*** Compañia Medica Ubicada en Otay, Busca, Ingeniero de Proyecto con Experiencia en Empaque****
****** Proyecto Temporal de 18 Meses con Opción que sea Permanente terminando el proyecto****
•Improve manufacturing processes using engineering methods (e.g., LEAN methods, basic statistics) for continuous process improvement
•Develop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
•Analyze and resolve basic Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
•Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
•Establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis)
•Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes
•Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
•Other incidental duties assigned by LeadershipI
Experiencia y requisitos:
• Bachelor's Degree or equivalent in Engineering or Scientific field Required
•Medical Device Manufacturing (ISO13485) – Preferred
•Good computer skills in usage of MS Office Suite including MS Project; CAD experience preferred (if applicable)
•Bilingual 80%
•Basic documentation, communication (e.g., written and verbal) and interpersonal relationship skills
•Basic understanding of statistical techniques
•Previous experience working with industrial equipment preferred (if applicable)
•Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
•Good problem-solving, organizational, analytical and critical thinking skills
•Good understanding of processes and equipment used in assigned work
•Knowledge of and adherence to Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
•Strict attention to detail
•Ability to interact professionally with all organizational levels
***** Interesados enviar C.V. ********** , especificando puesto de interes****