GMP Compliance Partner

Hillerød

Do you have a knowledge of the Good Manufacturing Practice (GMP), and are you motivated by setting high compliance standards and ensuring that we continuously improve our processes and ways of working? Are you excited about the possibility to work with highly qualified colleagues within pharmaceutical field?
If so, you might be our new GMP Compliance Partner in Filling & Inspection department in Hillerød, Denmark. Apply now and join [xxxxx]! The position
As the GMP Compliance Partner for the department, you will collaborate closely with the management team and supporters. Your primary role will involve supporting both management and colleagues in upholding and enhancing a high level of Good Manufacturing Practice (GMP).
Work tasks will include, but are not limited to:
  • Coaching and assisting your colleagues in GMP-related tasks such as deviations and changes (delimitation, corrective & preventive actions, qualification, etc.)

  • Maintaining a high-level GMP overview and reporting on GMP and quality trends to management

  • Taking part in managing the department regarding GMP, setting direction, and driving actions and projects across the department


  • Moreover, you will also be a member of the GMP network within the area. In collaboration with your peers in other departments, you will tackle tasks and challenges that span across different areas, such as inspection preparation, implementation of new systems or procedures, etc.
    Your job will be characterized by a dynamic blend of coordination, follow-up, and participation in management-related activities, alongside the focused execution of your own tasks. As a result, a flexible workstyle, and the ability to prioritize your tasks and time are essential qualities for this role. Qualifications
    We are looking for someone who proactively takes initiatives and secures commitment from the stakeholders. Our ideal candidate is focused on change management when introducing new ideas.
    To succeed in this role, we expect you to have:
  • An Academic Degree within pharmacy, engineering, or similar field

  • At least 3 years of experience in the pharmaceutical or medical device industry, or a related field, with a specific focus on GMP regulated areas and complex production processes

  • The ability to think and act with a broad perspective, encompassing the big picture while maintaining focus on and interest in crucial details

  • Professional proficiency in both Danish and English


  • As an individual, you radiate a positive, cooperative, action-oriented, and solution-focused approach. You work systematically, logically, and proactively. Your effective communication spans all levels of the organization, from operators to management, and you take pride in resolving tasks and challenges with a hands-on approach, involving key stakeholders closely in the process. About the department
    In Aseptic Production site Hillerød we are responsible for filling insulin on cartridges at highly automated and advanced equipment. We are proud to work in a newly established facility that supports the market with insulin to change living with diabetes for our patients.
    In Filling & Inspection we are dedicated to deliver strong results that add to the success of [xxxxx] in crucial ways by constantly improving our operational effectiveness and applying a strong lean operational system. We share a relaxed tone and high ambitions, and we are proud to never compromise on quality or safety.
    You will have the opportunity to develop professionally and personally in a new fast paced factory with great significance for the value chain of [xxxxx], high business complexity and competing interests. We believe in personal development and have high ambitions for our collaborative performance. Working at [xxxxx]
    At [xxxxx], we do not wait for change. We drive it. We are 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 are all working to move the needle on patient care. Contact
    For further information, please contact Director, AP Filling & Inspection, Peter Nøhr at +[xxxxx]or [xxxxx] Deadline
    30 June 2024.
    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 [xxxxx] 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 Hillerød.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • 14.06.2024
    • Øvrige
    • Hillerød