Manufacturing Engineer
4 weeks ago
Responsibilities:
- Extensive knowledge of assembly and assembly related technology.
- Be proficient on time/motion methods and studies.
- Assemble effective multi-discipline core team members and effectively lead team activities.
- Coordinate the acquisition of data to initiate and complete improvement projects.
- Perform ergonomic analysis, justify, and implement improvement activities.
- Coordinate purchase evaluate of new / existing equipment/system from design and implementation phase to ensure proper integration with human elements and budgetary compliance including new program launches.
- Write & coordinate to complete validation protocols, procedures and final reports for new equipment & processes to support customer & internal requirements.
- Work closely with operations to ensure operators are properly trained on processes required for production of new / existing components.
- Evaluate material and information flow and identify areas of improvement includes creation of parts & inputting Bill of Materials (BOMs).
- Interface with users of systems to identify current issues and identify/justify/coordinate improvement activities.
- Standardize raw material, equipment, and documents with objective of mitigating, reduction, and prevention of variation within processes.
- Reduce inventory loss of finished goods, purchased components and maintaining or improving inventory accuracy targets.
- Evaluate and implement proposed/required changes on manufacturing process related documents.
- Ability to design, build & modify basic fixtures or equipment, automated systems, poke yokes etc. for best practices & continuous improvement initiatives.
- Supports / keeps up to date with both existing & new automation technology with component & process upgrades.
- Performs training of technical staff to support maintain manufacturing related equipment which includes automated systems, robotic applications, programmable controllers etc.
- Develop visual systems to facilitate management by Visual Management.
- Participates/leads proactive continual improvement efforts using multi-disciplinary teams.
- Supports / participate in corrective action activities.
- Effectively apply PDCA (plan, do, check, action) in all aspects of job.
- Perform plant layout analysis by working directly with manufacturing on workplace layouts, manning requirements, material flow & processes along with various other activities (i.e., performance of time study analysis, task inventories, standard work content charts and ergonomic reviews) make recommendations, develops, and implements plans for new / existing model programs.
- Performs training of technical staff to support maintain manufacturing related equipment which includes automated systems, robotic applications, programmable controllers etc.
- Supports / keeps up to date with both existing & new automation technology with component & process upgrades.
- Requires a bachelor’s degree in engineering in Mechanical Engineering, Industrial Engineering or Biomedical Engineering is preferred.
- A minimum of 5 years’ experience in product quality within the medical device industry is preferred.
- Previous knowledge and experience in manufacturing processes of chemicals & plastics is preferred.
- Computer skills including Microsoft Office and Manufacturing Management products.
- Must be familiar with cGMP requirements.
- Recommended to have experience with EPA, FDA regulations (i.e. 21 CFR 820)
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