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As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual.
What you'd do
- Preparing and executing engineering documentation, operating procedures, maintenance procedures, and commissioning and validation test plans for utility and/or process systems.
- Demonstrate an understanding of basic project management skills.
- Mechanical aptitude and knowledge of biopharmaceutical manufacturing equipment, process, scientific instruments, and computer systems is required.
- Develop and implement tools for measuring, tracking, and improving standards compliance.
- Demonstrate communication and collaboration skills across functions.
- Assist in pulling, validating, and verifying data from various sources.
- Perform data entry tasks accurately and efficiently. Maintain and update databases and spreadsheets.
- Support administrative tasks such as scheduling meetings, organizing files, and preparing documents.
- Handle communication with internal teams and external vendors as needed.
- Participate in testing and troubleshooting of systems related to process engineering and instrumentation.
What they want
- Currently pursuing a BS or MS degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, or related engineering major.
- Have a cumulative GPA of 2.8 or higher, which is reflective of all college coursework.
- Strong analytical skills and attention to detail.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
- Excellent organizational and time management skills.
- Strong verbal and written communication skills.
- Ability to work independently and as part of a team.
- Basic understanding of large molecule drug manufacturing processes is a plus.
- Starts
- 2026-09-14