Production Optimization Expert

2 days ago


Stockholm, Stockholm, Sweden PharmaRelations ApS Full time
Senior Production Process Engineer

We aim to push the boundaries of medical device manufacturing excellence, and we need passionate professionals like you to help us achieve this vision.

In this pioneering role, you will lead the development, optimization, and validation of manufacturing processes for implantable Class III medical devices, fostering close collaboration with cross-functional teams.

You will champion the implementation of advanced manufacturing techniques, drive continuous improvement initiatives, and ensure compliance with regulatory standards.

To excel in this position, you must possess a strong background in process development and a genuine interest in driving innovation in medical device manufacturing.

Key Responsibilities:
  1. Process Development:
    • Develop and optimize manufacturing processes for new and existing implantable medical device products.
    • Collaborate with manufacturing teams and alliance partners on production development, technology transfer, and process implementation.
    • Design, document, and maintain process workflows, control plans, and standard operating procedures.
  2. Process Validation and Qualification:
    • Conduct process validation activities, including IQ/OQ/PQ for new and modified manufacturing processes.
    • Evaluate validation protocols against regulatory standards and execute effectively to meet quality requirements.
    • Analyze and document validation results, addressing any deviations or non-conformances.
    • Collaborate with maintenance and equipment teams to ensure optimal performance of manufacturing equipment.
  3. Continuous Improvement and Optimization:
    • Identify and lead continuous improvement projects to enhance process efficiency, reduce waste, and improve product quality.
    • Lead root cause analyses for process failures or deviations, implementing corrective and preventive actions as necessary.
    • Work closely with cross-functional teams to align on process requirements and project timelines.
    • Provide technical expertise and training to manufacturing staff on new processes, equipment, and quality standards.
  4. Regulatory Compliance and Documentation:
    • Ensure all production processes comply with medical device regulations and standards.
    • Maintain comprehensive documentation related to process design, validation, and improvement activities.
    • Participate in audits and regulatory inspections, providing technical support and documentation as required.
  5. Equipment Management:
    • Collaborate with maintenance and equipment teams to ensure optimal performance of manufacturing equipment.
    • Support the installation and validation of new equipment, ensuring it meets process requirements and regulatory standards.


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