Jr. Design Engineer

Position:

Job Summary:

Key Responsibilities:

• Design and develop components and assemblies for pharmaceutical machinery, ensuring adherence to project specifications and timelines.
• Use SOLID EDGE to create 2D drawings, 3D models, and detailed engineering designs for machine components and systems.
• Collaborate with senior design engineers to refine designs, troubleshoot issues, and implement improvements.
• Conduct design calculations, simulations, and testing to ensure functionality, performance, and safety.
• Assist in the preparation of technical documentation, including design specifications, BOM (Bill of Materials), and manuals.
• Participate in design reviews and provide support for prototype development and testing.
• Ensure compliance with industry standards, regulations, and company policies in the design process.
• Provide assistance in the selection of materials and components for machine construction.
• Support the manufacturing team with design clarifications and revisions as needed during the production phase.
• Work closely with cross-functional teams including R&D, production, and quality assurance.

Key Skills & Qualifications:

• Bachelors degree in Mechanical Engineering or a related field.
• Hands-on experience with SOLID EDGE software (preferred) or other similar 3D CAD tools.
• Understanding of mechanical design principles, including material selection, mechanical systems, and tolerances.
• Familiarity with the pharmaceutical industry and machinery (preferred but not required).
• Strong problem-solving skills and attention to detail.
• Ability to work in a collaborative team environment while also being able to work independently.
• Good communication skills, both written and verbal.
• Willingness to learn and adapt in a fast-paced, technical environment.

Preferred Skills (not mandatory):

• Experience in the design of machines or systems for the pharmaceutical industry.
• Basic knowledge of design for manufacturability (DFM) and assembly.
• Experience with other CAD software, such as AutoCAD, CATIA, SolidWorks or SOLID EDGE.
• Knowledge of regulatory requirements in the pharmaceutical manufacturing industry (e.g., GMP, FDA standards).