What are the responsibilities and job description for the QA Specialist III- Operations position at Lonza?
QA Specialist III-Operations
Onsite in Portsmouth, NH
Join Lonza and help us shape the future of life sciences. As a Quality Assurance Specialist III, you will play a key role in reviewing and approving GMP documentation to support our operations and ensure compliance.
What you will get:
Competitive salary and comprehensive benefits package
Opportunities for professional growth and development
Collaborative and inclusive work environment
Access to cutting-edge technologies and global projects
Support for work-life balance
Employee recognition programs
Health and wellness initiatives
What you will do:
Review and approve GMP documentation for site operations
Serve as QA Subject Matter Expert for equipment and validation documents
Ensure compliance with Lonza documentation standards and procedures
Collaborate with internal teams to resolve documentation issues
Participate in interdepartmental projects and routine meetings
Apply data integrity principles in all aspects of work
Provide training and mentorship to junior team members
What we are looking for:
Bachelor’s degree in a scientific field
5-10 years of experience in Quality Assurance and GMP environments
Strong understanding of GMP regulations and documentation processes
Excellent communication and collaboration skills
Ability to manage multiple priorities effectively
Proficiency in enterprise systems and Microsoft Office tools
Business fluent in English
About Lonza:
Lonza is a global leader in life sciences, dedicated to enabling a healthier world. Our work impacts millions of lives every day.
Lonza is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Ready to shape the future of life sciences? Apply now.