Job Title: Medical Device & Regulations, Camstar (Siemens Opcenter) Lead
Job Summary:
We are seeking a talented individual to join our team as a Medical Device & Regulations, Camstar (Siemens Opcenter) Lead. In this role, you will be responsible for overseeing the implementation and maintenance of Camstar (Siemens Opcenter) software in compliance with medical device regulations. You will work closely with cross-functional teams to ensure seamless integration of Camstar software into our operations.
Responsibilities and Duties:
- Lead the implementation of Camstar (Siemens Opcenter) software for medical device manufacturing processes
- Ensure compliance with medical device regulations, including FDA guidelines and ISO standards
- Collaborate with various departments to optimize the use of Camstar software for improved efficiency and quality
- Train and support end users on the use of Camstar software
- Troubleshoot and resolve any issues related to Camstar software
- Stay up to date on industry trends and best practices related to medical device regulations and Camstar software
Qualifications and Skills:
- Bachelor's degree in a related field (e.g. engineering, computer science)
- Experience working with Camstar (Siemens Opcenter) software in a medical device manufacturing environment
- Strong knowledge of medical device regulations, including FDA guidelines and ISO standards
- Excellent communication and collaboration skills
- Ability to work effectively in a fast-paced, team-oriented environment
- Problem-solving skills and attention to detail
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