Aktuelle Jobs im Zusammenhang mit MSAT LM DP Senior Technical Lead - Schaffhausen, Schaffhausen - Johnson & Johnson
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MSAT LM DP Senior Technical Lead
vor 2 Monaten
The Principal Engineer plays a pivotal role in the development and implementation of robust manufacturing process design solutions for Primary Packaging Components and Closure Systems. This strategic role requires collaboration with cross-functional teams, including R&D, Procurement, and Make Functions, as well as external partners, to meet the emerging and future needs of the portfolio.
As a Principal Engineer, you will be responsible for the technical development, life cycle management, and manufacturing readiness of primary packaging components and their interdependencies to the devices within the Johnson & Johnson manufacturing network.
You will lead and contribute to complex projects, ensuring the successful design, development, validation, and transfer of medical devices to support the global device platform, ensuring adequate capacity and capability for supply of medical devices used in drug/device combo products.
Key Responsibilities:
- Strategic leadership for primary container stronghold, operating and managing a global network within a matrix organisation.
- Provide subject matter expertise to the manufacturing strategy, control strategy of primary packaging components with the supplier and embed them into the manufacturing control strategy of the Make functions.
- Lead process design and characterization studies, primary packaging Life cycle management and major investigations and improvements plans.
- Contribute to supplier selection process by providing technical leadership and assessments.
- Partner with receiving sites to ensure voice of manufacturing is represented in product design (e.g., design for manufacturability).
- Partner with external suppliers to ensure component development processes lead to robust manufacturing processes.
- Provide technical expertise to site personnel to adequately transfer the Primary packaging material for design and technology transfer activities.
- Contribute to develop manufacturing process capacity scale-up for internal and external manufacturing.
Qualifications:
- Master's in engineering or science required, with a preference for Mechanical, Biomedical, or Materials.
- A minimum of 10 years' experience in some aspects of medical device design, development, new product introduction and/or technical support.
- Fluent in English, German is a plus.
- May require up to 15% travel.
- Experience in communicating across various levels of an organization is required.
- Must be able to manage multiple priorities, maintain confidentiality, and operate with poise and professionalism in a complex, high-profile, and rapidly changing environment.
- Excellent organizational and planning skills, strong interpersonal, verbal, and written communications skills. Demonstrates strong collaboration with colleagues.
- Experience in primary packaging components (Syringe, vials, cartridge) is desired. Design for manufacturability and assembly experience is required.
- Plastic and metals materials and processing technologies is preferred, Knowledge & expertise in applying Combination Products cGMP regulations is preferred.
