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Manufacturing process optimizer

Cork
beBeeProcessEngineer
Manufacturing
Posted: 27 June
Offer description

Optimize Manufacturing Processes as a Key Player

Join a global leader in medical device manufacturing and take on the challenge of optimizing critical manufacturing processes. This is a 12-month contract opportunity to make a lasting impact on patient outcomes through enhanced product quality and process efficiency.

Key Responsibilities:

- Investigate process performance, identify root causes of issues, and implement corrective actions.

- Drive continuous improvement initiatives to enhance process capability, yield, and efficiency.

- Support validation activities including process qualification, equipment validation (IQ/OQ/PQ), and test method validation.

New Product Introduction:

- Collaborate with R&D, Quality, and Manufacturing teams to ensure seamless integration of new products into commercial production.

- Support process development, scale-up activities, and manufacturing readiness for product launches.

Documentation & Compliance:

- Develop and update technical documentation, including manufacturing instructions, process flows, risk assessments, and validation protocols.

- Ensure all activities comply with FDA regulations, ISO standards, and internal quality systems (QMS).

Troubleshooting & Technical Support:

- Provide front-line technical support to manufacturing operations.

- Perform root cause analysis and implement effective long-term solutions.

Project Management:

- Support capital equipment projects including process definition, vendor engagement, and installation.

- Coordinate with suppliers, contractors, and internal teams to meet project milestones and quality requirements.

Requirements:

- Bachelor's degree in Engineering (Mechanical, Biomedical, Chemical, or related field).

- 3+ years' experience in a regulated manufacturing environment, preferably medical devices or pharmaceuticals.

- Strong understanding of FDA regulations, ISO 13485, and cGMP principles.

- Demonstrated experience in process validation, statistical analysis (DOE, SPC), and technical problem solving.

- Experience with equipment installation, process automation, and lean manufacturing principles is desirable.

- Excellent communication and cross-functional teamwork skills.

- Familiarity with Design Control and Risk Management (FMEA, pFMEA) processes.

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