Project Manager, Quality Assurance
at Lundbeck
København, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Sep, 2024 | Not Specified | 29 Jun, 2024 | 5 year(s) or above | Management Skills,Manufacturing,Soft Skills,Working Experience,Pharmaceutical Industry | 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:
Are you an experienced Project Manager eager to apply your experience and drive in improving our quality and compliance processes? We are looking for an experienced Project Manager who can transform and structure the processes that we use to ensure compliance.
WHAT YOU BRING TO THE TEAM
For this role, we are looking for a dedicated colleague with the following skills and competencies:
- Relevant education, such as Master´s degree in Pharmacy or equivalent.
- +5 years of relevant working experience within QA or manufacturing in the Pharmaceutical Industry.
- Previous experience with leading projects that has shown significant impact.
- Solid communication and stakeholder management skills.
- Good analytical mindset.
- Solid experience in working with data to support diagnostic.
- Soft skills, negotiating, convincing, etc.
APPLY NOW
Can you see yourself in this role? We want to hear from you.
Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!
Upload your CV and include a few lines about your motivation and reasons for applying. No separate cover letter is needed, and we ask you not to include a photo or personal information that does not relate to your professional experience.
If you have questions, please feel free to contact Anne Bekker-Jensen, Vice President, at abej@lundbeck.com. Applications must be received by 28th July 2024.
We need every brain in the game – and that includes all brains and the different perspectives we all bring to the table. At Lundbeck, we embrace the uniqueness of each employee, and we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at www.lundbeck.com/global/about-us/our-commitment/diversity-and-inclusion.
You can also learn more about us at www.lundbeck.com or by following us on LinkedIn, Instagram (@h_lundbeck) or Twitter (@Lundbeck).
Please feel free to share this opportunity with friends or those in your network who might find it interesting.
EveryBrainInTheGame
This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.
Responsibilities:
YOUR NEW ROLE
In this job, you will have an important role in securing compliance across our supply chain.
You will work closely with a broad range of stakeholders to support line of business in achieving compliance. You will use your project manager skills to improve current processes and to leverage the quality mindset across our organization. You will make sure that there is alignment and excellence in all steps from Data quality to reporting and escalation. The role is a unique opportunity to influence and continuously improve core quality systems and the decisions around quality.
In this position you will work across the organization and across sites in Lundbeck.
CPQS has a wide range of responsibilities amongst others:
- Continuous development of the global quality system
- Optimization of our business and quality processes
- Evaluation of new initiatives in the industry
- Internal and external audits
- Supplier evaluations
- GMP/GDP trainin
For this role, we are looking for a dedicated colleague with the following skills and competencies:
- Relevant education, such as Master´s degree in Pharmacy or equivalent.
- +5 years of relevant working experience within QA or manufacturing in the Pharmaceutical Industry.
- Previous experience with leading projects that has shown significant impact.
- Solid communication and stakeholder management skills.
- Good analytical mindset.
- Solid experience in working with data to support diagnostic.
- Soft skills, negotiating, convincing, etc
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Information Technology/IT
IT Software - Other
Software Testing
Graduate
Proficient
1
København, Denmark