Advanced Automation Professional for Healthcare Systems
hace 3 días
Our company seeks an experienced automation specialist to lead our team in developing cutting-edge medical devices.
Responsibilities:- Design and implement automated systems for medical devices, ensuring compliance with industry regulations.
- Collaborate with cross-functional teams to identify opportunities for process improvements and automation.
- Develop and execute comprehensive test plans to validate system performance.
- Provide technical guidance and support to junior team members to help them grow professionally.
- Bachelor's Degree in Computer Science, Engineering, or related field.
- Minimum of 8 years of experience in automation and software development.
- Strong understanding of medical device regulations and industry standards.
- Excellent communication and problem-solving skills.
- Ability to work effectively in a fast-paced environment.
Validation & Engineering Group, Inc. (V&EG) is a reputable service provider with extensive experience in providing innovative solutions for various industries.
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Parroquia La Unión, Venezuela Veg Group A tiempo completoLL02-020924 Sr. Automation Specialist (Medical Devices)Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other...
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Parroquia La Unión, Venezuela Veg Group A tiempo completoAbout Veg GroupVeg Group is a leading services supplier who provides solutions for various industries including Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices. Our expertise lies in Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.Job Description: We are seeking a highly skilled and...
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Parroquia La Unión, Venezuela Veg Group A tiempo completoJob Title: Senior Automation Specialist for Medical DevicesWe are seeking a skilled and dedicated individual who is committed to upholding the highest ethical standards in this role.Key Responsibilities:Develop and execute comprehensive Design Documentation (URS, DS), IQ, OQ, PQ protocols within direct pharmaceutical, medical device or biotechnology...
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