Team Lead for Clinical Supplies Development
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Are you an authentic and strong people leader, eager to set the direction through a team of specialised Project Professionals in Clinical Supplies? Are you eager to be part of an area, where develops and run clinical trials reaching more than 48.000 patients all over the world? Are you ready to play a pivotal role in making sure process development activities related to setting up future clinical trials are carried through and secured strong collaboration and stakeholder management? If leading, developing and the well-being of your team members is one of your core values, then you might be our new Team Lead (Associate Manager) to join our leadership team in Clinical Supplies (CS) Development. We have just had our 1-year anniversary in the new department CS Development and it’s time to establish the first team. We are looking for a passionate Associate Manager, who wants to make its mark on this new journey. T ake the next step in your life-changing career and a pply today! The position The department CS Development consist of about 15 employees, responsible for setting up new processes to handle what is needed to bring clinical supplies to clinical trials all over the world. We are a part of Chemistry, Manufacturing and Control (CMC) Clinical Supplies . CMC Clinical Supplies is a complete value chain from production to shipments to patients globally. As Associate Manager for CS Development, you will work closely together with the Director and create the perfect environment for your team. Your team consist of 8-10 employees that both handle projects to support that CMC Clinical Supplies is fit to run trials, but also have the responsibility of support processes that ensures that CMC Clinical Supplies can operate when using new products, e.g. new ways of handling secondary packing, blinding set up and much more. You will be responsible for setting up the structure for the team in line with our strategy and in a way where we can operate with focus on simplicity and productivity. We are a dynamic development environment, where sharp priorities are needed every day to reach more patients in the future. Your primary responsibility is to be visible, easy to approach as well as: set direction for the team both short and long term to ensure that all activities are planned and completed timely and in compliance with GMP/GCP standards. focus on maintaining a high level of drive and commitment in the team, through visible and authentic leadership. develop a culture where everyone is ready to challenge status quo, feel safe to speak up and where diversity of different thinking is appreciated. The support processes impact a lot of internal and external processes, hence a strong focus on stakeholder interaction and alignment is needed. As Associate Manager for CS Development you will be reporting to the Director of CS Development and be a part of the management team.
Qualifications To succeed in this role, you hold a MSc or other degree in a relevant field (e.g. engineering, supply chain, pharmacy). Furthermore, you will need: Several years of experience in people management, ideally within a development or production environment. Solid knowledge of pharmaceutical industry, Good Manufacturing Practice (GMP) and/or Good Clinical Practice (GCP) is an advantage. Familiar with various LEAN principles Strong communication skills in Danish and English, both written and spoken As a leader, you have a natural authenticity and a proven ability to inspire and motivate others to deliver high quality results. Through a structured approach you set and drive the direction and anchoring by seeking simple solutions and see continuous improvement as a natural part of your processes. As a person you possess strong interpersonal skills, which enables you to build trust within your team. You like to develop, involve, and empower your team members and can communicate and collaborate effectively across disciplines. You are a team player and find motivation when reaching common goals. About the department As part of PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling 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. Clinical Supplies Development is a part of Clinical Supplies in CMC Development & Scaling. CMC Clinical Supplies are responsible for ensuring that labelled and packed clinical trial products are available on time, in right quality and quantity for all clinical trials conducted by . Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Director Laila Baadsgaard +
Deadline 9th October 2024 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 facilitate an unbiased recruitment process, please refrain from adding a photo in 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.
Qualifications To succeed in this role, you hold a MSc or other degree in a relevant field (e.g. engineering, supply chain, pharmacy). Furthermore, you will need:
Deadline 9th October 2024 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 facilitate an unbiased recruitment process, please refrain from adding a photo in 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.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 17.9.2024, 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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