GMP Compliance Partner
Novo Nordisk
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 Novo Nordisk!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 managementTaking part in managing the department regarding GMP, setting direction, and driving actions and projects across the departmentMoreover, 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 fieldAt 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 processesThe ability to think and act with a broad perspective, encompassing the big picture while maintaining focus on and interest in crucial detailsProfessional proficiency in both Danish and EnglishAs 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.
Hillerød, Hovedstaden
Sat, 15 Jun 2024 22:43:32 GMT
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