Automation Specialist for Medical Device Industry Transformation Lead
hace 2 días
V&EG is a leading services supplier providing solutions for Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries.
Key Responsibilities- Validate & Engineering Group’s solutions for Medical Devices industry
- Develop and execute Design Documentation (URS, DS), IQ, OQ, PQ protocols
- Generate deviations and reports, ensure SDLC, Risk Assessment, Data Integrity
- Participate in Factory Acceptance Test (FAT) & Site Acceptance Test (SAT)
- Conduct Technical Writing and investigations processes
- Bachelor's Degree in Computer Science or Engineering
- Minimum 8 years of experience in pharmaceutical, medical device or biotechnology industries
- Strong knowledge in cGxP and regulatory guidance
- Proficiency in Allen Bradley, Software Validation and Design Review
- Fully bilingual (English / Spanish) with excellent oral skills
- Proficient using MS Windows and Microsoft Office applications
Be part of a talented team committed to work under highest ethics standards.
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