Lonza America Inc

Senior Process Engineer - Viral Vector

Lonza America Inc$110K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemical, Mechanical, Industrial, Electrical or related fields.
  • 5-10 years of experience in Pharmaceutical or Biotechnology Manufacturing.
  • Strong troubleshooting, analytical, and problem-solving skills.
  • Deep understanding of GEP/cGMP/GDP principles related to maintenance and documentation.
  • Experience in developing URSs, technical specifications, and SOPs.
  • Excellent leadership skills and ability to work with minimal supervision.
  • Proficiency in spreadsheets, databases, and word processing software.

Responsibilities

  • Lead troubleshooting for equipment and process issues in manufacturing.
  • Collaborate with Reliability Engineers to enhance equipment reliability.
  • Provide engineering support for selecting new equipment based on process needs.
  • Monitor and drive continuous improvement initiatives across processes.
  • Conduct failure analysis and ensure implementation of corrective actions.
  • Manage change controls, deviations, and validation efforts.
  • Develop technical documentation to support validation and audit activities.

Benefits

  • Relocation assistance available for eligible candidates and their families.
  • Fully site-based role promoting real-time collaboration.
  • Opportunity to work in a high-quality and safety-conscious manufacturing environment.
Full Job Description

Senior Process Engineer – Viral Vector

Houston, TX

The actual location of this job is in Houston, TX, USA. Relocation assistance is available for eligible candidates and their families, if needed.

This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will do:

  • Lead the support to manufacturing by troubleshooting equipment and process issues
  • Collaborate with Reliability engineer to improve equipment reliability and support maintenance programs.
  • Provide engineering support to production in the identification of new equipment suited to process requirements.
  • Monitor processes and lead the implementation of continuous improvement initiatives.
  • Lead failure analysis exercises and support corrective action implementation.
  • Own and drive change controls, deviations, and validation activities
  • Work with cross-functional teams to improve performance
  • Develop URSs, technical specifications, standards, drawings, SOPs, and documentation while supporting validation, audits, and continuous improvement efforts.

What we are looking for:

  • Bachelor degree in Chemical, Mechanical, Industrial, Electrical or related fields
  • 5-10 Years of experience in Pharmaceutical or Biotechnology Manufacturing
  • Strong troubleshooting, analytical, and problem-solving skills with the ability to improve processes, equipment performance, and automation functionality.
  • Ability to develop URSs, technical specifications, standards, drawings, SOPs, and documentation while supporting validation, audits, and continuous improvement efforts.
  • Must have a deep understanding of the principles of GEP/cGMP/GDP and how they are related to maintenance and documentation.
  • Must be able to work with minimum supervision
  • Must have excellent leadership skills
  • Able to record information accurately and write official documents.
  • Able to perform procedures according to written guidelines and recognize a deviation from accepted practice.
  • Able to use spreadsheets, databases and word processing software.
  • Able to effectively communicate with peers and supervisors verbally and in writing.
  • Able to multi-task and displays the effective use of time in managing projects.
  • Self-motivated, works well independently and as a team player.
  • Must have a deep understanding RCM and Total Productive Maintenance(TPM)
  • Understanding of process improvement and reliability engineering principles, methodologies and tools

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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