Senior Process Engineer III
Senior Process Engineer III
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Salary Not Disclosed
1 Vacancy
Job Description
- Design History File: Ensure that the transferred process is adhering to the Device Master Record.
- Process Analysis and Documentation: Analyse current manufacturing processes and create detailed documentation to facilitate the transfer of medical devices to new facilities.
- Transfer Planning: Develop and implement a comprehensive transfer plan including timelines resources and risk assessments to ensure smooth transition between facilities.
- Cross-functional Collaboration: Work closely with cross-functional teams including R&D Quality Assurance Regulatory Affairs and Supply Chain to align objectives and address any challenges during the transfer process.
- Regulatory Compliance: Ensure all transferred processes comply with relevant industry standards regulatory requirements and quality assurance protocols.
- Equipment and Technology Alignment: Evaluate existing equipment and technologies to determine compatibility at the receiving facility; recommend upgrades or changes if necessary.
- Process Validation: Ensure that equipment qualification follows the product requirements.
- Training and Support: Provide training and support to facility teams to ensure they are equipped to manage new processes effectively.
- Continuous Improvement: Identify opportunities for process optimization and efficiency improvements before and after the transfer.
- Reporting and Documentation: Maintain detailed records of transfer activities and provide regular reports to management on progress risks and outcomes.
- A bachelors degree in electrical engineering mechanical engineering or a related field.
- Minimum of 8 years of experience in process engineering preferably within the medical device industry.
- The successful candidate will be responsible for overseeing the transfer of medical device manufacturing processes from one facility to another ensuring seamless operation compliance with regulatory standards and minimal disruption to production schedules.
- Proven experience in transferring manufacturing processes between facilities.
- Strong knowledge of regulatory requirements and quality standards for medical device manufacturing.
- Excellent project management and organizational skills.
- Ability to work independently and collaboratively in a fast-paced environment.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
Employment Type
Full Time
