Quality Control Supervisor - Electrophoresis
Lonza
Summary
We're seeking a QC Supervisor, Electrophoresis to join our Quality Control team in Portsmouth, NH. In this leadership role, you'll guide a high-performing team responsible for the testing and release of raw materials, in-process samples, and final drug product lots. Your expertise will help ensure the delivery of accurate, compliant results while fostering a culture of quality, safety, continuous improvement, and patient-focused excellence.
Job description
This role follows a Monday-Friday, 8:00am – 4:30PM schedule.
What you will do
- Lead and support a team of QC analysts to deliver testing activities safely, accurately, and on schedule
- Plan and coordinate laboratory testing to meet manufacturing and customer timelines
- Review and approve quality control documentation and laboratory records
- Drive continuous improvement initiatives that enhance quality, efficiency, and compliance
- Support regulatory inspections, customer audits, investigations, and CAPA activities
- Resolve technical, operational, and team-related challenges in a timely manner
- Monitor compliance with cGMP requirements, quality systems, and data integrity standards
What we are looking for
- Bachelor's degree in a science-related field
- Experience working within a cGMP-regulated pharmaceutical, biotechnology, or life sciences environment
- Experience leading or mentoring laboratory teams
- Knowledge of electrophoresis testing and quality control laboratory operations
- Experience with quality systems such as LIMS, TrackWise, DMS, or electronic laboratory systems
- Strong troubleshooting, data review, and problem-solving skills
- Excellent written and verbal communication skills
- Ability to manage multiple priorities and deliver results in a fast-paced environment
- Commitment to safety, quality, compliance, and continuous improvement
Requirements
- Bachelor's degree in a science-related field
- Experience working within a cGMP-regulated pharmaceutical, biotechnology, or life sciences environment
- Experience leading or mentoring laboratory teams
- Knowledge of electrophoresis testing and quality control laboratory operations
- Experience with quality systems such as LIMS, TrackWise, DMS, or electronic laboratory systems
- Strong troubleshooting, data review, and problem-solving skills
- Excellent written and verbal communication skills
- Ability to manage multiple priorities and deliver results in a fast-paced environment
- Commitment to safety, quality, compliance, and continuous improvement
Benefits
- Medical, Dental & Vision
- Career Development
- Leadership Growth
- Competitive Salary
- Comprehensive Benefits
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.