Senior Biotechnologist (Nights - B Shift)

Lonza • Portsmouth, NH

287d

About The Position

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of! What sets this opportunity apart is our dedication to encouraging an environment where innovation thrives. At Lonza AG, you'll work alongside dedicated colleagues, contributing to our brand new manufacturing processes in New Hampshire, USA. As a Senior Biotechnologist, you will have a meaningful role in our ambitious goals to develop and produce innovative biotechnological products. This position is for the night shift from 7pm-7am, on a rotational schedule every other week: Week 1: M/T - F/SAT/SUN Week 2: W/TH Shift differentials are included for nights and weekends worked.

Requirements

• A minimum of a High School Diploma or equivalent experience; an AS/BS in a science-related field is preferred.
• Extensive experience in the biopharmaceutical manufacturing industry, demonstrating proven logic, decision-making abilities, and critical thinking skills.
• Outstanding written and verbal communication skills are essential.
• Demonstrates flexibility in adapting to changing business priorities and actively seeks feedback for continuous improvement.

Responsibilities

• Successfully implement and optimize biotechnological manufacturing processes, ensuring flawless execution and adherence to cGMP conditions.
• Strictly monitor and operate bioprocessing equipment, maintaining the highest standards of performance and safety.
• Independently perform laboratory tasks, including pH and conductivity testing, product sampling, and routine sanitization to maintain both facility and equipment integrity.
• Train and mentor other technicians, encouraging a collaborative and inclusive work environment while ensuring they are proficient in cGMP compliance and technical procedures.
• Review and assess batch records and logbooks for accuracy, clarity, and completeness, submitting necessary revisions to maintain documentation excellence.
• Tackle complex and non-routine equipment issues, initiating deviations and providing detailed analysis to determine root causes and corrective actions.
• Lead administrative tasks such as shift exchanges, team meetings, and project participation, ensuring smooth and efficient operations.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: High school or GED