Manufacturing Associate, III
On-sitePortsmouth, New Hampshire, United States
Job Summary
Set up, operate, and monitor manufacturing equipment, including CIP and SIP processes, while executing production tasks under cGMP and GDP requirements. Perform advanced laboratory tasks like sampling and pH testing, troubleshoot equipment issues, and review batch records to support deviation initiation. Train associates on manufacturing processes and maintain equipment through cleaning and sanitization. This role requires 3+ years of upstream bioprocessing experience and follows a 12-hour rotating day shift from 7:00 AM to 7:00 PM. You will lead by example within a collaborative team focused on continuous improvement initiatives at Lonza's Portsmouth site.
Required Qualifications
- 3+ years of upstream bioprocessing experience
- High school diploma or equivalent
- Ability to troubleshoot equipment and support investigations
- Strong communication skills, including technical writing
- Attention to detail with strong problem-solving and decision-making skills
Desired Qualifications
- 5+ years in the biotech industry
- Experience in GMP manufacturing or a regulated biopharmaceutical environment
- Strong understanding of cGMP, documentation practices, and process flow
- Associate's or Bachelor's degree in a science-related field
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.