GMP VP Partner

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Gentofte

We are seeking an experienced candidate who is passionate about compliance, structure, and continuous improvement, and possesses a self-motivated, structured, and efficient nature. If you have a proven track record of identifying solutions in a broader perspective and setting clear direction and have demonstrated a commitment to making a significant difference, we want you! Apply now and join our team of seasoned professionals who are dedicated to changing lives through their work. The position As our new GMP VP Partner you will be a part of Biotech and Rare Disease, Aseptic Production (BRD AP) management group, referring to the VP. You will be responsible for supporting that the departments within BRD AP are continuously improving compliance and delivering on all relevant GMP requirements. The position also includes the coordination of audit and inspections across the whole CVP area of FP GEVA, being the one planning, organizing, and executing audits and inspections. You will also play an important role of supporting the GMP coordinators to ensure a high level of quality and compliance in our Aseptic Production area in Gentofte, by setting high standards, identifying, scoping, and driving compliance improvement initiatives while maintaining our Quality Management System (QMS). You will be responsible for:
  • Coordinating preparation for and follow-up on authority inspections and internal audits and providing ad hoc consultation on quality and compliance improvement ideas and challenges.
  • Supporting compliance with cGMP and NN QMS.
  • Developing and maintaining quality oversight systems to identify trends and propose relevant actions.
  • Ensuring high-level GMP overview and reporting quality trends to management
  • Driving continuous improvement of quality performance and processes.
    • As part of your key responsibilities, you will be responsible for ensuring the maintenance of a productive and efficient GMP coordinators network, which will facilitate collaboration, alignment, and the sharing of best practices for GMP-related tasks across BRD AP. Qualifications To qualify for this role, you should have:
  • A degree in a scientific field such as Pharmacy, Sciences, Engineering, or a similar discipline.
  • +5 years of experience in a similar position within GMP production.
  • A LEAN mindset with experience in systematic problem-solving.
  • Full proficiency in oral and written English.
  • Excellent interpersonal skills and proven experience in working with stakeholders at all levels.
    • Experience in Aseptic Production would be an advantage. As a person, you thrive on collaborating with individuals of all levels within the organization. You are known for your excellent communication and collaboration skills, and your ability to set direction. You are solution-oriented, and you work systematically and proactively while striving for simplicity in processes. You take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your stakeholders. About the department Our VP area is part of the BRD Finished Products Gentofte and Vaarloese area that is the production site situated close to Copenhagen. Here we are app. 725 colleagues who take responsibility for transforming Active Pharmaceutical Ingredients into the finished product that patients can use all over the world. We are producing at full speed on existing lines while building and ramping up new state of the art facilities. Our complex processes require a high level of expertise, commitment, and engagement from our employees and include formulation, filling, freeze-drying, product inspection, assembly, and pack. We bring value to patients by delivering high-quality Good Manufacturing Process (GMP) compliant products in a timely and cost-efficient manner. We drive change by working actively with LEAN and always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible Working at Novo Nordisk Novo Nordisk is all about its people. We understand that life is not always straightforward and balancing what is important at different stages of our career can be challenging. That's why we make room for diverse life situations and always put people first. We value our employees for the unique skills they bring to the table and continuously strive to bring out the best in them. Working at Novo Nordisk means working toward something bigger than ourselves, and it's a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we can go further. Together, we can change lives. Contact To learn more about this opportunity please call, Cecilie Moberg on +45 34 48 12 42. Deadline 24th of September 2023 Interviews will be held throughout the period, and 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.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Gentofte.

    Jobbet er oprettet på vores service den 13.7.2023, men kan have været deaktiveret og genaktiveret igen.

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