Validation and Compliance Specialist
at Novo Nordisk
Kongens Lyngby, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Nov, 2024 | Not Specified | 20 Oct, 2024 | 1 year(s) or above | Validation,Technical Requirements,It,International Travel,Iso,Collaboration,Supply Chain Operations | No | No |
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Description:
Validation and Compliance Specialist
Category: Project Management & Agile
Location:Lyngby, Capital Region of Denmark, DK
Are you driven to use your knowledge and experience to help others succeed? Are you ready for a work life where focus is on quality and delivery of life-saving medicines to our patients within intralogistics at our global future Fill & Finish sites?
If yes, then you might be the Validation and Compliance Specialist we are looking for. Apply for this exciting job opportunity at Novo Nordisk!
THE POSITION
Novo Nordisk is investing massively in new production facilities around the globe. With this expansion we will contribute with the important role of producing future products - and you will get an opportunity to be a part of it.
We are seeking a highly skilled and detail-oriented Validation and Compliance Specialist to join our intralogistics team. The ideal candidate will play a critical role in ensuring the validation and compliance of our intralogistics systems, adhering to industry standards and regulations. This individual will work closely with cross-functional teams to develop and execute validation strategies, while also maintaining compliance with relevant guidelines and requirements.
In this role, you will have the following responsibilities:
Develop and implement validation protocols and procedures for intralogistics systems, including material handling equipment, warehouse management systems, and automated storage solutions.
Conduct risk assessments and validation activities in accordance with regulatory requirements.
Collaborate with engineering and operations teams to perform validation testing, analyze results, and address any non-conformities or discrepancies.
Ensure compliance with safety, quality, and environmental standards, while also participating in continuous improvement initiatives to enhance intralogistics processes.QUALIFICATIONS
To be successful in this role, we are looking for a candidate with the following qualifications:
Bachelor’s degree in engineering, supply chain management, or a related field. A master’s degree is preferred.
Proven experience in validation and compliance within intralogistics, logistics, or supply chain operations.
Strong understanding of industry regulations and standards, such as FDA regulations, GAMP guidelines, and ISO 9001.
Excellent analytical and problem-solving skills, with the ability to interpret technical requirements and apply them to validation processes.
Exceptional communication and collaboration abilities, with a keen attention to detail and a commitment to delivering high-quality results.
As a person you are responsible and able to execute necessary decisions to solve the challenges with flair for efficiency and quality. It is important that you thrive in a challenging, dynamic, and changeable environment and no tasks is too big or too small to solve.
Your workplace will be based Lyngby but as there is collaboration required on a global scale with our sites based in Europe, China, and US, some international travel will be required. It is estimated this will be a few days per month. Sometimes you may be travelling for prolonged 1-2 weeks periods.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Logistics/Procurement
Pharma / Biotech / Healthcare / Medical / R&D
Logistics
Graduate
Management or a related field
Proficient
1
Kongens Lyngby, Denmark