- Navigate intellectual property considerations and ensure compliance with relevant regulations
- Ensure that designs are optimized for cost-effective and efficient manufacturing
- Apply deep knowledge of injection molding techniques and materials to optimize product designs
- Perform simulation and non-linear structural analysis (both static and dynamic) to validate product designs and improve performance.
- Execute, or review and interpret mold flow analysis data to enhance the quality and manufacturability of plastic components
- Collaborate with external CROs for the execution of Human factor studies and with external laboratories for setting up verification testing; review and approve protocols and reports
- Engage with stakeholders, including customers and regulatory bodies, to gather requirements and ensure product compliance
- Create and maintain comprehensive design documentation, including drawings, specifications, and reports
- Contribute to the transfer of the design to the development/manufacturing site
- Follow Company's Quality Policy and comply with current operational standards and legislative requirements
- Work in accordance with the requirements of the written Policies, Standard Operating Procedures, Technical Directives and Protocols of the company's Quality System, that are related to the duties of the described position
- Follow the rules of hygiene and control of health status as defined in the relevant Policies and Standard Operating Procedures
- Bachelor's or Master's degree in Mechanical Engineering or related field
- Minimum of 4-5 years of experience in medical device design, with a focus on drug delivery devices (particularly with a specialization in injectable devices)
- Experience working with industrial designers and medical device regulatory standards in either an in-house pharma role of with a manufacturer or design services company
- Excellent communication in English language (writing & speaking)
- Proficiency in 3D CAD software, particularly SolidWorks
- In-depth knowledge of injection molding, DFM, and mold flow analysis
- Strong understanding of intellectual property (IP) considerations
- Experience with Product Data Management (PDM) and Product Lifecycle Management (PLM) system
- Capability to conduct simulation and non-linear structural analysis
- Familiarity with simulation and non-linear structural analysis (static and dynamic)
- Exceptional understanding of injection molding techniques and materials
- Ability to comprehend and navigate the complexities of intellectual property issues Person Profile
- Self-sufficiency and ability to work independently.
- Strong communication skills, with the ability to effectively communicate in a cross functional basis
- Relationship driven – strong influence and interpersonal skills.
- Ability to work independently and collaboratively in a fast-paced environment
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Lead Design Engineer - Provincie Luxemburg, België - greenfield
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Beschrijving
We are pleased to present a unique opportunity with our client a leading generic pharmaceutical company with a global presence and who focus on research-driven innovation, high-quality manufacturing, and sustainable business practices to improve access to affordable healthcare worldwide.
The company operates state-of-the-art R&D facilities that adhere to stringent international quality standards. Boasting a diverse workforce employees from different cultures and locations. They are currently in a phase of continuous expansion meaning significant investments into cutting-edge Infrastructure and technology.Role Context:
To lead the design of drug delivery devices, focusing on plastic components, mechanisms, and assemblies with particular focus on innovation and advancement in the company's drug delivery technology.
Collaborating closely with cross-functional teams, including industrial designers, to create aesthetically pleasing and functional products.This is a newly created role in the business where historically this function has been outsourced to specialist engineering development companies It is envisaged that this role will be the foundation for the growth of a wider internal development team.
Role Profile:Role Requirements:
Athens, GR
Compensation:
a broad and extensive compensation package is available. International applications are fully encouraged from both EU/EEA and Worldwide. Relocation is supported by the employer.
Greenfield is a leading Luxembourg based Recruitment and Executive Search Consultancy and has been selected exclusively to fulfil this mandate.
