Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office
Job Description
Location/Division Specific Information
Thermo Fisher Scientific Inc. is currently seeking a Engineer III Automation Engineering for our Cincinnati facility. By joining our team you will have the opportunity to make a tangible difference and receive the appropriate support needed to accomplish your professional aspirations.
How will you make an impact
In this role you will not only be leading automation projects but also ensuring compliance with industry standards investigating system issues and documenting detailed deviation reports. Your deep understanding of automation technologies will be vital in maintaining the highest standards of quality and compliance in a regulated environment.
Must be available to support production during the established on-call schedule to allow for 24x6 site support.
What will you do
- Support for site automation and control systems. This includes design maintenance and monitoring of manufacturing control components and infrastructure to meet site manufacturing objectives.
- Take charge of automation projects from start to finish including planning implementation and validation. You will play a key role in developing and implementing creative solutions that will improve our manufacturing processes.
- Work closely with various teams to ensure successful project delivery and system integration. Your ability to collaborate effectively with different teams will be critical in achieving the integration of automation systems.
- Keep up-to-date with industry trends regulatory changes and advancements in automation for pharmaceutical manufacturing.
- Provide technical support and mentorship to other specialists and team members.
- Be available to support production during the established on-call schedule to allow for 24x6 site support.
Education:
- Bachelors degree in Engineering Computer Science or a related field or equivalent experience.
Experience:
- Minimum of 3 years of proven experience in automation engineering or controls equipment experience.
- Pharmaceutical industry experience preferred.
Knowledge Skills Abilities:
- Experience programming PLCs (RS Logix and FactoryTalk).
- Proven expertise in successfully leading automation and controls projects.
- Knowledge of computer system validation (CSV).
- Familiarity with FDA 21 CFR Part 11 Good Manufacturing Practices (GMP) and Good Automated Manufacturing Practice (GAMP).
- Ability to fix and resolve complicated problems within facilities manufacturing and other Engineering support areas.
- Ability to read and comprehend P&ID designs and documentation.
- Ability to work in a fast-paced results-orientated environment.
- Strong interpersonal and relationship building capability to establish and maintain effective working relationships with multi-functional teams contractors suppliers and clients.
- Experience with Rockwell Automation PharmaSuite platforms (preferred).
- Knowledge of pharmaceutical manufacturing processes and equipment (preferred).
Relocation assistance is NOT provided
Must be legally authorized to work in the United States without sponsorship now or in the future.
Must be able to pass a comprehensive background check which includes a drug screening.
Apply today!