Project Manager - Manufacturing Engineering
Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
The Opportunity
Leading the process/machine technology and -automation in CAPEX projects by acting as (sub-)project lead for the area of manufacturing engineering in a GMP environment
Leading external workforces for planning, construction, commissioning, qualification & validation within CAPEX projects
Ensuring engineering quality by selecting appropriate suppliers, managing procurement and performing claim management
Ensuring quality, costs and timelines: develop detailed project plans, manage timelines and ensure project milestones are met
Translation of user requirements into technical solutions
Implementation of change management where necessary
Oversee the integration and communication between machine automation, PCS and MES
Who you are:
Completed Technical studies (Bachelor required, Master preferred) in the field of engineering, preferably mechanical engineering and/or automation technologies
Min. 5 years of proven experience in project engineering, preferably within the manufacturing sector
Proficiency in machine automation, PCS, MES, and IT infrastructure
Strong understanding of interface management
Excellent project management skills with the ability to handle multiple projects simultaneously
Communication: Strong interpersonal and communication skills to effectively collaborate with diverse teams
Knowledge of cGMPs, GAMP or equivalent regulations. Experience working in a regulated environment, knowledge of cGMPs, and a strong understanding of the regulatory requirements specific to aseptic processing
Knowledge of legal and regulatory requirements and standards in practice
This role is graded at SE6, however the final grade would be evaluated on an individual basis.
This is an amazing opportunity to work within an innovative and inclusive environment, with emphasis on personal and professional growth. Apply to be considered.
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche Diagnostics International in Rotkreuz is a leading provider of diagnostic systems solutions, and the largest manufacturer of fully automated in vitro diagnostic systems in Switzerland. We are more than 2’700 passionate colleagues from over 65 nationalities. Find out more about our site in Central Switzerland, here.
Besides extensive development and training opportunities, we offer flexible working options, 18 weeks of maternity leave and 10 weeks of gender independent partnership leave. Our employees benefit from multiple services on site such as child-care facilities, medical services, restaurants and cafeterias, as well as various employee events.
We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche.
Roche is an Equal Opportunity Employer.