Quality Assurance Specialist
2 weeks ago
Unlock Your Potential in CMC Development
Lundbeck is seeking a highly skilled Quality Assurance Specialist to join our CMC Development team. As a key member of our team, you will play a critical role in ensuring the quality and compliance of our Investigational Medicinal Products (IMPs) for clinical trials.
About the Role
You will be responsible for reviewing batch records, conducting QA assessments, and approving master batch records. Your attention to detail and analytical skills will be essential in identifying and resolving deviations, change controls, and laboratory deviations. Additionally, you will contribute to vendor oversight and handle complaints in a timely and professional manner.
What We Offer
As a Quality Assurance Specialist at Lundbeck, you will have the opportunity to work with a talented team of professionals who are passionate about delivering high-quality products. We offer a dynamic and collaborative work environment, with a focus on employee development and growth. You will have the chance to contribute to the development of our processes and procedures, and to make a meaningful impact on the success of our organization.
Requirements
- A master's degree in pharmacy, chemistry, biology, or a related field
- Minimum 2 years of experience in a GMP regulated environment, preferably in manufacturing, quality control, or quality assurance
- Knowledge and competencies within CMC are preferred
- Fluency in English is required
How to Apply
If you are a motivated and detail-oriented individual with a passion for quality assurance, we encourage you to apply for this exciting opportunity. Please upload your CV and include a few lines about your motivation for applying. We look forward to hearing from you
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