BEPC Inc. - Business Excellence Professional Consulting
7 months ago
Validation Engineer (Medical Industry)
Sign up to save this job, get alerts, and apply with an optimized CV.
Company information
- Company
- BEPC Inc. - Business Excellence Professional Consulting
- Location
- México Mexico
- Posted
- 7 months ago
Job description
BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe. BEPC Inc. is seeking a Validation Engineer I to join our fast-growing team of consultants in the Ciudad Juárez area. This position provides technical engineering support to clients in the medical industry, focusing on validation and verification activities related to medical devices and equipment. The ideal candidate will have experience working with regulatory agencies such as FDA and ISO 13485, and be familiar with industry standards and guidelines for medical device development and testing. Responsibilities include: * Conducting risk assessments and failure mode effects analysis (FMEA) to identify potential risks and failures in the design and manufacturing process of medical devices. * Developing and implementing test plans and procedures to verify the performance and functionality of medical devices. * Collaborating with cross-functional teams, including engineering, quality, and manufacturing to ensure compliance with regulatory requirements and industry standards. * Providing technical support and guidance to clients on validation and verification activities related to medical devices and equipment. * Staying up-to-date with industry trends, regulations, and best practices in the medical device industry. Requirements: * Bachelor's degree in Engineering or a related field (Mechanical, Electrical, Biomedical). * 2+ years of experience working in the medical device industry, preferably in validation and verification activities. * Strong understanding of regulatory agencies such as FDA and ISO 13485. * Familiarity with industry standards and guidelines for medical device development and testing. * Excellent communication and interpersonal skills. * Ability to work independently and as part of a team. Benefits: * Competitive salary and benefits package. * Opportunities for professional growth and development in the medical device industry. * Collaborative and dynamic work environment. * Flexible working hours and remote work options.
Required skills
Interested in this position?
Create your free account and tailor your CV to match this job.