QC Analyst I-Microbial Control

Lonza Group; Portsmouth (NH); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Overnight shift differential

Career growth and development

Hands-on training

Team-focused laboratory environment

Job summary

Lonza Group in Portsmouth, NH is seeking a Quality Control Analyst I – Microbial Control to support microbiological testing and monitoring. This on-site role involves lab testing, environmental monitoring, and meticulous documentation under cGMP.

You’ll work overnight Wednesday through Saturday, with shift differentials for nights and weekends, and participate in hands-on training within a collaborative laboratory team.

Qualifications

• Associate degree in microbiology, biochemistry or related field required or preferred.
• Experience in a regulated lab environment desirable.
• Strong attention to detail and ability to follow procedures.

Responsibilities

• Perform microbiological testing for in-process, release, and stability samples under guidance.
• Support environmental and utility monitoring, including HVAC and facility sampling.
• Record and document test results following GMP and data integrity standards.
• Use laboratory systems and basic software to enter and manage data.
• Assist in identifying deviations and escalate issues to senior team members.
• Follow cGMP, GDP, and data integrity requirements in all tasks.
• Participate in routine lab activities, including sample handling and cleaning.

Skills

Microbiology knowledge

Attention to detail

Documentation skills

Teamwork

Communication skills

Education

Associate’s degree in Microbiology, Biochemistry, or related science

Tools

Laboratory information systems

GMP data entry

Job description

United States, Portsmouth (New Hampshire)

Job Title: Quality Control Analyst I – Microbial Control

Location: Portsmouth, NH, (On-site)

As a QC Analyst I in Microbial Control at our Portsmouth site, you will support microbiological testing and monitoring activities to help ensure the safety and quality of drug products. You will assist with laboratory testing, environmental monitoring, and documentation while working under the guidance of experienced team members. This role is based onsite, where hands-on laboratory work and collaboration are essential to maintaining quality and compliance with cGMP standards.

The position follows a Wednesday throughSaturday schedule, working overnight from 8:30 PM to 7:00 AM . Shift differentials are offered for Nights and Weekends worked.

What you will get

• Competitive pay and performance-based compensation
• Medical, dental, and vision insurance
• A supportive and inclusive work environment
• Opportunities for career growth and development
• Hands-on training and skill-building
• A collaborative and team-focused laboratory environment

What you will do

• Perform microbiological testing for in-process, release, and stability samples with guidance
• Support environmental and utility monitoring, including HVAC and facility sampling
• Record and document test results following GMP and data integrity standards
• Use laboratory systems and basic software to enter and manage data
• Assist in identifying deviations and elevate issues to senior team members
• Follow cGMP, GDP, and data integrity requirements in all assigned tasks
• Participate in routine lab activities, including sample handling and cleaning

What we are looking for

• Associate’s degree in Microbiology, Biochemistry, or a related science field
• Limited experience in a laboratory or regulated environment preferred
• Basic understanding of laboratory techniques and aseptic practices preferred
• Strong attention to detail and ability to follow instructions
• Good written and verbal communication skills
• Ability to prioritize tasks and work as part of a team
• Comfortable working in cleanroom environments, including performing physical tasks such as climbing ladders when needed

About Lonza

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.