Environmental Monitoring Professional
at Novo Nordisk
Bagsværd, Region Hovedstaden, Denmark -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 27 Sep, 2024 | Not Specified | 20 Sep, 2024 | 2 year(s) or above | Project Planning,Danish,Change Requests,It,Training,Gmp,Collaboration,Clean Room Design,Environmental Monitoring,Operators,Pharmaceutical Industry,English,Cross Functional Communication,Communication Skills,Deviations,Documentation,Stakeholder Management | No | No |
Required Visa Status:
| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
| GC Green Card |
Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
Environmental Monitoring Professional
Category: Manufacturing
Location:Bagsværd, Capital Region of Denmark, DK
Are you a dedicated pharmacist, (micro)biologist or similar academic with an interest in environmental improvement of aseptic production? Do you want to be an active part of the development of one of our most important production facilities in Novo Nordisk?
If your answer is yes, apply today and join us for a life-changing career!
QUALIFICATIONS
To succeed in this role, you have:
- A master’s or PhD degree within natural science, pharmaceutical science, engineering and a minimum of 2 years of relevant experience in EM.
- Experience within GMP, environmental monitoring, Clean-room design in manufacturing (preferably aseptic) environments.
- Experience with isolator technology or digitalization of EM-related documentation would be an advantage.
- Experience with LEAN, optimisation and systematic troubleshooting is a plus.
- Previously worked with documentation, qualification, change requests and deviations within the pharmaceutical industry.
- Excellent communication skills in English and Danish.
As a person, you have a solution-oriented, structured mindset and make decisions based on data. You are good at analysing, identifying, and mitigating risks. You make realistic and reliable plans. Most of all, you are a master in the art of collaboration, but you are ready to take the lead on discovering and defining opportunities to drive our projects forward.
It is an advantage if you have experience with project management including cross-functional communication and stakeholder management, project planning, risk management and deliverable tracking.
Responsibilities:
The main tasks will be to:
- Work on projects to implement new EM requirements into our facility
To succeed in this role, you have:
- A master’s or PhD degree within natural science, pharmaceutical science, engineering and a minimum of 2 years of relevant experience in EM.
- Experience within GMP, environmental monitoring, Clean-room design in manufacturing (preferably aseptic) environments.
- Experience with isolator technology or digitalization of EM-related documentation would be an advantage.
- Experience with LEAN, optimisation and systematic troubleshooting is a plus.
- Previously worked with documentation, qualification, change requests and deviations within the pharmaceutical industry.
- Excellent communication skills in English and Danish
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Information Technology/IT
IT Software - Other
Software Engineering
Graduate
Em
Proficient
1
Bagsværd, Denmark
