QA Specialist III-Operations
Lonza•Portsmouth, NH
7d•Onsite
About The Position
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. Join Lonza and help us shape the future of life sciences.
Requirements
- 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
Responsibilities
- 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
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
