Biotechnologist I — Night Shift, GMP Downstream

Lonza Biologics, Inc.; Portsmouth (VA); On-site; Confidential; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Competitive compensation programs

Medical, dental, and vision insurance

Career growth opportunities

Collaborative team environment

Job summary

Lonza Biologics, Inc. in Portsmouth, NH, is seeking a Biotechnologist I to support production of therapeutic proteins in a GMP setting. You will operate equipment, perform downstream purification, and assist in safe, high-quality manufacturing.

The role includes shift work on a 12-hour cycle with two on/off patterns. Ideal candidates have a science background and hands-on biopharma experience, with strong attention to detail and teamwork.

Qualifications

• High school diploma or equivalent required; AS/BS preferred.
• Experience in biopharmaceutical manufacturing or regulated production preferred.
• Experience with downstream purification processes or chromatography preferred.

Responsibilities

• Set up, operate, and monitor manufacturing equipment including purification systems.
• Execute downstream manufacturing operations such as chromatography and filtration.
• Support column packing and viral reduction filtration activities.
• Perform laboratory tasks like pH testing and product sampling.
• Move and transfer materials across production areas safely and accurately.
• Maintain equipment and facilities through routine cleaning and sanitization.
• Troubleshoot basic equipment issues and assist with documentation reviews.
• Participate in shift handovers and team improvement initiatives.

Skills

Hands-on bioscience

Problem solving

Teamwork

Attention to detail

Education

High school diploma or equivalent

AS/BS in a science-related field preferred

Tools

Microsoft Office

Job description

Lonza Biologics, Inc. in Portsmouth, NH, is seeking a Biotechnologist I to support production of therapeutic proteins in a GMP setting. You will operate equipment, perform downstream purification, and assist in safe, high-quality manufacturing.

The role includes shift work on a 12-hour cycle with two on/off patterns. Ideal candidates have a science background and hands-on biopharma experience, with strong attention to detail and teamwork.