Ambitious Validation QA professional at Novo Nordisk
Måløv, Region Hovedstaden, Denmark -
Full Time


Start Date

Immediate

Expiry Date

23 Apr, 25

Salary

0.0

Posted On

24 Jan, 25

Experience

2 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Pharmaceutical Industry, Chemical Engineering, Role Model, International Environment, English

Industry

Pharmaceuticals

Description

Ambitious Validation QA professional
Category: Quality
Location:Måløv, Capital Region of Denmark, DK
Are you an equipment or QA Professional, who is eager to set direction and to ensure compliance, in close work with your stakeholders? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle? Do you believe in working together is better than working on your own? Then keep reading.

QUALIFICATIONS

We seek a colleague who fits our team both professionally and personally. As a person you are open minded, have an outgoing attitude and have strong communication and collaboration skills with both your colleagues in QA and stakeholders.

Also:

  • You hold a Master’s degree in chemical engineering, pharmacy or other relevant MSc.
  • Preferably you have minimum 2 years of experience within the pharmaceutical industry and/or qualification experience.
  • You dare to challenge us in our way of working and have a desire to take initiative as well as responsibility for your own learning.
  • We operate both in a national and international environment, so you must speak and write Danish and English fluently.

As a person, you are a role model for behaviour, a dedicated team player who inspires trust and respect among colleagues and partners. You are open-minded, with a high-quality mindset, and work with a high level of energy, an outgoing attitude, and natural networking skills. These qualities combine to make you an individual who is poised to contribute effectively within a professional setting.

Responsibilities
  • Have an overview of what is happening in production and participate in relevant projects.
  • Approval of documentation, such as qualification, deviations, change control, SOP, trend reports etc.
  • Being a trustworthy partner with stakeholders and setting the quality direction.
  • Setting the necessary QA direction in various tasks
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