Process Engineer
- Cork
- Contract
- CAPEX Projects
This vacancy has now expired
One of our global Pharmaceutical clients is looking for a Process Engineer to join their team close to the picturesque and historical city of Cork. The site is renowned for manufacturing excellence and plays a vital role in the company's large-scale biotech operations worldwide.
The site has received €130 million in investment over the last five years to continue the growth and expansion of the facility; with new products coming to the site, it is an exciting time to join the team.
Responsibilities & Requirements:
- Process optimisation: continually evaluate and optimise manufacturing processes to enhance efficiency, reduce waste, and minimise costs. Analyse data, collaborate with cross-functional teams, and identify areas for improvement to achieve operational excellence.
- Troubleshooting and problem-solving: Play a critical role in identifying and resolving issues in manufacturing processes. Analyse data, conduct root cause analysis, and develop and implement solutions to improve process performance and resolve bottlenecks.
- Process documentation: Responsible for creating and maintaining maintenance plans on SAP, and engineering standard operating procedures (SOPs), work instructions, and process flow diagrams.
- Continuous improvement: actively participate in continuous improvement initiatives and lean manufacturing practices. Collaborate with cross-functional teams to implement process improvements, such as implementing automation, reducing cycle times, and enhancing product quality.
- Quality control: work closely with quality teams to ensure that manufacturing processes comply with quality standards and regulations. QN and CAPA owner. Conduct audits with the quality team to identify opportunities for improvement.
- Project management: Lead or participate in projects related to process improvement, new product introduction, cost reduction, or capacity expansion. Coordinate project activities, set timelines, allocate resources, and ensure successful project implementation.
- EHS: Works closely with the EHS teams to ensure EHS compliance. Completes EHS investigation, CAPA owner and is Standard Owner for SN25 Hot Work.
If this role is of interest to you, please apply now!
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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