QMS and Training Professional
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Are you curious to use your quality knowledge, experience, and mindset in an exciting organization and are you passionate about shaping effective training strategies tailored to business needs? Do you have a systematic approach and perform first class stakeholder management? Would you enjoy being responsible for setting the quality agenda and to drive training-related improvement projects and elevate training standards across the department?
If yes, then apply now to make a transformative impact as our new QMS and Training Project Manager.
The PositionAs Quality Management System (QMS) & Training Project Manager you will play a central role in ensuring the most effective, efficient and compliant training and secure a high level of quality and compliance standard across CMC Bioanalysis. You will be working to ensure a high level of quality and compliance, by setting the right strategy and standards in maintaining our QMS so that we continuously deliver on all relevant GMP requirements and secure training-related competence development.
Main tasks will include:Be the go-to person on quality and training-related subjects; you actively identify and drive quality- and training improvement initiatives, and support as needed by applying systematic problem-solving, process mapping, or other LEAN methodologies
Ensuring high-level GMP overview and report quality trends to management
Driving preparation for, participate in and follow-up on authority inspections and internal audits
Supporting daily operations and ensure the relevant level of GMP and training
Support management in ensuring effective, efficient and compliant training and competence development set-up best suited for the business area
Identifying needs for optimization and improvement in training setups both locally and across entire CVP area
You will work closely with the entire GMP network both locally and on a global level, and your stakeholders at CVPs and QMS partner level
Identify and drive locally quality improvement initiatives by applying systematic problem-solving, process mapping, or other cLEAN tools
Qualifications We envision to welcome a colleague with Project Management-, QMS and GMP knowledge who is not afraid to challenge the status quo and is ready to revolutionize the way we work, aiming to drive to new and exciting goals while ensuring we maintain the highest quality standards.To succeed in this role, you have:A master’s degree or PhD in pharmacy, biochemistry, production engineering or similar
Extensive experience from the pharmaceutical industry, as QMS, GMP or QA specialist or similar
Experience with project management and LEAN
Full professional proficiency Danish and English
On a personal level you thrive and get motivated by working with and across all levels in the organization, whilst you enjoy great collaboration and communication and setting direction. Additionally, you are solution oriented and work systematically with a pragmatic approach and strive for simplicity in processes.
About The DepartmentThe Bioanalysis Department is part of CMC Analysis and Characterization. We support and develop analysis for the analysis of samples from 's entire project portfolio. We are characterized by always delivering on time with high quality, as well as being front runners in new technology and innovative solutions.
The department is divided into three teams, and you will be anchored in the Binding Assay team, however supporting the entire department. We are a department with great experience in bioanalyses, and where the tasks continuously change in nature in line with new development projects and the project portfolio. We are characterized by and proud of preserving the team spirit and can-do attitude, which enables us to make a difference for patients all over the world.
ContactIf you want to hear more or have questions, please do not hesitate to contact our Manager, Julie Goldenbaum by email: 21 April 2025We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
If yes, then apply now to make a transformative impact as our new QMS and Training Project Manager.
The PositionAs Quality Management System (QMS) & Training Project Manager you will play a central role in ensuring the most effective, efficient and compliant training and secure a high level of quality and compliance standard across CMC Bioanalysis. You will be working to ensure a high level of quality and compliance, by setting the right strategy and standards in maintaining our QMS so that we continuously deliver on all relevant GMP requirements and secure training-related competence development.
Main tasks will include:
About The DepartmentThe Bioanalysis Department is part of CMC Analysis and Characterization. We support and develop analysis for the analysis of samples from 's entire project portfolio. We are characterized by always delivering on time with high quality, as well as being front runners in new technology and innovative solutions.
The department is divided into three teams, and you will be anchored in the Binding Assay team, however supporting the entire department. We are a department with great experience in bioanalyses, and where the tasks continuously change in nature in line with new development projects and the project portfolio. We are characterized by and proud of preserving the team spirit and can-do attitude, which enables us to make a difference for patients all over the world.
ContactIf you want to hear more or have questions, please do not hesitate to contact our Manager, Julie Goldenbaum by email: 21 April 2025We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 7.4.2025, 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.
- 07.04.2025
- Øvrige
- Måløv
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