meet and exceed the highest quality standards, regulatory requirements, and customer expectations.
The main activities of the Quality Assurance team are documentation control, CAPA Process, QMS update and maintenance, calibration process, and planning and execution of internal/external audits in Demant relevant sites. The team is located both in Denmark and Poland.
You will also head up the Quality Strategy projects which are developed with respect to the overall strategy and are cross functional. Your role will be to coordinate, support and engage the Quality project leaders, and manage and monitor the Quality project portfolio.
In the Quality function you will, besides Quality Assurance, find Product Quality, Regulatory Affairs, Global Operations Quality and Product Support. You will work closely with your fellow Senior Directors in coordinating day to day activities and plan long-term strategic initiatives.
Support and develop your team and work on strategic business initiatives
This position offers a unique opportunity to contribute to the development and delivery of cutting-edge hearing aid technologies that improve the lives of millions of people worldwide.
Your role is to manage, support and develop the Quality Assurance team in the best and most strategic way going forward. Here you will lead and coach your direct reports, facilitate improvement activities and provide mentorship, guidance, and performance evaluations.
You will also
As a part of the Quality Leadership Team, your insights, input to the strategy and teamwork will be an important contribution.
“You will become a part of a great Quality leadership team where opinions count and we really value each other’s input, no issue is too small or too big”. says your new manager, Senior Vice President, Quality, Veronique Schou
Your role will interface within Quality as well as outside across the global organization. Your main key stakeholders are the Quality function, Hearing Instrument Management Group, and the management in R&D, Sales & Marketing, IT, HR and Operations.
“Collaboration is key here! It’s vital that there is a well-functioning collaboration with cross-functional teams to integrate quality processes throughout the product lifecycle.” says Veronique
You should expect travelling days to be around 10-30 days, primarily to your team in Poland, but other travels linked to audit can also occur.
Experienced people manager with Quality Assurance background
You probably have a technical or commercial/business degree, but your experience is more important to us. Ideally you have minimum 3 years’ experience as QA manager from a large international company.
As a Medical Device manufacturer, we are looking for solid compliance and regulation knowledge within ISO13485, Medical Device Regulation (MDR), FDA CFR 21 part 820 and MDSAP.
You have proven leadership and team management skills, with the ability to motivate and inspire a diverse team of professionals. You have good competences within coaching, delegating and transformational leadership.
Your personal mark
To thrive in this position, you articulate clearly and naturally your point and directions. You have an open communication style and approachable attitude among your peers and stakeholders.
You have eyes on target, follow through and carry out: you can put initiatives into action, uncover risks, and you have the ability to solve them by mitigation.
Moreover, we work in a matrix organization which means you need to be a good relationship builder.
We dare to make a difference
We are at the forefront of the latest technology. You will be seizing an opportunity to be part of a growing international company with a collaborative environment built on trust and openness, and a strong motivation.
Please send your CV and application as soon as possible. The application deadline is 20th August 2023. Please note, we only accept applications through our online application system.
If you are curious to know more about the job, you are welcome to contact Veronique Schou, Senior Vice President, Quality at [email protected]
We look forward to meeting you.
As the Senior Director of Quality Assurance, you will be responsible for our quality assurance efforts to ensure that our hearing aids consistently meet the highest standards of quality and performance. You will have an important role in maintaining compliance with relevant regulatory requirements, establishing robust quality management systems, and ensuring a culture of continuous improvement throughout the organization.
Sounds like you? Then read on!
Welcome to Quality in HIG
Quality Assurance is a part of the Quality function and is placed in the Hearing Instrument Group (HIG). The Quality function consists of 200+ colleagues globally, and we are responsible for Quality and Regulatory for our biggest brands, like Oticon, Bernafon and Philips.
You will head up the Quality Assurance team, where seven highly engaged specialists and three senior project managers work together every day to ensure that our products meet and exceed the highest quality standards, regulatory requirements, and customer expectations.
The main activities of the Quality Assurance team are documentation control, CAPA Process, QMS update and maintenance, calibration process, and planning and execution of internal/external audits in Demant relevant sites. The team is located both in Denmark and Poland.
You will also head up the Quality Strategy projects which are developed with respect to the overall strategy and are cross functional. Your role will be to coordinate, support and engage the Quality project leaders, and manage and monitor the Quality project portfolio.
In the Quality function you will, besides Quality Assurance, find Product Quality, Regulatory Affairs, Global Operations Quality and Product Support. You will work closely with your fellow Senior Directors in coordinating day to day activities and plan long-term strategic initiatives.
Support and develop your team and work on strategic business initiatives
This position offers a unique opportunity to contribute to the development and delivery of cutting-edge hearing aid technologies that improve the lives of millions of people worldwide.
Your role is to manage, support and develop the Quality Assurance team in the best and most strategic way going forward. Here you will lead and coach your direct reports, facilitate improvement activities and provide mentorship, guidance, and performance evaluations.
You will also
- promote the QA strategic initiatives
- manage and administer our Quality Management System according to applicable regulations and standards
- develop and prioritize an audit strategy for all sites and all manufacturing locations. Contact person to Notified Body
- support wholesales and guide the organization through quality assurance knowledge
As a part of the Quality Leadership Team, your insights, input to the strategy and teamwork will be an important contribution.
“You will become a part of a great Quality leadership team where opinions count and we really value each other’s input, no issue is too small or too big”. says your new manager, Senior Vice President, Quality, Veronique Schou
Your role will interface within Quality as well as outside across the global organization. Your main key stakeholders are the Quality function, Hearing Instrument Management Group, and the management in R&D, Sales & Marketing, IT, HR and Operations.
“Collaboration is key here! It’s vital that there is a well-functioning collaboration with cross-functional teams to integrate quality processes throughout the product lifecycle.” says Veronique
You should expect travelling days to be around 10-30 days, primarily to your team in Poland, but other travels linked to audit can also occur.
Experienced people manager with Quality Assurance background
You probably have a technical or commercial/business degree, but your experience is more important to us. Ideally you have minimum 3 years’ experience as QA manager from a large international company.
As a Medical Device manufacturer, we are looking for solid compliance and regulation knowledge within ISO13485, Medical Device Regulation (MDR), FDA CFR 21 part 820 and MDSAP.
You have proven leadership and team management skills, with the ability to motivate and inspire a diverse team of professionals. You have good competences within coaching, delegating and transformational leadership.
Your personal mark
To thrive in this position, you articulate clearly and naturally your point and directions. You have an open communication style and approachable attitude among your peers and stakeholders.
You have eyes on target, follow through and carry out: you can put initiatives into action, uncover risks, and you have the ability to solve them by mitigation.
Moreover, we work in a matrix organization which means you need to be a good relationship builder.
We dare to make a difference
We are at the forefront of the latest technology. You will be seizing an opportunity to be part of a growing international company with a collaborative environment built on trust and openness, and a strong motivation.
Please send your CV and application as soon as possible. The application deadline is 20th August 2023. Please note, we only accept applications through our online application system.
If you are curious to know more about the job, you are welcome to contact Veronique Schou, Senior Vice President, Quality at [email protected]
We look forward to meeting you.
Information og data
Denne ledige stilling har jobtypen "Direktør", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Smørum.
Jobbet er oprettet på vores service den 14.8.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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