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.
Own and manage Mfg. process specific change controls, and CAPA’s and/or support operational readiness/tech transfer activities.
Drive and own improvement projects that support KPI’s, with a focus on cost, innovation, on-time delivery
and quality.
Manage projects from concept to completion; create and manage project plan, work cross- functionally to ensure right first time and provide adequate training to impacted areas.
Generate and Manage Metrics
Completion of Laboratory Investigation Reports. Perform Validation Protocol Review
Monitor Manufacturing CAPA due dates and support closure and extensions as needed
Minimum Required Qualifications/Skills:
AS/BS in Biotechnology, Biology, Chemistry, or equivalent
Preferred area of study: Science related discipline
High School Diploma or Equivalent may be considered with relevant experience
5-7 years Biotechnology, preferably Upstream and Downstream, or similar Manufacturing industry. (10+
years’ experience without AS/BS)
Excellent written (especially technical writing) and verbal communication