Production Support, Biotechnologist II

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

Benefits offered by this job

Agile culture

Inclusive workplace

Compensation programs

Medical, dental and vision insurance

PTO

Job summary

Lonza in Portsmouth, NH, is seeking a Production Support Biotechnologist II to ensure flawless material flow and readiness of manufacturing suites for large-scale allogenic bioprocessing. You will coordinate staging of single-use bioreactors, consumables, and raw materials, while supporting BOM management, procurement tracking, and tech transfer milestones.

Strong communication, aseptic techniques, and cleanroom experience are essential.

Qualifications

• 1–3 years of experience in cGMP biomanufacturing or regulated labs.
• Hands-on cleanroom experience highly preferred.
• Strong understanding of aseptic techniques and hygienic processing.

Responsibilities

• Lead material staging of process-critical materials, consumables, and equipment to prevent floor delays.
• Manage reusable parts, including parts washer and autoclave where applicable.
• Weigh and dispense components for media and buffers.
• Ensure suite readiness and on-time delivery for campaigns.
• Track procurement requests and monitor BOM inventories.

Skills

Proactive communication

Computer literacy

Organizational skills

Aseptic techniques

Education

High School Diploma or equivalent

Bachelor’s Degree in Life Sciences

Tools

Microsoft Office

Job description

United States, Portsmouth (New Hampshire)

Production Support, Biotechnologist II – Large Scale Allogenic Manufacturing

Location: Portsmouth, NH, USA.

Schedule: Monday – Friday, 8:00 AM – 5:00 PM (Standard Business Hours). Note: Flexibility to adjust schedules to support shifting campaign timelines or floor demands may be required.

We are seeking a proactive and highly organized technical professional to join our team in Portsmouth, NH, as a Production Support Biotechnologist II. This specialized role is designed for a candidate with a traditional cGMP biomanufacturing background who wants to focus on the operational staging, material lifecycle management, and equipment readiness that makes production possible. Operating under general supervision, you will ensure that the production suites have a flawless, continuous supply of materials—including single-use bioreactors, specialized raw materials, and processing consumables. While your primary mandate is logistical readiness and material flow, you will maintain the technical baseline necessary to jump onto the manufacturing floor and support production operations directly when campaigns reach full-scale execution.

What will you get?

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• Medical, dental and vision insurance, as well as PTO and more

Material & Equipment Staging: Lead the technical coordination, staging, and movement of all process-critical materials, consumables, and equipment (including single-use bioreactor assemblies and hardware) to prevent floor delays.

Re-usable Parts Management: Facilitate management of reusable parts include use of the parts washer and autoclave where applicable.

Weigh & Dispense: Support production of media and buffers by weighing components to be used in media/buffer formulation.

Suite Readiness & On-Time Delivery: Support the development and execution of robust suite readiness checklists, ensuring manufacturing teams are fully set up for flawless campaign execution.

Cross-Functional Procurement Tracking: Partner with internal supply chain and materials specialists to track purchase requisitions, manage BOM inventories, and monitor deliveries against strict project metrics.

Technical Transfer Operational Support: Provide crucial operational and material-flow support during tech transfer milestones, including facility water runs, particle runs, and engineering runs.

Documentation Compliance: Author, review, and execute GMP documentation—including Standard Operating Procedures (SOPs), Work Instructions (WIs), and material tracking sheets—ensuring total GDP compliance.

Direct Manufacturing Assistance: Maintain processing proficiency across core unit operations (e.g., cell growth, harvest, or fill/finish) to seamlessly jump in and directly assist manufacturing teams on the floor as production demand dictates.

Quality & EHS Alignment: Manage daily tasks in strict compliance with site safety objectives and cGMP guidelines, actively participating in room clearance, facility sanitization, and the resolution of material-related deviations.

What we’re looking for:

Experience: 1–3 years of experience within a cGMP biological manufacturing or regulated clinical laboratory environment is required. Prior hands-on experience inside a cleanroom setting is highly preferred.

Technical Background: Background identical to a standard manufacturing associate, including an understanding of aseptic techniques, hygienic processing concepts, and basic microbiology principles.

Skills: Excellent proactive communication, strong computer literacy, and superior organizational skills required to coordinate complex material requirements across multiple internal departments.

Adaptability: Ability to think quickly, draw accurate conclusions, and thrive under the dynamic, shifting priorities of an active pharmaceutical manufacturing asset.

Education: High School Diploma or equivalent is required. A Bachelor’s Degree in a life sciences discipline (Biology, Biotechnology, Biochemistry, etc.) is strongly preferred.

Physical Requirements: Ability to sit, stand, walk the production floor for extended periods, comfortably handle continuous cleanroom gowning protocols, and occasionally lift up to 50 lbs.

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.