This role plays a vital part in the Product Supply Units team, contributing to the reliable supply of syringe and vial products worldwide.
Job Description
As a Process Engineer, you will be responsible for providing technical support to the Product Supply APU. Your focus will be on delivering continuous improvement projects for existing equipment, collaborating with various departments such as MSAT, Technical Development, Quality Assurance, and Supply Chain.
You will lead and coordinate elements of automated inspection projects, contribute to process engineering activities related to the development of new and existing manufacturing capacity, and ensure safety compliance by identifying and implementing process and product improvements.
Your expertise will also be utilized to analyze machine performance data, manage improvement projects within budget and time constraints, and support new product introductions and capacity expansions.
Required Skills and Qualifications
* Degree in an Engineering discipline (Mechanical, Manufacturing, Chemical, Industrial, Biomedical, etc.)
* Experience in a GMP-regulated pharmaceutical, biotech, or medical device environment, preferably supporting sterile manufacturing or fillfinish processes
* Hands-on experience with automated or semi-automated equipment; exposure to PLCs, sensors, robotics, or vision systems (AVI experience desirable)
* Strong process engineering skills, including troubleshooting, deviation investigations, CAPA, and data analysis
* Familiarity with qualification/validation (IQ/OQ/PQ), change control, and technical documentation
* Understanding of inspection, assembly, labelling, or packaging technologies for prefilled syringes, vials, or related products
Benefits
This role offers an excellent opportunity to gain experience in the biopharmaceutical industry with an award-winning organization. You will have the chance to work closely with various departments, develop your skills, and contribute to the company's success.