Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our team at Thermo Fisher Scientific as a Process Engineer, where you'll contribute to our mission of enabling customers to make the world healthier, cleaner and safer. In this role, you'll support manufacturing operations by developing, optimizing and implementing production processes while ensuring compliance with quality standards. You'll collaborate with cross-functional teams to manufacture critical products for diagnostics, research, and therapeutic applications. The position offers opportunities to enhance processes, solve technical challenges, and directly impact patient care through high-quality manufacturing. Here is what is involved in the day-to-day:

• Acquiring a detailed understanding of the technical aspects of the process and the equipment and facilities.
• Providing technical support to the process to ensure that the customer requirements and site metrics are achieved.  Supporting performance management activities.
• Leading/contributing to troubleshooting activities and the resolution of technical investigations on plant.
• Supporting process start-up activities through generation of the relevant documentation
• Managing and seeking approval for all engineering change for the product and ensuring that this is appropriately communicated on site. Close out all change controls in a timely fashion. Ensure all engineering changes made have safety and quality considerations as core attributes.
• Completing end of campaign after action reviews (AARs) to capture key learnings and actions required prior to next campaign and seeking input from all relevant personnel within the value stream.
• Supporting the screening and quotation process for the Cork site as required.
• Supporting any outsourcing ventures as required being accountable for successful transfer of the product technical knowledge.
• Providing technical support for product changeovers. Complete cleaning calculations as needed. Support the completion of the relevant cleaning risk assessments.

REQUIREMENTS:

• Bachelor's degree required: Preferred Fields of Study: Chemistry, Biochemistry, Chemical Engineering, Biotechnology, or related scientific field
• Working knowledge of GMP, GDP, and other relevant regulatory requirements
• Strong technical writing skills for SOPs, batch records, and investigation reports
• Proficiency in Microsoft Office applications
• Strong analytical and problem-solving abilities
• Effective communication skills and ability to work collaboratively in teams