GMP Coordinator for QC

Job title:

GMP Coordinator for QC

Company:

Novo Nordisk

Job description

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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:GMP Coordinator for QCCategory: QualityLocation:Hillerød, Capital Region of Denmark, DKDo you have a combination of QA knowledge and understanding of a GMP-regulated laboratory environment? Would you like to set the direction for the department’s quality level?If so, you might be our new colleague! Apply today for a life-changing careers and join us as a GMP Coordinator in Aseptic Manufacturing Science and Technology.The position
As a GMP Coordinator, you become the department’s Quality Manager and together with other GMP Coordinators in AMSAT QC, you will have the opportunity to work with many exciting tasks across the VP area.In this role, you will be responsible for supporting the department in developing and maintaining a high cGMP level.Your key responsibilities will be:

• Supporting the department to maintain a high level of compliance with cGMP and Novo Nordisk Quality Management System.
• Supporting continuous improvements of quality performance and processes by participating in department target setting, identifying continuous improvement opportunities and proposing actions to take.
• Driving and improving processes that create transparency for key quality indicating parameters (Quality Oversight) for example by collecting inputs, preparing and following up on Quality Management Review, and deviation and QMTs.
• Identifying trends and propose areas where actions should be taken.
• Acting as one-point of contact for GMP partners and local responsible for coordination of Inspections and Audits.

Your job will be characterized by a dynamic mix of coordination, follow-up and execution of your own tasks in a focused manner, so you must be able to, and be motivated by, a flexible workstyle and ability to prioritize your own tasks and time.Qualifications
You will be part of a team in a dynamic and complex environment, where flexibility and the ability to prioritize are an advantage.To qualify for the position, we imagine that you have:

• MSc/BSc within Pharmacy, Chemical Engineering, Chemistry/Biology or similar.
• Preferably 2 or more years’ experience from the pharmaceutical or medical device industry or similar related areas.
• Solid experience with authority inspections and audits.
• Proven strong skills within GMP and coordination.
• Experience or knowledge in project management, Lean and/or data systems (Tableau, or similar) would be an advantage.

On a personal level, you are curious, resourceful, and independent. You want to develop yourself personally, and you enjoy working closely with people from different educational backgrounds. In the team, we value commitment, openness, and a positive attitude.About the Department
In Aseptic Manufacturing, Science and Technology (AMSAT) QC Hillerød, our core task is analyzing some of Novo’s newest products. The department currently provides analysis results used in connection with the release of both marketed and new products, stability studies, and development experiments. In addition, we have a strong focus on digitization and automation.”The department consists of approximately 60 employees divided into 5 teams. You will be part of the department’s support team, which consists of 3 LIMS static builders, project manager, innovation scientists, planning coordinator. The support team works the department to support the 4 operational teams.Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.Contact
If you have any questions, feel free to contact Manager Britt Aaboe Jørgensen at +4530755549.Deadline
30 December 2024You 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.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.

Expected salary

Location

Hillerød, Hovedstaden

Job date

Wed, 11 Dec 2024 06:23:20 GMT

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