Senior QA Manager for Drug Substance Projects
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Søborg
Are you looking for your next leadership position in an international environment? Are you motivated by having challenges with huge business impact requiring a high level of professional QA competencies and leadership experience to bring benefits to our patients and stakeholders? If yes, then you might be our new Senior QA Manager for Drug Substance Projects we are looking for to take a leading role where efforts can make a positive and direct difference every day. Apply now and be part of a life-changing career!
The position As Senior QA Manager you will be heading up the Global Contact Manufacturing (GCM) QA Drug Substance Projects team consisting of highly trained and experienced QA professionals and specialists who all have important roles in the tech transfer, process validation and implementation of new Contract Manufactures (CMOs) in close collaboration with peers in GCM and other internal stakeholders. You will drive the overall QA agenda in various outsourcing projects of Drug Substance and starting materials production processes, with a high level of complexity and independent decision making in your daily tasks. Since you will be working in a global environment, you will get the opportunity to travel to CMO partners globally for approximately 30 days per year. In your role, you will report to the QA Vice President and become a member of the GCM QA management team. Among your key responsibilities, you will: Leading, developing and shaping the team in alignment with quality requirements and constantly changing business needs Warranting stable and robust internal processes in compliance with GMP requirements Driving the quality culture in close collaboration with our stakeholders within the projects Ensuring we never compromise on quality and quality compliance of outsourced products in close collaboration with the CMO QA functions Qualifications We are looking for a strong leader with QA background and insights in the pharmaceutical industry, with ability to balance quality, delivery, and cost. To succeed in this role, you have: M.Sc. degree in pharmacy, engineering or similar Substantial experience in quality assurance from pharmaceutical production and a deep insight in the GMP regulations, especially validation requirements Great leader and people management skills with a long track record Strong written and spoken English knowledge Drug substance manufacturing experience On a personal note, you have a visible leadership style, and you can listen, coach and motivate your employees to deliver their best. You seek influence in quality matters and are comfortable being challenged by senior stakeholders. Your high level of personal integrity and robustness enables you to integrate different views in the decision-making process. Having said that, we expect you can stay firm when needed to secure the quality and compliance aspects. Last but not least, you are well organised and create strong results by engaging your employees in taking pride in delivering on their objectives. About the area GCM QA are responsible for product quality and QA Oversight of CMOs and the final batch release of batches produced externally. Currently the department consists of 60+ highly qualified employees in 5 different teams, but we are growing very fast and expecting to become bigger in the nearest future. We are working in an international environment with many different companies and stakeholders with engagement, trust and mutual respect. Our performance is driven by the right behavioural and a wish to think big, improve and simplify our way of working while ensuring quality compliance, product quality and patient safety. Working at Novo Nordisk At Novo Nordisk, 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 Arslan Nejadi, Vice President at +45-34485718. Deadline 01 October 2023 Please be advised that interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible. 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 in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk 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.
The position As Senior QA Manager you will be heading up the Global Contact Manufacturing (GCM) QA Drug Substance Projects team consisting of highly trained and experienced QA professionals and specialists who all have important roles in the tech transfer, process validation and implementation of new Contract Manufactures (CMOs) in close collaboration with peers in GCM and other internal stakeholders. You will drive the overall QA agenda in various outsourcing projects of Drug Substance and starting materials production processes, with a high level of complexity and independent decision making in your daily tasks. Since you will be working in a global environment, you will get the opportunity to travel to CMO partners globally for approximately 30 days per year. In your role, you will report to the QA Vice President and become a member of the GCM QA management team. Among your key responsibilities, you will:
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 15.5.2023, 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.
- Øvrige
- Søborg
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