Director for Inspection Office
at Novo Nordisk
Bagsværd, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 20 Nov, 2024 | Not Specified | 17 Nov, 2024 | N/A | Ema,Business Acumen,Management Skills,Presentation Skills,English,Knowledge Sharing,Gmp,Iso,Danish | No | No |
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Description:
Director for Inspection Office
Category: Quality
Location:Bagsværd, Capital Region of Denmark, DK
Do you want to grow your potential at an expert level in a truly international environment? Do you have profound GMP compliance experience and a proven track record from GMP inspections? If this sounds interesting, you might very well be our new Director – so seize this excellent opportunity for the next step in your life-changing career!
QUALIFICATIONS
To be successful in this role, you should have:
- Extensive experience within quality and GMP at a specialist/leader level.
- GMP inspection experience, including DKMA, EMA and FDA interaction.
- Knowledge within medical device inspections and ISO 13485 is advantageous.
- Strong ability to work with diverse cross-functional colleagues.
- Excellent interpersonal and stakeholder management skills, with a preference for international work experience, business acumen, solid presentation skills, and the willingness and ability to lead during change, take initiative, be agile in actions, and embrace new ways of working.
- Fluency in written and spoken English, written and spoken Danish is advantageous.
As a person, you are open and communicative, with the ability to reach out and engage with multiple stakeholders. Your positive attitude and proactive can-do behaviour energise your colleagues and stakeholders, ensuring engagement and commitment wherever you go. You enjoy knowledge sharing, and your quality mindset and solution focus is a natural part of you. The structure you are applying to tasks helps you prioritise even when things are moving fast. You appreciate the value of accurate and timely documentation as the essential safety and quality control parameter.
Responsibilities:
- Extensive experience within quality and GMP at a specialist/leader level.
- GMP inspection experience, including DKMA, EMA and FDA interaction.
- Knowledge within medical device inspections and ISO 13485 is advantageous.
- Strong ability to work with diverse cross-functional colleagues.
- Excellent interpersonal and stakeholder management skills, with a preference for international work experience, business acumen, solid presentation skills, and the willingness and ability to lead during change, take initiative, be agile in actions, and embrace new ways of working.
- Fluency in written and spoken English, written and spoken Danish is advantageous
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Bagsværd, Denmark