Manufacturing Engineer
Job Description
We are seeking a motivated and detail-oriented Entry-Level Manufacturing Engineer to join our team. The ideal candidate will have up to 3 years of experience in manufacturing within the medical devices, biomedical, biotechnology, or pharmaceutical industries. This role involves supporting manufacturing processes, improving production efficiency, and ensuring product quality.
Key Responsibilities
We are seeking a motivated and detail-oriented Entry-Level Manufacturing Engineer to join our team. The ideal candidate will have up to 3 years of experience in manufacturing within the medical devices, biomedical, biotechnology, or pharmaceutical industries. This role involves supporting manufacturing processes, improving production efficiency, and ensuring product quality.
Key Responsibilities
- Assist in the design, development, and implementation of manufacturing processes for medical devices.
- Collaborate with cross-functional teams, including R&D, Quality Assurance, and Production, to support new product introductions and process improvements.
- Conduct tests and experiments to improve manufacturing processes, equipment, and products.
- Analyze production data to identify trends, root causes of issues, and opportunities for process optimization.
- Support the development and maintenance of standard operating procedures (SOPs) and work instructions.
- Participate in troubleshooting and resolving manufacturing issues to minimize downtime and ensure product quality.
- Ensure compliance with industry standards and regulations, including FDA, ISO, and GMP.
- Contribute to continuous improvement initiatives to enhance manufacturing efficiency and reduce costs.
- Bachelor’s degree in Manufacturing Engineering, Biomedical Engineering, Mechanical Engineering, or related field.
- 0-3 years of experience in a manufacturing environment within the medical devices, biomedical, biotechnology, or pharmaceutical industries.
- Experience with manufacturing processes, equipment, and quality control methodologies.
- Knowledge of regulatory requirements and standards (e.g., FDA, ISO 13485, GMP) is preferred.
- Strong analytical and problem-solving skills.
- Proficiency in using CAD software and other engineering tools.
- Excellent communication and teamwork abilities.
- Detail-oriented with strong organizational skills.
- Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.
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Seniority level
Entry level -
Employment type
Contract -
Job function
Engineering and Information Technology -
Industries
Biotechnology Research, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing
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