Osi Pi

**Job Summary**

**Responsibilities**
- Lead the development and implementation of Opcenter Execution Pharma solutions to meet client requirements.
- Oversee the technical aspects of projects ensuring high-quality deliverables and adherence to timelines.
- Provide technical guidance and mentorship to team members fostering a collaborative and innovative environment.
- Collaborate with cross-functional teams to design and optimize solutions that align with business objectives.
- Ensure the integration of Opcenter Execution Pharma with other enterprise systems enhancing overall efficiency.
- Conduct thorough testing and validation of solutions to ensure they meet regulatory and quality standards.
- Troubleshoot and resolve technical issues providing timely and effective solutions to minimize downtime.
- Develop and maintain comprehensive documentation for all technical processes and solutions.
- Stay updated with the latest industry trends and advancements in Opcenter Execution Pharma and Medical Devices.
- Participate in client meetings and presentations effectively communicating technical concepts and solutions.
- Contribute to the continuous improvement of processes and methodologies within the team.
- Ensure compliance with all relevant regulations and standards in the Medical Devices domain.
- Drive innovation and identify opportunities for leveraging new technologies to enhance solutions.

**Qualifications**
- Possess a strong technical background with 6 to 10 years of experience in Opcenter Execution Pharma.
- Demonstrate expertise in designing and implementing solutions in the Medical Devices domain.
- Exhibit excellent problem-solving skills and the ability to troubleshoot complex technical issues.
- Show proficiency in integrating Opcenter Execution Pharma with other enterprise systems.
- Display strong communication skills both verbal and written for effective collaboration and client interactions.
- Have a proactive and innovative mindset with a focus on continuous improvement.
- Demonstrate the ability to work effectively in a hybrid work model and day shift.
- Show a commitment to maintaining high-quality standards and regulatory compliance.
- Possess strong leadership and mentorship skills to guide and support team members.
- Exhibit a keen interest in staying updated with industry trends and advancements.
- Have experience in developing and maintaining technical documentation.
- Show a strong understanding of regulatory and quality standards in the Medical Devices domain.
- Demonstrate the ability to drive innovation and leverage new technologies for enhanced solutions.