What are the responsibilities and job description for the Sr. Validation Engineer, Process Validation position at EPM Scientific?
Join a Leading CDMO in the Midwest!
Are you a skilled professional with expertise in drug product manufacturing and process validation? Our client, a leading organization in the CDMO sector, is seeking a talented Senior Process Validation Engineer to become a cornerstone of their operations team. Located in the Midwest, this permanent role offers you the opportunity to join a dynamic environment where innovation meets excellence. You'll work with cutting-edge technology and contribute to delivering high-quality biotech solutions.
- Drug Product Manufacturing Expertise: Deep knowledge and hands-on experience in drug product manufacturing processes.
- Process Validation Skills: Proven ability in designing and executing validation protocols to ensure robust and compliant processes.
- Collaborative Mindset: Willingness to work closely with cross-functional teams to enhance operational effectiveness.
Be part of an organization that values innovation, precision, and dedication to delivering industry-leading solutions. This role will provide you with opportunities to work on impactful projects in a supportive and expert environment.
If you're ready to take your career to the next level and make a meaningful impact in the CDMO industry, apply today! Don't miss this chance to advance within a sector that's shaping the future of biotech.
