QMS Professional- Project Management
at Novo Nordisk
Måløv, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Dec, 2024 | Not Specified | 25 Sep, 2024 | N/A | Management Skills,English,Communication Skills,Pharmaceutical Industry,Biopharmaceutics,Chemistry,Independence,Biology | No | No |
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Description:
QMS Professional- Project Management
Category: Quality
Location:Måløv, Capital Region of Denmark, DK
Are you a dedicated QMS professional looking to make a difference in the production of life-changing diabetes treatments? Do you have a passion for quality management systems and a desire to work in a diverse and inclusive workplace? If so, join our team in Emerging Technologies (ET) at Novo Nordisk!
QUALIFICATIONS
To succeed in this role, you should possess the following qualifications:
- An academic degree, preferably in Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics, or related fields.
- Relevant work experience in the medical device or pharmaceutical industry within QMS, Quality Assurance, production, or similar roles.
- Proven experience in driving or participating in projects and process improvement initiatives.
Fluency in written and spoken English; Danish language skills are an advantage.A strong quality-oriented, proactive, pragmatic mindset, with the ability to thrive in fast-paced environments. Strong stakeholder management skills are also essential.
On a personal level, you are ambitious, curious, proactive and have a strong interest in developing yourself and people in your network. You demonstrate a service-minded attitude, independence, a focus on simplicity and a sense of responsibility for your tasks. Finally, you exhibit excellent communication skills, enabling effective collaboration with individuals from diverse nationalities and cultures.
ABOUT THE DEPARTMENT
ET is anchored in Product Supply, which globally address 47,000 of Novo Nordisk’s 63,000 employees. In ET, we are approximately 2500 dedicated employees based primarily in Måløv (DK), but also in Durham (US) - and our sites are still growing. For the future we have many ambitions, and we are working hard to get our new tablet product on the market. Together we will succeed and still strive being at the forefront of the development of technology, systems, and processes etc.
You will join the QMS Team, part of the “Sustainable & Operational Excellence” department based in Taastrup. In the QMS Team, it is our main responsibility to deliver support of highest possible quality to the organization and to maintain/develop ET’s Quality Management System by ensuring efficiency and applicability in our QMS processes. We work together across the team and with colleagues across ET to continuously develop and improve our standards to provide aligned and effective tools that support a stable and compliant production.
In ET, we make a huge effort for you as a new employee to be off to a good start. During the first few days you will spend some time with other new employees, where you will go through an exciting introduction plan together. We know how important it is, and we are looking forward to meeting you.
Responsibilities:
As a Quality Management System (QMS) Professional, you will play a crucial role in driving quality initiatives and projects that will maintain and optimize our high standards of operation. Your responsibilities will include:
- Leading and implementing GMP projects across ET to improve processes and enhance project management skills.
- Guiding the maintenance, updates, and improvements of the current ET Quality Management System (QMS) processes while ensuring compliance with internal and external requirements.
- Promoting simplicity and cross-site harmonization across ET, Product Supply (PS), and other relevant areas within Novo Nordisk.
- Building and maintaining strong relationships with stakeholders across the ET organization and wider Novo Nordisk to set the strategic direction of QMS and other relevant initiatives
To succeed in this role, you should possess the following qualifications:
- An academic degree, preferably in Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics, or related fields.
- Relevant work experience in the medical device or pharmaceutical industry within QMS, Quality Assurance, production, or similar roles.
- Proven experience in driving or participating in projects and process improvement initiatives.
- Fluency in written and spoken English; Danish language skills are an advantage.A strong quality-oriented, proactive, pragmatic mindset, with the ability to thrive in fast-paced environments. Strong stakeholder management skills are also essential
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Engineering pharmacy chemistry biology biopharmaceutics or related fields
Proficient
1
Måløv, Denmark