GMP Compliance Partner

Location:

Hillerød – Frederiksborg, Zealand, Denmark

Salary:

Competitive

Type:

Permanent

Main Industry:

Search Management & Executive Jobs

Other Industries & Skills: 

Manufacturing, Media

Job ID:

131224185

Posted On: 

13 October 2024

Join us as the GMP Compliance Partner in Filling & Inspection department in Hillerød and be at the forefront of our mission to uphold and elevate GMP standards. Collaborate with management, coach your colleagues, and lead impactful projects. Shape the future of our GMP practices with your expertise and drive for excellence.

The position
As the GMP Compliance Partner for our department, you will be at the heart of our mission to uphold and elevate our standards of Good Manufacturing Practice (GMP). Working hand-in-hand with the management team and dedicated supporters, your role will be pivotal in steering our commitment to excellence.

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
 

As a vital member of the GMP network within our area, you will join forces with peers from other departments to address various challenges. Your collaborative efforts will include preparing for inspections and implementing new systems or procedures, ensuring we stay ahead of industry standards.

Your role will be a dynamic mix of coordination, follow-up, and active participation in management activities, coupled with the focused execution of your tasks. This position calls for a flexible work style and exceptional prioritization skills to manage your time effectively.

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 Site Hillerød

Site Hillerød is an innovative and fast-growing production site. With over 4,000 talented employees, we work together to drive change for people living with serious chronic diseases. The site is located in beautiful natural surroundings, and we offer a diverse array of career paths at all educational levels. Join our vibrant community at Site Hillerød and ramp up your career while we ramp up our production! Get to know us better – visit our Site Hillerød career page: Career search results (novonordisk)

To find out more about our site go to: Novo Nordisk Hillerød

 
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 Novo Nordisk 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 Novo Nordisk, high business complexity and competing interests. We believe in personal development and have high ambitions for our collaborative performance.

Working at Novo Nordisk
At Novo Nordisk, 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, Director, AP Filling & Inspection, Peter Nøhr at +45 30799570 or penqnovonordisk

Deadline
16 October 2024.

Please upload your CV in English. 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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