Advanced Quality Assurance Professional in Aseptic Production

at  Novo Nordisk

Hillerød, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate02 Feb, 2025Not Specified22 Jan, 2025N/AChemistry,Team Development,Pharmaceutical Industry,Biology,English,Communication SkillsNoNo
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Description:

Advanced Quality Assurance Professional in Aseptic Production
Category: Quality
Location:Hillerød, Capital Region of Denmark, DK
Are you passionate about quality assurance? Do you have several years of experience within the pharmaceutical industry? We are looking for an Advanced Quality Assurance Professional in Aseptic Production to join our team in Hillerød. If you are ready for an exciting and challenging role, read on and apply today for a life-changing career.

QUALIFICATIONS

We are looking for a candidate with the following qualifications:

  • A master’s degree within Pharmacy, Engineering, Biology, Chemistry, or a similar field.
  • Professional experience in the pharmaceutical industry.
  • Experience with aseptic production is highly advantageous.
  • Fluent communication skills in Danish and English.

On a personal level, you should be ambitious, curious, proactive, and have a strong interest in personal and team development. You should also demonstrate a service-minded attitude, the ability to set direction, and a focus on simplicity. Excellent communication skills are essential for effective collaboration with stakeholders and colleagues.
About the department
At AM QA in Hillerød AP, we are responsible for the quality assurance of Aseptic Production in Hillerød. The department has grown significantly in 2024 and currently comprises 60 dedicated and engaged employees. Our team consists of 12 committed colleagues who succeed together. We are one of four teams in the department, and there is strong collaboration between the teams, ensuring flexibility and the development of competencies. We offer you an exciting and challenging job with committed colleagues.

Responsibilities:

  • Handle cases related to production on the automated inspection lines and Environmental Monitoring for the newest technology isolator lines.
  • Review and approve documents from production, such as batch documentation, deviations, change requests, and SOP updates.
  • Engage in validation activities and participate in projects. Collaborate with the team to solve challenges through open and honest dialogue.
  • Contribute to the continuous improvement of our way of working and embrace new ideas.
  • Engage in dialogue with production regarding quality topics to ensure alignment and continuous improvement


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Pharmacy engineering biology chemistry or a similar field

Proficient

1

Hillerød, Denmark