Lonza America Inc

Project Engineer 3

Lonza America Inc$95K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering (preferably Chemical, Mechanical, or Biopharmaceutical)
  • 5-10 years of experience in pharmaceutical/biotechnology sectors
  • Proficiency in the design and operation of biopharmaceutical facilities
  • Familiarity with control systems (PLC, DCS, Loop controllers)
  • Demonstrated project management experience in industrial settings
  • Proven ability to coordinate with engineering and construction teams
  • Strong grasp of design principles and standards in biopharmaceutical facilities

Responsibilities

  • Lead root cause analyses and optimize preventative maintenance plans
  • Plan and execute capital plant projects, managing contractors and commissioning protocols
  • Act as the lead technical owner for P&IDs and technology transfers
  • Handle change requests and lead quality risk assessments
  • Revise SOPs and validation protocols, updating essential engineering documents
  • Serve as engineering Subject Matter Expert during facility audits
  • Demonstrate safety leadership while managing project timelines

Benefits

  • Relocation assistance for eligible candidates and families
  • Comprehensive access to global benefits and career resources
  • Support for professional development and continued education
  • Work in a dynamic, on-site environment that fosters innovation
  • Engagement in projects that shape the future of life sciences
Full Job Description
Project Engineer 3

Location: On-site, Portsmouth, NH. Relocation assistance is available for eligible candidates and their families.

The Plant Engineer 3 role supports ongoing Lonza operations by providing technical leadership as it relates to manufacturing and process systems. The role acts as a technical resource to operations customers to ensure that equipment and facilities are designed, operated, and maintained to meet production needs. Responsibilities of the role include implementation of engineering projects to support manufacturing requirements.

What you will do:
  • Equipment Reliability & Maintenance: Lead root cause analysis, resolve major equipment breakdowns, and sustain maintenance programs by optimizing preventative maintenance plans.
  • Project & Contractor Management: Plan and execute capital plant projects, oversee commissioning protocols, and manage engineering contractors.
  • Process Engineering & Tech Transfer: Serve as the technical owner of P&IDs and process equipment, acting as the lead for new technology transfers.
  • Quality & Compliance Support: Own change requests and CAPA actions, assist with deviation investigations, and lead quality risk assessments.
  • Documentation & Asset Review: Review and revise SOPs, batch records, and validation protocols, while updating critical engineering documents and drawings.
  • Audit Subject Matter Expert: Act as the engineering Subject Matter Expert (SME) during facility audits and inspections.
  • Safety & Execution: Demonstrate safety leadership by example and balance priorities effectively to meet project milestones and timelines.


What we are looking for:
  • Bachelor's degree is required. Engineering (Chemical, Mechanical, Biopharmaceutical are referred areas of study) discipline with 5-10 years of substantial pharmaceutical/biotechnology experience (or equivalent).
  • Experience in the design and operation of Biopharmaceutical facilities, both manufacturing and support systems.
  • Experience with control systems (PLC, DCS, Loop controllers) desirable.
  • Project management and coordination experience associated with the execution of capital projects in an industrial environment in required.
  • Practical experience in the management and coordination of engineering and construction management consultants, equipment vendors and contractors is required.
  • Ability to handle multiple projects simultaneously, keeping track of costs and schedule and ensuring compliance with quality and safety standards.
  • A solid understanding of design principles and standards within Biopharmaceutical facilities.


Access to our full list of global benefits: https://www.lonza.com/careers/benefits

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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