Job Title: Quality Control Specialist IV – Microbial Control
Location: Portsmouth, NH, (On-site)
As a QC Specialist IV in Microbial Control at our Portsmouth site, you will support efforts to reduce contamination risk and maintain a high level of environmental control across manufacturing areas. You will focus on environmental monitoring, trending, and data analysis while supporting contamination control improvements and new equipment integration. This is a hands-on, collaborative role where you will work closely with manufacturing and quality teams to ensure compliance with cGMP standards.
This role follows a Monday through Friday schedule from 8:00 AM to 5:00 PM.
What you will get
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Medical, dental, and vision insurance
- Opportunities to grow and develop your career
- A collaborative and cross-functional work environment
- Perform environmental monitoring activities and ensure compliance with site standards
- Analyze environmental monitoring data and support routine trending activities
- Assess environmental impact and identify potential contamination risks
- Support investigations and root cause analysis related to contamination events and trends
- Assist with implementing contamination control improvements across the site
- Support integration and qualification of new equipment related to microbial control
- Partner with cross-functional teams to identify improvement opportunities and enhance processes
- Bachelor’s degree in a science-related field required
- Minimum of 3+ years of experience in microbiology or GMP manufacturing environments
- Experience with environmental monitoring, trending, and data analysis
- Understanding of contamination control principles and aseptic practices
- Experience supporting investigations and identifying trends in data
- Strong communication skills, with the ability to explain findings clearly
- Ability to work independently and collaborate across teams
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Reference: R77188
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About the company
Company website•Pharmaceutical Manufacturing
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.