Description:
We are currently recruiting for a number of roles in Wicklow. Our client is one of the leaders in global pharmaceuticals and is growing substantially. We are looking for a Senior Process engineer, Automation Engineers, Graduate Process Engineers, Project Engineers and QC Analysts to join this fantastic team. If you would like to learn more about this opportunity
Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services.
- Nearly $6 billion annual revenues
- 25 manufacturing sites around the world
- 10,000 employees worldwide of which 1,100 employees are committed to RandD
- This is permanent contract and comes with a very competitive benefits package;
- Salaries are negotiable based on level of role / experience.
- Yearly Target bonus (10%+)
- Annual salary review
- Private medical / Life assurance
- Contributory pension scheme
- Company shares scheme
- Enhanced holiday allowance
- Opportunities for progression
- Positive worker environment.
- Ensures manufacturing operations are continually supported and maintained in compliance with all quality, safety and environmental regulations.
- Technical transfer, Scale-up and Installation of new processes and new unit operations onto and with-in the plant.
- Support Process and Facility start-ups, initial campaigns and process optimisation.
- Complete detailed Equipment and Process assessments.
- Project Management of wide scope cross functional projects.
- Application of Six Sigma and Lean methodologies when undertaking projects and coaching others in use of these tools as part of their application.
- Ensure campaign preparations for individual processes are achieved to facilitate on‐time campaign start‐up and adherence of agreed production rate.
- Takes ownership for assigned process steps and provides process technical support as required.
- Lead cross functional investigations within operations. Use lean six sigma tools to drive root cause analysis and CAPA completion.
- The preparation and routine review of Batch Records, Cleaning Procedures, Equipment Operating Procedures, Standard Operating Procedures, Protocols and Summary Reports. These updates include actively making changes to drive improvements, increase in RFT and decrease in deviations.
- The development and update of control system recipes.
- Participation in audits, quality monitoring inspections and self-inspections as required. Lead cycle time reduction initiatives.
- Participation and driving of Continuous Improvement Activities.
- Lead EHS activities including Process HAZOP.
- Preparation of change control packages.