Lonza America Inc

Senior Production Support, Biotechnologist

Lonza America Inc$80K — $110K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience in cGMP biological manufacturing or regulated clinical lab environment required.
  • Solid understanding of aseptic techniques, hygienic processing, and basic microbiology principles.
  • Proficient in proactive communication and superior organizational skills for cross-department coordination.
  • Ability to adapt to dynamic, shifting priorities in a pharmaceutical manufacturing environment.
  • High School Diploma required; Bachelor's Degree in life sciences preferred.
  • Must be able to follow cleanroom protocols and lift up to 50 lbs.

Responsibilities

  • Lead technical coordination and staging of process-critical materials and equipment to eliminate production delays.
  • Facilitate management of reusable parts, including parts cleaning and sterilization processes.
  • Support media and buffer production by weighing and dispensing materials as per specifications.
  • Develop and execute suite readiness checklists to ensure manufacturing teams are prepared for campaigns.
  • Collaborate with supply chain and materials specialists to track inventory and monitor deliveries rhythmically.
  • Provide operational support during tech transfer phases, including facility water and particle runs.
  • Author and review GMP documentation to ensure compliance with regulations and standards.
  • Maintain processing proficiency to assist manufacturing teams directly on the floor when needed.
  • Ensure compliance with site safety objectives and cGMP guidelines during daily operations.

Benefits

  • Dynamic working culture with opportunities for agile career advancement.
  • Inclusive workplace committed to ethical practices.
  • Recognition programs in place for high performance.
  • Medical, dental, and vision insurance offered, alongside PTO and other benefits.
Full Job Description

Senior Production Support, Biotechnologist – 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

  • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you’ll do:

  • 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: 5+ years of experience within a cGMP biological manufacturing or regulated clinical laboratory environment is required.

  • 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.

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

About Lonza America Inc

Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
Learn more about Lonza America Inc
Size
16,218 employees
Industry
NASDAQ

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