Careers At CQV Technologies
Validation Engineer
- 5 to 6 years of Process Validation (IQ, OQ & PQ) & test method validation experience
- Experience in process characterization, Gage R&R studies
- Knowledge in Statistical data analysis & Minitab
Design Control Engineer
- 6 years experience in Medical devices design & development, especially cardio vascular products
- Experience in working in Medical device – New product development & DHF Remediation projects
- Good understanding of ISO13485 & ISO14971 standards, 21 CFR Part 820 & EU MedDev Regulations
Risk Engineer
- 5 years experience in Medical devices design & development, especially cardio vascular products
- Good understanding of ISO13485 & ISO14971 standards
- Experie• 5 years experience in Medical devices design & development, especially cardio vascular products
Manufacturing Quality Engineer
- Provide support and leadership to team leaders, operator and support staff.
- Responsible for implementation of FMEA Control plans and other tools in the advance quality planning (APQP).
- Work with cross functional team to coordinate PPAP’s with OEM’s and suppliers.
Senior Design Engineer
- Experience in Medical Device Product Development
- Experience in coordinating with offshore teams, preferably experience of working with teams in India
- Expertise in CAD software UG NX and Teamcenter Engineering or similar CAD software is must
Quality/Validation Engineer
- B.S. in Computer Science, Software Engineering, MIS, or equivalent preferred
- 10+ years of experience as a Quality/Validation Engineer.
- Experience working in a regulated environment (SOX, HIPAA, CLIA, FDA)