Manufacturing Process Specialist
17 hours ago
Russell Taylor Group Ltd is a global medical devices company seeking an experienced Process Engineer to join their team in Coventry. As a key member of the Operations department, you will play a vital role in developing and implementing process strategies, optimizing current processes, and maintaining process documents.
The ideal candidate will have significant experience working within a Med Device setting (ISO 13485/GMP) or similar, with a background in chemical engineering or a related field. Experience in process validation, scale-up, design transfer, and project management is highly desirable.
Salary Range: £60,000 - £80,000 per year
About the Role
In this exciting opportunity, you will be responsible for preparing process documentation and operating instructions, overseeing and assessing new and existing processes, meeting with production managers to assess existing processes, devising and implementing new strategies to optimize productivity, analyzing data to discover areas that need improvements, assessing compliance and adherence to safety and quality standards, performing risk assessments, and collaborating with maintenance, RAQ, R&D, and Commercial teams to support new product launches.
Key Responsibilities:
- Develop and implement process strategies, optimize current processes, and maintain process documents.
- Prepare process documentation and operating instructions.
- Oversee and assess new and existing processes and workflows.
- Meet with production managers to assess existing processes.
- Devise, implement, and test new strategies to help optimize productivity.
- Analyze data to discover areas that need improvements and upgrades.
- Assess compliance and adherence to safety and quality standards and report findings and proposals to higher management.
- Perform risk assessments.
- Work with maintenance, RAQ, R&D, and Commercial teams to support new product launches.
- Develop and implement metrics to monitor and improve performance of processes.
Requirements:
- Significant experience working within a Med Device (ISO 13485/GMP) or similar setting; chemical background considered.
- Experience in process validation.
- Experience in process scale up and design transfer and project management.
- Experience in lean principles and written validations (IQ, OQ, PQ, Kaizen, FMEA, etc.).
About Us
Russell Taylor Group Ltd is committed to providing equal opportunities to all candidates and adheres to fair employment practices.
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