QA Specialist III-Operations

QA Specialist III-Operations

Lonza – Onsite in Portsmouth, NH, United States (New Hampshire). This role focuses on reviewing and approving GMP documentation to support operations and ensure compliance.

• 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

• 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

• 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

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.

Reference: R71865

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