Manager for CMC Shipping, Quality & Training
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Søborg
Ready to join a business area that ensures the success and integrity of Active Pharmaceutical Ingredients (API) processes in Managing shipments of Intermediates, APIs and Drug Products to and from CMOs to support our growing development pipeline. Oversee the Quality Management System (QMS) in CMC API Development. Lead training initiatives across CMC API Development. Excel in internal/external stakeholder management, setting up collaboration and support processes. Empower, motivate, and develop employees to secure high team performance. Closely collaborating with the Shipping team in USA. To succeed in this position, you will act with a strong optimising mindset to secure continuous workflow and efficiency. Furthermore, lead as a role model embracing an open, visible and respectful approach and place the well-being of your team as a key priority by building a trustful and vibrant working environment.You will be a part of the CMC API Process Development leadership team of 9 Managers and direct reference to the Senior Director heading up the department.QualificationsPreferably, you have a master’s degree (MSc) or PhD in engineering, biochemistry/chemical engineering, pharmacy, or other relevant fields. Furthermore, you have:A minimum of +5 years of people management, ideally from the pharmaceutical industry or production environment. Passionate about motivating and developing your team members. Pay credit where credit is due. Experience from a GMP-regulated area is highly advantageous. The ability to challenge the status quo and see cLEAN as a natural part of your daily work. Good communication skills in Danish and English As a leader, you demonstrate authenticity and inspire and motivate others to achieve high-quality results, uniting people and creating followership. You demonstrate strong communication skills and take responsibility for driving an agenda where tasks and activities are in flow.On a personal level, you are motivated in seeing people and processes develop, enjoy supporting across the organisation and thrive in multiple agendas prioritizing to finds simple solutions to complex challenges.About the departmentAs part of Product Supply organisation, CMC Product & Process Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set.The CMC API Process Operations department is approx. 100 employees dedicated to support the development of API within . The department is comprised of 9 specialised teams, each contributing critical expertise to ensure the success and integrity of our API processes e.g. within GMP materials, Virology & Cell Banks, CMC shipping, API QMS and digital development.Working at is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 60,000 employees. Together, we go further. Together, we’re life changing.ContactFor further information, please feel free to contact Senior Director, Mark Bonefeld Nielsen on + .Deadline21st of April 2025.Due to short deadline, we encourage you to apply as fast as possible.Please note that we will review applications and call in for interviews continuously.You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV.We 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.
development projects? Curious about working in the intersection of shipping, quality and training disciplines in an API development context? Are you a robust leader who knows how to lead and harness your teams’ capabilities through strong collaboration and active stakeholder management?If yes, we are looking for an experienced leader to join our Shipping, Quality & Training team in Chemistry, Manufacturing and Control (CMC) API Process Operations to lead and develop the team and to further strengthen and build on our well-functioning processes.This is your opportunity to grow personally and professionally by developing your leadership competencies in a well-established department setting the highest standards of quality and safety. Come join us for a life-changing career and apply today!The positionCMC API Process Operations is a multidisciplinary department responsible for the majority of good manufacturing practice (GMP) API processes in the CMC API Development area. We have the responsibility from pre-clinic/phase 1 to phase 3 and have stakeholders across multiple divisions as well as externally globally.As we support more and more pipeline projects with outsourcing activities, the CMC Shipping agenda continues to grow. Similarly, the quality and training agenda are also evolving as integration of foreign sites and new drug modalities are entering CMC.As Manager for the CMC Shipping, Quality & Training team, you will lead a team of 15 employees (Scientists, Pharmaceutical Logistic Coordinators, QMS Professionals etc.) responsible for preparing, executing, and handling our +500 yearly shipments to and from Contract Manufacturing Organisations (CMO) globally, while overseeing our internal/external quality and training.As Manager you will be:
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 8.4.2025, 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.
- 08.04.2025
- Øvrige
- Søborg
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