QC Analyst I-Microbial Control

Lonza; Portsmouth (NH); On-site; Confidential; Full time

Benefits offered by this job

Competitive pay

Medical Insurance

Inclusive culture

Career growth

Hands-on training

Collaborative lab

Job summary

Lonza in Portsmouth, NH is seeking a Quality Control Analyst I for Microbial Control to support microbiological testing and monitoring activities. This on-site role involves hands-on laboratory work under guidance, with a Wednesday–Saturday overnight schedule (8:30 PM–7:00 AM) and shift differentials for nights/weekends.

You will help ensure drug product safety and quality in a cGMP environment. The position emphasizes data integrity, GMP compliance, and collaboration within a team, offering

Qualifications

• 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

Responsibilities

• 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

Skills

Microbiology

Biochemistry

Lab techniques

Attention to detail

Communication

Education

Associate’s degree in Microbiology

Tools

GMP systems

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 through Saturday 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.

Ready to shape the future of life sciences? Apply now.