Today, Lonza is a global leader in life sciences operating across three 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.
The MES Engineer Level 3 is responsible for driving and leading activities such as requirements gathering, authoring, testing, implementation and use of Manufacturing Execution Systems (MES). Position is expected to operate with a high degree of autonomy with only general supervision.
Develop technical knowledge on manufacturing equipment and process automation systems
Manage resolution of equipment breakdowns and quality issues in the suites
Provide SME support to Manufacturing and other departments for the design and operation of process automation equipment
Conduct troubleshooting and technical analyses on manufacturing equipment and process automation systems including PI data analyses, CIP/SIP circuit review, flow path analyses, code review/troubleshooting, etc.
Assist with tech transfer of new processes into the facility
Complete change request lot assessments to support lot release
Participates in IPT/JPT meetings and customer ad hoc meetings as MES SME
Represents group at MES DMS meetings
Participates in audits and inspections as MES SME
Planning and execution of plant projects involving complex automation changes and significant process improvements including lump sum capital projects
Execute test scripts (design , execution, simulation, wet testing)
Own change requests and complete change request tasks to support project completion
Perform change request assessments
Deviations / RCAs
Assist the Quality department with deviation investigations
Performs MES review/approval of deviations
Participate in RCAs as MES representative
Owns and executes completion of CAPA actions
Participates in quality risk assessments
Review/revise MES and Manufacturing related SOP’s, Functional Specifications, and work instructions as a result of CAPA, equipment/process changes, error prevention activities, etc.
Complete MES review/approval of batch records, deviations, commissioning protocols, and validation protocols
Performs all work safely and meets the requisite training requirements.
Bachelor’s degree in science, technology, engineering or mathematics.
Syncade Recipe Authoring experience strongly preferred.
Experience working in automation in a Pharm/Biotech environment.
Advanced Recipe Author (in Syncade).
Effective communication at all levels.
Ability to secure relevant information and identify key issues and relationships from a base of information.
Evaluate engineering problems and be able to devise cause and effect relationships and propose solutions.
Adapt to changing conditions.
Ability to prioritize deliverables.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if it is not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.