Description:

OncoBeta is a growing Medical Device start-up focused on developing and marketing a radionuclide powered therapy for non-melanoma skin cancer (NMSC), the world’s most common cancer. OncoBeta is changing the world’s standard philosophy related to skin cancer care. We stand for changing the status quo for the benefit of millions of patients worldwide.

OncoBeta is establishing its commercial footprint worldwide. Our European headquarters are in Munich, Germany, and we have affiliates in Europe, South Africa, and Australia

What to Expect:

Expect to work in a dynamic, transparent, open, friendly and international team. We are always aiming to do our best. Expect to push yourself and to grow as an individual. Expect to be treated fairly, with dignity and to be given significant responsibility and freedom to manage big initiatives.

Training will be provided where needed to ensure continued expertise in the below quality management frameworks. This is an opportunity to participate in the global expansion of an exciting medical device innovator.

This role reports directly to the Engineering Manager.

Responsibilities

• Co-lead projects related to the continued global scaling of OncoBeta’s manufacturing system (i.e. Production Line build outs in South Africa, Australia, and Europe, as well as other future markets)
• Co-manage production of application hardware systems and their deployment into treating clinics world-wide, as well as their maintenance over time
• Develop, evaluate, and improve manufacturing and operational processes
• Engage with external stakeholders in supply chain and hardware vendors’ network
• Contribute to future product design and R+D projects, including testing, scoping, budget characterization, and project management activities
• Engage in cross departmental projects, interacting with Marketing&Sales, Technical, and QMS
• Support the commercial team by attending conferences, give device demonstrations for new customers, and organize technical webinars
• Execute technical documentation, CAPAs, design work with CAD
• Creation and updation of technical documents, as per MDR and other applicable regional specific requirements
• Support in maintenance of QMS ISO 13485, knowledge of risk management according to ISO 14971 would be additional

Requirements and skills

• At least 3-4 years of relevant experience
• Excellent English required; fluent German a plus but not required
• Mechanical, Biomedical, Manufacturing, Industrial, or Design Engineering degree holders only
• Master’s Degree is preferred
• Passionate about Healthcare
• Willingness to travel
• Driver’s license

Market competitive salary with 30 days’ vacation as standard