Manufacturing Project Specialist

Responsibilities

• Lead manufacturing readiness activities for production campaigns
• Review and approve manufacturing documents, including SOPs, batch records, and validation protocols
• Collaborate with teams to develop and improve manufacturing processes and procedures
• Identify risks and implement mitigation strategies to support successful execution
• Manage improvement projects from concept through completion
• Support document creation and accuracy using analysis, dry runs, and mock set-ups
• Represent Manufacturing in meetings and communicate progress, risks, and updates

Requirements

• Bachelor's degree in Biotechnology, Biology, Chemistry, or a related field
• 5-7 years of experience in biotechnology or a similar manufacturing environment
• Strong written and verbal communication skills, including technical writing
• Effective planning, time management, and organizational skills
• Strong attention to detail and problem-solving abilities
• Experience with SAP is an advantage
• Proficiency in Microsoft Office tools, including Word, Excel, and PowerPoint
• About Lonza
• Ready to shape the future of life sciences?

Additional Information

Manufacturing Project Specialist Location: Portsmouth, NH, USA Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. The Manufacturing Project Specialist is responsible for ensuring manufacturing readiness across production suites and support areas. You will lead planning, coordination, and execution activities to support safe, compliant, and efficient campaign delivery. Working cross-functionally, you will partner with internal teams, customers, and subject matter experts to ensure manufacturing is set up for success. What you will get Competitive salary and comprehensive benefits package Opportunities for career growth and ongoing development Exposure to cross-functional collaboration and project leadership A supportive, team-oriented work environment The opportunity to contribute to life-changing products and therapies A culture focused on safety, quality, and continuous improvement

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