Senior Project Manager - Building Management Systems

Innovate to solve the world's most important challenges

The Project Manager is responsible for management of medium to large jobs including leading the project technicians and sub-contractors, etc. This support will consist of forecasting, planning, risk identification, change order management, billing and payments. The PM takes full P&L responsibility for the complete project and report to the Country Project Management Lead.

Core duties

  • on time and on budget delivery of Contract Commitment, include subcontract quality management, progress tracking, application for cash management, site engineering, coordination and task management, and project planning for assigned activities;
  • manages assigned technical work force and customer satisfaction.

Primary responsibilities include

  • Ensures on time delivery of projects, within scope with zero or positive deviation.
  • Leads creation and maintenance of the project plan. Works with the customer’s project management to coordinate major milestones and resolve schedule issues.
  • Monitor the project processes, to identify opportunities for improving the project financial results, based on project changes and events (schedule, scope, hindrances etc.) and initiates/takes action to obtain these.

Your Profile

  • Electrical background – Engineering / Management degree is desired but not mandatory
  • 3-5 years’ demonstrated experience in delivering projects within the Building Solutions Business within construction industry
  • Deep understanding of project operations and financial processes
  • Fluent in Danish English
  • PMI Certification would be an asset
  • You love driving project forward and deliver beyond customer expectations. To be successful, you need have a boundless drive and is well-structured.

We offer 

You will have a competitive compensation package and be part of professional team. You will work with state of the art technology, where we install, integrate and maintain system that keep facilities safe, secure and energy-efficient.

Apply

Please send your application and CV as soon as possible. Recruitment is handled by Deichborg & More. Feel free to contact researcher, Michael Kock at tel. 4278 4278 or mko@deichborgmore.com.

About

Honeywell is a global leader in the areas of technology and advanced manufacturing processes. In more than 120 countries around the world, about 131,000 employees develop and manufacture reliable and state-of-the-art-products in the fields of Aerospace, Building Technologies, Performance Materials and Safety and Productivity Solutions.Honeywell Building technologies, deliver products, software, and technologies that are installed in more than 10 million buildings worldwide, helping customers ensure their facilities are safe, energy efficient, sustainable, and productive.In the BMS partner channel Nordic Honeywell educate highly professional partners which deliver and install our solutions in commercial buildings like offices, hotels, schools, hospitals, data centers and state of the art cruise ships.


Du har ikke vedlagt dokumenter til din ansøgning. Klik på 'OK' knappen nedenfor for at sende din ansøgning alligevel, eller klik på knappen "Annuller" og vedhæft dokumenter, før du sender din ansøgning igen.

Mere af samme slags?

Angiv din e-mail og få lignende job direkte i indbakken




Når du tilmelder dig accepterer du samtidig vores privativspolitik

330040326Phoenix-8eac43c812019-06-09T00:00:00Senior Project Manager - Building Management Systems

Innovate to solve the world's most important challenges

The Project Manager is responsible for management of medium to large jobs including leading the project technicians and sub-contractors, etc. This support will consist of forecasting, planning, risk identification, change order management, billing and payments. The PM takes full P&L responsibility for the complete project and report to the Country Project Management Lead.

Core duties

  • on time and on budget delivery of Contract Commitment, include subcontract quality management, progress tracking, application for cash management, site engineering, coordination and task management, and project planning for assigned activities;
  • manages assigned technical work force and customer satisfaction.

Primary responsibilities include

  • Ensures on time delivery of projects, within scope with zero or positive deviation.
  • Leads creation and maintenance of the project plan. Works with the customer’s project management to coordinate major milestones and resolve schedule issues.
  • Monitor the project processes, to identify opportunities for improving the project financial results, based on project changes and events (schedule, scope, hindrances etc.) and initiates/takes action to obtain these.

Your Profile

  • Electrical background – Engineering / Management degree is desired but not mandatory
  • 3-5 years’ demonstrated experience in delivering projects within the Building Solutions Business within construction industry
  • Deep understanding of project operations and financial processes
  • Fluent in Danish English
  • PMI Certification would be an asset
  • You love driving project forward and deliver beyond customer expectations. To be successful, you need have a boundless drive and is well-structured.

We offer 

You will have a competitive compensation package and be part of professional team. You will work with state of the art technology, where we install, integrate and maintain system that keep facilities safe, secure and energy-efficient.

Apply

Please send your application and CV as soon as possible. Recruitment is handled by Deichborg & More. Feel free to contact researcher, Michael Kock at tel. 4278 4278 or mko@deichborgmore.com.

About

Honeywell is a global leader in the areas of technology and advanced manufacturing processes. In more than 120 countries around the world, about 131,000 employees develop and manufacture reliable and state-of-the-art-products in the fields of Aerospace, Building Technologies, Performance Materials and Safety and Productivity Solutions.Honeywell Building technologies, deliver products, software, and technologies that are installed in more than 10 million buildings worldwide, helping customers ensure their facilities are safe, energy efficient, sustainable, and productive.In the BMS partner channel Nordic Honeywell educate highly professional partners which deliver and install our solutions in commercial buildings like offices, hotels, schools, hospitals, data centers and state of the art cruise ships.

Innovate to solve the world s most important challenges The Project Manager is responsible for management of medium to large jobs including leading the project technicians and sub-contractors, etc. This support will consist of forecasting, planning, risk identification, change order management, billing and payments. The PM takes full P L responsibility for the complete project and report to the Country Project Management Lead. Core duties: on time and on budget delivery of Contract Commitment, include subcontract quality management, progress tracking, application for cash management, site engineering, coordination and task management, and project planning for assigned activities manages assigned technical work force and customer satisfaction. Primary responsibilities include Ensures on time delivery of projects, within scope with zero or positive deviation. Leads creation and maintenance of the project plan. Works with the customer s project management to coordinate major milestones and resolve schedule issues. Monitor the project processes, to identify opportunities for improving the project financial results, based on project changes and events (schedule, scope, hindrances etc.) and initiates takes action to obtain these. Your Profile Electrical background Engineering Management degree is desired but not mandatory 3-5 years demonstrated experience in delivering projects within the Building Solutions Business within construction industry Deep understanding of project operations and financial processes Fluent in Danish English PMI Certification would be an asset You love driving project forward and deliver beyond customer expectations. To be successful, you need have a boundless drive and is well-structured. We offer You will have a competitive compensation package and be part of professional team. You will work with state of the art technology, where we install, integrate and maintain system that keep facilities safe, secure and energy-efficient. Apply Please send your application and CV as soon as possible. Recruitment is handled by Deichborg More. Feel free to contact researcher, Michael Kock at tel. 4278 4278 or mko@deichborgmore.com. About Honeywell is a global leader in the areas of technology and advanced manufacturing processes. In more than 120 countries around the world, about 131,000 employees develop and manufacture reliable and state-of-the-art-products in the fields of Aerospace, Building Technologies, Performance Materials and Safety and Productivity Solutions.Honeywell Building technologies, deliver products, software, and technologies that are installed in more than 10 million buildings worldwide, helping customers ensure their facilities are safe, energy efficient, sustainable, and productive.In the BMS partner channel Nordic Honeywell educate highly professional partners which deliver and install our solutions in commercial buildings like offices, hotels, schools, hospitals, data centers and state of the art cruise ships.11jobnet8eac43c8100000000000aDK_OFIR_02DKDanmark228DKK2019-08-04T00:00:000000https://ssl.onerecruit.com/Apply/41603fb2-43c8-4454-a2c7-08c5bf3ff2d9/0EuropaDanmarkSjælland & øerStorkøbenhavnVallensbæk3544388EasySearch ApS11Strandesplanaden 1102665Vallensbæk StrandDKDanmark0DKDanmarkDKDanmark8Fuldtid46Permanent775656JobNet5002469500246910009-06-20190https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=8eac43c8https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=8eac43c8https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=8eac43c8&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=8eac43c8&page=EmailApplyForm&component=SendApplicationButton1Dansk3Læse/ tale938119Project Manager0Øvrige362060470noreply@ofir.comDKDanmarkDKDanmark330058539Senior Clinical Project ManagerRobot Would you like to play a key role in the development of our growing portfolio together with a friendly, ambitious and professional team in Trial Management? You will join a very successful company, dedicated towards fulfilling the vision of becoming the world s preferred dermatology care partner. With our ambitious aspiration to help more than 100 million people by 2020, LEO Pharma is looking at new and innovative solutions - now also entering into development of biological treatments. LEO Pharma is set to offer the most diverse range of treatment solutions to meet the individual needs of people with skin diseases. The Trial Management department at LEO Pharma in Copenhagen is looking for Senior Clinical Project Managers who can ensure the conduct of high-quality clinical trials from our wide range of exciting development projects. Tasks and responsibilities: You will oversee all aspects of the start-up, conduct, close-out and reporting of clinical trials. You will provide input toward production, review and approval of clinical trial documents. You feel comfortable in leading trials and drive timelines and deliverables within the team. You have the ability to visit KOL sites to develop and maintain relationships if necessary and ensure trial team members are adequately trained on the responsibilities of the trial conduct. You collaborate closely with stakeholders within Denmark and other international colleagues and team members, perform oversight of vendors and participate in the continuous improvement of the department s procedures to secure best practices. You must possess the following qualifications: As a minimum you have a bachelor s degree in science or equivalent relevant education or related experience gained in clinical research with at least 3 years of direct clinical trial management or related trial experience. You have a strong knowledge of the drug development process and can demonstrate strong project management skills with a proactive nature. You are a team player who can work with other functional areas and foster successful team spirit. You like to take on responsibility, working in a structured manner, committed, flexible and have a positive attitude. You are able to travel internationally and possess excellent communication skills in English, verbally as well as in writing. Are you ready to join us? We offer a challenging job as Senior Clinical Project Manager, where you will get the opportunity to be a key contributor to the success of LEO s exciting portfolio. You will be working together with an international team of dedicated colleagues within Global Clinical Operations as well as with other functional areas from LEO R D. The Trial Management department is placed in LEO Pharma s headquarter in Ballerup near Copenhagen, Denmark. You will have the opportunity to attend relevant workshops congresses to further develop your skills as project manager. We offer a challenging job in a global environment and aim to offer a competitive package. Furthermore, you will get the opportunity to contribute and be part of a flexible, pleasant and busy working environment in a well-run and informal department. We look forward to welcoming you to our team!

Would you like to play a key role in the development of our growing portfolio together with a friendly, ambitious and professional team in Trial Management?

You will join a very successful company, dedicated towards fulfilling the vision of becoming the world’s preferred dermatology care partner. With our ambitious aspiration to help more than 100 million people by 2020, LEO Pharma is looking at new and innovative solutions - now also entering into development of biological treatments. LEO Pharma is set to offer the most diverse range of treatment solutions to meet the individual needs of people with skin diseases. 

The Trial Management department at LEO Pharma in Copenhagen is looking for Senior Clinical Project Managers who can ensure the conduct of high-quality clinical trials from our wide range of exciting development projects. 

Tasks and responsibilities: 

You will oversee all aspects of the start-up, conduct, close-out and reporting of clinical trials. You will provide input toward production, review and approval of clinical trial documents. You feel comfortable in leading trials and drive timelines and deliverables within the team. You have the ability to visit KOL sites to develop and maintain relationships if necessary and ensure trial team members are adequately trained on the responsibilities of the trial conduct. You collaborate closely with stakeholders within Denmark and other international colleagues and team members, perform oversight of vendors and participate in the continuous improvement of the department’s procedures to secure best practices. 

You must possess the following qualifications: 

As a minimum you have a bachelor’s degree in science or equivalent/relevant education or related experience gained in clinical research with at least 3 years of direct clinical trial management or related trial experience. You have a strong knowledge of the drug development process and can demonstrate strong project management skills with a proactive nature. You are a team player who can work with other functional areas and foster successful team spirit. You like to take on responsibility, working in a structured manner, committed, flexible and have a positive attitude. You are able to travel internationally and possess excellent communication skills in English, verbally as well as in writing.

Are you ready to join us? 

We offer a challenging job as Senior Clinical Project Manager, where you will get the opportunity to be a key contributor to the success of LEO’s exciting portfolio. You will be working together with an international team of dedicated colleagues within Global Clinical Operations as well as with other functional areas from LEO R&D. The Trial Management department is placed in LEO Pharma’s headquarter in Ballerup near Copenhagen, Denmark. You will have the opportunity to attend relevant workshops/congresses to further develop your skills as project manager. We offer a challenging job in a global environment and aim to offer a competitive package. Furthermore, you will get the opportunity to contribute and be part of a flexible, pleasant and busy working environment in a well-run and informal department. 

We look forward to welcoming you to our team!

LEO PHARMA A/SBallerup2019-07-11T00:00:002019-08-15T00:00:00
330058540Project Manager with Quality experienceRobot This is your chance to join one of the world s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. Global Quality Projects is responsible for project management within Global Quality CI in LEO Pharma and we are looking for an experienced Project Manager to drive global quality projects in a global organization. The first major and long-term project is to implement Data Integrity activities together with our business partners within IT, Automation and in Line of Business. Great opportunity within Project Management, Quality and Data Integrity Your primary focus will be on further improving compliance within our GxP regulated IT and Automation systems locally as well as globally in LEO Pharma. You will play a key role in implementing Data Integrity activities across LEO Pharma ensuring that we uphold our License to Operate. Your primary responsibility will be: Drive the Data Integrity project together with the Data Integrity Lead and ensure progress on activities and on-time project deliveries Arrange and facilitate workshops within Data Integrity Train relevant employees in Data Integrity together with colleagues from Global Quality Ensure right level of documentation and compliance Maintain project plans and scope Report on project status Manage risks and issues proactively Manage resources and ensure allocation Other strategic projects are available in our pipeline and based on your competences, you will have the opportunity to drive multiple projects and get the chance to learn more about other areas within Global Quality CI. The ideal candidate To be successful in this role it is important that you have some knowledge of Data Integrity and is capable of challenging and supporting the organization in good collaboration. The ideal candidate is a team player with strong collaboration skills, outgoing, tolerant and open-minded. You have a can-do attitude and are responsible and flexible. Your experience and competences Minimum of 5 years experience within project management You have experience working with IT compliance within the pharmaceutical industry and have knowledge of Data Integrity requirements outlined by regulatory authorities Excellent facilitating skills with experience in executing workshops comprising 3-10 people Excellent stakeholder management skill Master of Science in e.g. Pharmacy, Engineering, IT and preferably in combination with project management training certification Good communication skills (English and Danish Scandinavian) 5-10 years of experience in a GxP regulated industry is expected Preferably LEAN experience or experience with continuous improvements Join our mission to help more people achieve healthy skin Hundreds of millions of people around the globe are suffering from an untreated skin disease. Helping these people to get a better life is what LEO Pharma is all about. By understanding their needs and wishes we will improve existing treatments and break new land to uncover the solutions of tomorrow. By joining LEO Pharma you will get the opportunity to create results, develop yourself among highly skilled colleagues while taking on our quest to become the preferred dermatology care partner improving people s lives around the world and at the same time create profitable growth. Contact and application The position is based at HQ in Ballerup in Global Quality Projects with employees located at all manufacturing sites across LEO. Most of your stakeholders will be in Ballerup, but some travel should be expected to our sites in Ireland and France. You should expect approx. 10-20 travel days a year. In case you have any questions, do not hesitate to contact Senior Manager Frederik Strecker Kruse, 45 3112 0455. We look forward to receiving your application. Deadline for submitting your application is August 4th 2019. Job interviews will be held on a continuous basis, so please submit your application as soon as possible.

This is your chance to join one of the world’s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. Global Quality Projects is responsible for project management within Global Quality & CI in LEO Pharma and we are looking for an experienced Project Manager to drive global quality projects in a global organization. The first major and long-term project is to implement Data Integrity activities together with our business partners within IT, Automation and in Line of Business.

Great opportunity within Project Management, Quality and Data Integrity

Your primary focus will be on further improving compliance within our GxP regulated IT and Automation systems locally as well as globally in LEO Pharma. You will play a key role in implementing Data Integrity activities across LEO Pharma ensuring that we uphold our License to Operate. Your primary responsibility will be:

  • Drive the Data Integrity project together with the Data Integrity Lead and ensure progress on activities and on-time project deliveries
  • Arrange and facilitate workshops within Data Integrity
  • Train relevant employees in Data Integrity together with colleagues from Global Quality
  • Ensure right level of documentation and compliance
  • Maintain project plans and scope
  • Report on project status
  • Manage risks and issues proactively
  • Manage resources and ensure allocation

Other strategic projects are available in our pipeline and based on your competences, you will have the opportunity to drive multiple projects and get the chance to learn more about other areas within Global Quality & CI.

 
The ideal candidate

To be successful in this role it is important that you have some knowledge of Data Integrity and is capable of challenging and supporting the organization in good collaboration.

The ideal candidate is a team player with strong collaboration skills, outgoing, tolerant and open-minded. You have a can-do attitude and are responsible and flexible.

 Your experience and competences

  • Minimum of 5 years’ experience within project management
  • You have experience working with IT compliance within the pharmaceutical industry and have knowledge of Data Integrity requirements outlined by regulatory authorities
  • Excellent facilitating skills with experience in executing workshops comprising 3-10 people
  • Excellent stakeholder management skill
  • Master of Science in e.g. Pharmacy, Engineering, IT and preferably in combination with project management training/certification
  • Good communication skills (English and Danish/Scandinavian)
  • 5-10 years of experience in a GxP regulated industry is expected
  • Preferably LEAN experience or experience with continuous improvements

Join our mission to help more people achieve healthy skin

Hundreds of millions of people around the globe are suffering from an untreated skin disease. Helping these people to get a better life is what LEO Pharma is all about. By understanding their needs and wishes we will improve existing treatments and break new land to uncover the solutions of tomorrow. 

By joining LEO Pharma you will get the opportunity to create results, develop yourself among highly skilled colleagues while taking on our quest to become the preferred dermatology care partner improving people’s lives around the world and at the same time create profitable growth.

 
Contact and application

The position is based at HQ in Ballerup in Global Quality Projects with employees located at all manufacturing sites across LEO. Most of your stakeholders will be in Ballerup, but some travel should be expected to our sites in Ireland and France. You should expect approx. 10-20 travel days a year.

In case you have any questions, do not hesitate to contact Senior Manager Frederik Strecker Kruse, +45 3112 0455.

We look forward to receiving your application. Deadline for submitting your application is August 4th 2019.

Job interviews will be held on a continuous basis, so please submit your application as soon as possible.

LEO PHARMA A/SBallerup2019-07-11T00:00:002019-08-04T00:00:00
330058553Project Manager/Analytical Coordinator with tech transfer experienceRobot Are you passionate about improving lives of millions of people by supporting all our marketed products? This is your chance to join one of the world s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. Global Research and Development in LEO Pharma devotes its efforts to develop innovative drugs for the treatment of skin diseases like psoriasis and eczema. You can look forward to becoming part of a team with high professional standards in an informal atmosphere where tasks vary, and no days are alike. Great opportunity within project management, analytical support and stability Pharmaceutical Product Support Area is part of Global R D, counting 40 persons divided into three departments. We provide fast, efficient and qualified pharmaceutical documentation and analytical support for all marketed products at LEO Pharma. You will join 12 enthusiastic and dedicated colleagues in the CMC Stability Support department in Pharmaceutical Product Support. Our focus is on LEO Pharma marketed products, and we provide support for stability studies, analytical and chemical trouble shooting, technical transfer of analytical methods and documentation. You will be part of a product group and will be responsible for a minor portfolio of products (primary small molecules), together with scientists from the CMC MA Support department. Our values are impact, courage, trust and mutual respect and helpfulness and we care about each other. As a support area, Pharmaceutical Product Support receives a large number of unforeseen and urgent enquiries, and you must therefore be able to juggle a number of tasks and work on several projects at the same time. Primary areas of responsibility: You will have a combined responsibility as project manager for various smaller and larger projects supporting CMC aspects of either Enstilar(R) manufacturing, or integration activities for our newly acquired Bayer dermatology portfolio along with scientific tasks within the department´s responsibilities for technical transfer of analytical methods, analytical support, set-up and evaluation of stability studies, OOS and OOT resolution, support during Health Authorities inspections and to some extent life cycle management activities and maintenance of regulatory documentation. As a part of your daily tasks you will be expected to perform: project management e.g. coordination of analytical method transfer, OOS resolutions analytical transfer documentation manage and participate in projects across the LEO organization globally stability evaluation of marketed products collaborate with CMO´s and CRO´s globally leading and participating in solving different analytical or production issues by identifying root cause and implement corrective actions on OOS and OOT so the production can continue to release products to the markets. to plan and execute analytical development and support to prepare analytical validations and investigations leading improvement projects and cross functional projects to some extent - write and update quality documentation for regulatory purposes in connection with maintenance, projects, questions from authorities, renewals and applications. The ideal candidate: The ideal candidate is a team player with strong collaboration skills, outgoing, tolerant and open-minded. You have a can-do attitude and are responsible, flexible, and a competent decision-maker. Your experience and competences: Minimum of 2 years experience as project manager analytical coordinator, including experience with technical transfer of analytical methods Excellent stakeholder management skills and experience in working in multi-cultural project teams You have experience working with CMO´s CRO´s and have the competencies to create a good collaboration Master of Science in e.g. Pharmacy, Engineering or Chemistry and preferably in combination with a PhD. You are capable of analyzing and reducing complex issues and you are a person who thrives in significantly improving, changing or adapting existing processes, systems or products Minimum of 5 years of experience within analytical chemistry and stability testing, strong CMC understanding, including insight in development, validation and implementation of HPLC methods and relevant statistical tools Good communication skills (English and Danish Scandinavian) A solid experience with GMP will be considered an advantage as we work in accordance with current GMP regulations Experience with regulatory requirements, pharmacopoeias and guidelines Preferably LEAN experience or experience with continuous improvements Further information Please be aware that due to the collaboration with CMO´s, CRO`s and other LEO production sites up to 4 weeks per year of travelling can be expected. Do not hesitate to contact Senior Manager Birthe Ross, 45 5365 4753 if you want to know more about the position. We look forward to receiving your application. Deadline is 17th August 2019. Job interviews will be held on a continuous basis.

Are you passionate about improving lives of millions of people by supporting all our marketed products?

This is your chance to join one of the world’s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. Global Research and Development in LEO Pharma devotes its efforts to develop innovative drugs for the treatment of skin diseases like psoriasis and eczema. You can look forward to becoming part of a team with high professional standards in an informal atmosphere where tasks vary, and no days are alike.

 

Great opportunity within project management, analytical support and stability

Pharmaceutical Product Support Area is part of Global R&D, counting 40 persons divided into three departments. We provide fast, efficient and qualified pharmaceutical documentation and analytical support for all marketed products at LEO Pharma.

You will join 12 enthusiastic and dedicated colleagues in the CMC Stability Support department in Pharmaceutical Product Support. Our focus is on LEO Pharma marketed products, and we provide support for stability studies, analytical and chemical trouble shooting, technical transfer of analytical methods and documentation. You will be part of a product group and will be responsible for a minor portfolio of products (primary small molecules), together with scientists from the CMC MA Support department. Our values are impact, courage, trust and mutual respect and helpfulness – and we care about each other. As a support area, Pharmaceutical Product Support receives a large number of unforeseen and urgent enquiries, and you must therefore be able to juggle a number of tasks and work on several projects at the same time.

Primary areas of responsibility:

You will have a combined responsibility as project manager for various smaller and larger projects supporting CMC aspects of either Enstilar(R) manufacturing, or integration activities for our newly acquired Bayer dermatology portfolio along with scientific tasks within the department´s responsibilities for technical transfer of analytical methods, analytical support, set-up and evaluation of stability studies, OOS and OOT resolution, support during Health Authorities inspections and to some extent life cycle management activities and maintenance of regulatory documentation.

 

As a part of your daily tasks you will be expected to perform:

  • project management e.g. coordination of analytical method transfer, OOS resolutions
  • analytical transfer documentation
  • manage and participate in projects across the LEO organization globally
  • stability evaluation of marketed products
  • collaborate with CMO´s and CRO´s globally
  • leading and participating in solving different analytical or production issues by identifying root cause and implement corrective actions on OOS and OOT so the production can continue to release products to the markets.
  • to plan and execute analytical development and support
  • to prepare analytical validations and investigations
  • leading improvement projects and cross functional projects
  • to some extent - write and update quality documentation for regulatory purposes in connection with maintenance, projects, questions from authorities, renewals and applications.

 

The ideal candidate:

The ideal candidate is a team player with strong collaboration skills, outgoing, tolerant and open-minded. You have a can-do attitude and are responsible, flexible, and a competent decision-maker.

 

Your experience and competences:

  • Minimum of 2 years’ experience as project manager/analytical coordinator, including experience with technical transfer of analytical methods
  • Excellent stakeholder management skills and experience in working in multi-cultural project teams
  • You have experience working with CMO´s/CRO´s and have the competencies to create a good collaboration
  • Master of Science in e.g. Pharmacy, Engineering or Chemistry and preferably in combination with a PhD. You are capable of analyzing and reducing complex issues and you are a person who thrives in significantly improving, changing or adapting existing processes, systems or products
  • Minimum of 5 years of experience within analytical chemistry and stability testing, strong CMC understanding, including insight in development, validation and implementation of HPLC methods and relevant statistical tools
  • Good communication skills (English and Danish/Scandinavian)
  • A solid experience with GMP will be considered an advantage as we work in accordance with current GMP regulations
  • Experience with regulatory requirements, pharmacopoeias and guidelines
  • Preferably LEAN experience or experience with continuous improvements

 

Further information

Please be aware that due to the collaboration with CMO´s, CRO`s and other LEO production sites up to 4 weeks per year of travelling can be expected. 

Do not hesitate to contact Senior Manager Birthe Ross, +45 5365 4753 if you want to know more about the position.

We look forward to receiving your application. Deadline is 17th August 2019.

Job interviews will be held on a continuous basis.

LEO PHARMA A/SBallerup2019-07-11T00:00:002019-08-17T00:00:00
330058150Ambitious Senior Project Manager to Technology innovationRobot Are you ready for a position with impact on the future of Novo Nordisk? Do you have what it takes to keep major projects on track and lead your team members to success? Do you have a scientific background and a strong track record managing complex projects? If so, we can offer you a rarely posted position, where research, development and production come together, and where your work will be changing the lives of millions of people living with diabetes now and in the future. About the department Diabetes Manufacturing Development (MDev) is where our cutting-edge research is transformed to actual production of life-changing medicine. Here we strive to improve the production and analysis process, all to secure stabile delivery of high quality products in regulatory compliance to our more than 24 million patients all over the world. We are app. 300 project managers, chemists, laboratory technicians and specialists all coming together to change diabetes. We lead complex, cross-organisational optimisation projects improving existing processes and analytical methods. These projects typically aim to reduce costs, expand production capacity and improve the quality of our finished products. You will be part of the MDev Technology Innovation - a group of 15 innovative and dedicated colleagues. The department is a major player in providing disruptive technology solutions to overcome key business challenges focusing in enabling DFP to prepare for the future technology - we drive the projects that define the future production in Novo Nordisk. We are working with a very open mind-set and are collaborating with academia s, start-ups, technology providers and innovation houses in order to bring new technology into Diabetes Finished Production to support following focus areas: Zero human interventions in Aseptic Production. The position As a senior project manager, you will be responsible for managing projects with high complexity within technology innovation in general. Specifically drive projects that support the vision on removing people from Class A during filling operation in Aseptic production. This is done by continuously evaluate ideas and external technologies for potential to enter the relevant project model. You will need to set direction for initiated projects, negotiate project resources with LoB management and manage these resources during project execution. Together with key project members, you will create innovative concepts that can be piloted on a production site and matured to be ready for scale up and global roll out. You will be collaborating with various external as well as internal partners on the projects, people with different backgrounds, across organisational levels and geography. The job will be performed primarily from Denmark with expected around 10 of travel. Qualifications We expect you to have a MSc level education from the life sciences maybe you hold a degree in engineering Cand. Scient. Or another relevant background with at least 7 years relevant working experience. Most importantly, you can demonstrate a convincing project management track record with impressive results from at least four years of experience managing cross-organisational projects with high levels of complexity. You have an innovative mind-set and are open for thinking completely different and challenge status quo. Deep subject matter experience within aseptic production in a GMP environment is preferred. As a Senior Project Manager, you rely on many personal qualifications and skills to succeed. You are capable of creating a shared vision for the project team, and you can get your team members to commit to the details of your project plan. You know how to motivate your team members when difficult challenges arise, and your can-do attitude is reflected by everyone involved in the projects you lead. You convey your authority effortlessly, and you earn the trust and respect of the people you work with by leading by example. You like to work across different fields of expertise and you throw yourself at opportunities for expanding your knowledge and skills. You pro-actively prevent problems before they emerge - your strong analytical mind allow you to think several steps ahead and anticipate any issues that might challenge the advancement of the project. Your strong communication skills and your empathic approach to people make it easy for you to build and maintain trustful relations both within your department and to all the stakeholders you will be working with. Working at Novo Nordisk Novo Nordisk Manufacturing is a market-leading, global company. We know success depends on dedicated individuals contributing to every step of the way. The empowerment of all employees is our top priority, and we actively support your individual career development. Solid and constant high performance in a business like ours, leads to a wide range of career opportunities. Your next step is up to you! Contact If you have questions about the position, you are welcome to call Rune Funder Hansen at 45 3075 3790. Deadline July 28th 2019 Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Are you ready for a position with impact on the future of Novo Nordisk? Do you have what it takes to keep major projects on track and lead your team members to success? Do you have a scientific background and a strong track record managing complex projects? If so, we can offer you a rarely posted position, where research, development and production come together, and where your work will be changing the lives of millions of people living with diabetes – now and in the future.

 

About the department

Diabetes Manufacturing Development (MDev) is where our cutting-edge research is transformed to actual production of life-changing medicine. Here we strive to improve the production and analysis process, all to secure stabile delivery of high quality products in regulatory compliance to our more than 24 million patients all over the world. We are app. 300 project managers, chemists, laboratory technicians and specialists – all coming together to change diabetes. 

We lead complex, cross-organisational optimisation projects improving existing processes and analytical methods. These projects typically aim to reduce costs, expand production capacity and improve the quality of our finished products. 

You will be part of the MDev Technology Innovation - a group of 15 innovative and dedicated colleagues. The department is a major player in providing disruptive technology solutions to overcome key business challenges focusing in enabling DFP to prepare for the future technology - we drive the projects that define the future production in Novo Nordisk. 

We are working with a very open mind-set and are collaborating with academia’s, start-ups, technology providers and innovation houses in order to bring new technology into Diabetes Finished Production to support following focus areas: Zero human interventions in Aseptic Production.

 

The position

As a senior project manager, you will be responsible for managing projects with high complexity within technology innovation in general. Specifically drive projects that support the vision on removing people from Class A during filling operation in Aseptic production. This is done by continuously evaluate ideas and external technologies for potential to enter the relevant project model. You will need to set direction for initiated projects, negotiate project resources with LoB management and manage these resources during project execution.

Together with key project members, you will create innovative concepts that can be piloted on a production site and matured to be ready for scale up and global roll out. 

You will be collaborating with various external as well as internal partners on the projects, people with different backgrounds, across organisational levels and geography. The job will be performed primarily from Denmark with expected around 10% of travel.

 

Qualifications

We expect you to have a MSc level education from the life sciences – maybe you hold a degree in engineering Cand. Scient. Or another relevant background with at least 7 years relevant working experience. Most importantly, you can demonstrate a convincing project management track record with impressive results from at least four years of experience managing cross-organisational projects with high levels of complexity. You have an innovative mind-set and are open for thinking completely different and challenge status quo. Deep subject matter experience within aseptic production in a GMP environment is preferred. 

As a Senior Project Manager, you rely on many personal qualifications and skills to succeed. You are capable of creating a shared vision for the project team, and you can get your team members to commit to the details of your project plan. You know how to motivate your team members when difficult challenges arise, and your can-do attitude is reflected by everyone involved in the projects you lead. You convey your authority effortlessly, and you earn the trust and respect of the people you work with by leading by example. 

You like to work across different fields of expertise and you throw yourself at opportunities for expanding your knowledge and skills. 

You pro-actively prevent problems before they emerge - your strong analytical mind allow you to think several steps ahead and anticipate any issues that might challenge the advancement of the project. 

Your strong communication skills and your empathic approach to people make it easy for you to build and maintain trustful relations – both within your department and to all the stakeholders you will be working with.

 

Working at Novo Nordisk

Novo Nordisk Manufacturing is a market-leading, global company. We know success depends on dedicated individuals contributing to every step of the way. The empowerment of all employees is our top priority, and we actively support your individual career development. Solid and constant high performance in a business like ours, leads to a wide range of career opportunities. Your next step is up to you!

 

Contact

If you have questions about the position, you are welcome to call Rune Funder Hansen at +45 3075 3790.

 

Deadline

July 28th 2019

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

NOVO NORDISK A/SBagsværd2019-07-10T00:00:002019-07-28T00:00:00
330058145Global Project Manager in Medical Affairs (maternity cover)Robot We are recruiting for a Global Project Manager on the Scientific Dialogue team, Global Medical Affairs (Søborg, Denmark). You can look forward to an exciting job leading projects and engaging with multiple stakeholders at the global and local level. This is a fixed term position to cover a maternity leave (14 months, incl. handover period). About the department You get the opportunity to join an international, high performing team with a variety of backgrounds (project management, communication, marketing and international business). We use our differences to create novel ideas and high-quality solutions. In Scientific Dialogue, we drive global medical education initiatives as well as engagement planning for Key Opinion Leaders Health Care Professionals. Moreover, we collaborate with key affiliates and global stakeholders to ensure continuous improvement of the Medical Affairs function globally and strive for excellence in all we do. The position As a Global Project Manager, you will be responsible for driving the execution and follow-up of scientific meetings and events that aim to engage Health Care Professional in impactful scientific dialogue to improve outcomes for people with diabetes, obesity and cardiovascular disease. You will work in close collaboration with the internal Medical Affairs team, selected affiliates, and external agencies to drive the successful execution of programmes across countries and audiences. You will be responsible for communicating program achievements in an impactful way to relevant stakeholders. In addition, you will collaborate with internal and external stakeholders to innovate the design and delivery of medical education and scientific programs, implement new approaches to programme evaluation, and ensure effective communication to relevant stakeholders about the impacts realised by a portfolio of training and learning activities. Qualifications We are looking for a Global Project Manager who is passionate about project management and communication. You have a Master s degree in Business, Communication, Global Health, Education, or other related fields and 2 to 4 years of relevant experience with cross-functional project management. Experience working with event management, medical education, and impact evaluation. You are fluent in both oral and written English, you are able to manage several projects at the same time and take a methodical approach to your work and tasks but demonstrate flexibility when priorities change. This position may require up to 30 travel days annually. In addition, you bring a can-do attitude and a healthy sense of humour to your work even when the pressure is on. Finally, you have excellent interpersonal skills and a professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Michael Calopietro at 45 3077 6539. Deadline 26 July 2019. Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

We are recruiting for a Global Project Manager on the Scientific Dialogue team, Global Medical Affairs (Søborg, Denmark). You can look forward to an exciting job leading projects and engaging with multiple stakeholders at the global and local level. This is a fixed term position to cover a maternity leave (14 months, incl. handover period).

 

About the department

You get the opportunity to join an international, high performing team with a variety of backgrounds (project management, communication, marketing and international business). We use our differences to create novel ideas and high-quality solutions. In Scientific Dialogue, we drive global medical education initiatives as well as engagement planning for Key Opinion Leaders & Health Care Professionals. Moreover, we collaborate with key affiliates and global stakeholders to ensure continuous improvement of the Medical Affairs function globally and strive for excellence in all we do.

 

The position

As a Global Project Manager, you will be responsible for driving the execution and follow-up of scientific meetings and events that aim to engage Health Care Professional in impactful scientific dialogue to improve outcomes for people with diabetes, obesity and cardiovascular disease. You will work in close collaboration with the internal Medical Affairs team, selected affiliates, and external agencies to drive the successful execution of programmes across countries and audiences. You will be responsible for communicating program achievements in an impactful way to relevant stakeholders. 

In addition, you will collaborate with internal and external stakeholders to innovate the design and delivery of medical education and scientific programs, implement new approaches to programme evaluation, and ensure effective communication to relevant stakeholders about the impacts realised by a portfolio of training and learning activities.

 

Qualifications

We are looking for a Global Project Manager who is passionate about project management and communication. You have a Master’s degree in Business, Communication, Global Health, Education, or other related fields and 2 to 4 years of relevant experience with cross-functional project management. Experience working with event management, medical education, and impact evaluation. You are fluent in both oral and written English, you are able to manage several projects at the same time and take a methodical approach to your work and tasks but demonstrate flexibility when priorities change. This position may require up to 30 travel days annually. 

In addition, you bring a can-do attitude and a healthy sense of humour to your work even when the pressure is on. Finally, you have excellent interpersonal skills and a professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects.

 

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

 

Contact

For further information, please contact Michael Calopietro at +45 3077 6539.

 

Deadline

26 July 2019.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Novo Nordisk A/SSøborg2019-07-10T00:00:002019-07-26T00:00:00
da-DK

Andre job der matcher din søgning

Senior Clinical Project Manager

LEO PHARMA A/S

Ballerup
Would you like to play a key role in the development of our growing portfolio together with a friendly, ambitious and professional team in Trial Management? You will join a very successful company, dedicated towards fulfilling the vision of becoming...
Indrykket:11. juli 2019
Udløbsdato:15. august 2019

Project Manager with Quality experience

LEO PHARMA A/S

Ballerup
This is your chance to join one of the world s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. Global Quality Projects is responsible for project management within Global Qu...
Indrykket:11. juli 2019
Udløbsdato:4. august 2019

Project Manager/Analytical Coordinator with tech transfer experience

LEO PHARMA A/S

Ballerup
Are you passionate about improving lives of millions of people by supporting all our marketed products? This is your chance to join one of the world s leading companies within dermatology and to set your mark on the quality of life for millions of p...
Indrykket:11. juli 2019
Udløbsdato:17. august 2019

Ambitious Senior Project Manager to Technology innovation

NOVO NORDISK A/S

Bagsværd
Are you ready for a position with impact on the future of Novo Nordisk? Do you have what it takes to keep major projects on track and lead your team members to success? Do you have a scientific background and a strong track record managing complex p...
Indrykket:10. juli 2019
Udløbsdato:28. juli 2019

Global Project Manager in Medical Affairs (maternity cover)

Novo Nordisk A/S

Søborg
We are recruiting for a Global Project Manager on the Scientific Dialogue team, Global Medical Affairs (Søborg, Denmark). You can look forward to an exciting job leading projects and engaging with multiple stakeholders at the global and local level....
Indrykket:10. juli 2019
Udløbsdato:26. juli 2019