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Specialist, Production GMP Support
4 months ago
Excited about quality, compliance, and continuous improvements?
If you have a solid understanding and experience with GMP requirements in pharmaceutical production, we want you as our next experienced GMP Specialist.
Your New Role - Why Choose Us?
You'll have a dynamic, independent job with a lot of influence where you'll support Lundbeck Pharmaceutical production, drive root cause analysis, and lead GMP projects. Embrace challenges with a structured approach and collaborate closely with colleagues to identify improvement opportunities.
- Provide primary GMP support to production.
- Take part in complex projects, guiding stakeholders in the right direction.
- Ensure high quality and compliance through a continuous improvement mindset.
- Review and approve quality-related documents.
- Participate in inspections and audits.
Your Future Team
Join the Production GMP Support team with 11 dedicated members supporting Solid Bulk Production and Finished Goods Production. Work within Lundbeck's headquarter in Valby, part of the Pharmaceutical Production & Supply Chain.
Your Contribution
- Degree in pharmaceutical science or relevant field.
- Practical experience in GxP.
- Advanced continuous improvement experience.
- Ability to thrive in a fast-paced environment and collaborate effectively.
- Strong communication skills in Danish and English.
Show positivity, flexibility, and persistence. Enjoy a dynamic work setting, being a proactive team player with a can-do attitude.
Our Commitment to You
Experience a collaborative culture at Lundbeck offering exciting tasks, growth opportunities, and well-being initiatives. Your career growth and progress are important to us as we work towards improving brain health for all.
Interested? Join Us
If this role resonates with you, share your motivation and apply by 10th June 2024. We value diversity and the unique perspectives each individual brings. Learn more about our commitment and stay connected with us.
