What are the responsibilities and job description for the Process Engineer position at cGxPServe?
Job Summary :
We are seeking a skilled and detail-oriented Process Engineer with an electrical or mechanical engineering background to join our team.
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.
Responsibilities :
Ensure that the transferred process is adhering to the Device Master Record.
Analyze current manufacturing processes and create detailed documentation to facilitate the transfer of medical devices to new facilities.
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.
Ensure all transferred processes comply with relevant industry standards, regulatory requirements, and quality assurance protocols.
Evaluate existing equipment and technologies to determine compatibility at the receiving facility; recommend upgrades or changes if necessary.
Ensure that equipment qualification is in compliance with the product requirements.
Provide training and support to facility teams to ensure they are equipped to manage new processes effectively.
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.
Requirements :
A bachelor's 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.
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.
Skills :
Engineering Electrical or Mechanical preferable.
Medical Device experience in manufacturing : preferably electrical mechanical devices.
Transfer of products it could be experience of product transfer from R&D to manufacturing or product transfer from site to site.
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