About the role
What you will do?
- Operate and monitor chemical processing equipment following established procedures
- Perform in-process quality controls, sampling, and data analysis according to specifications
- Identify and resolve process deviations, equipment failures, and safety hazards
- Record production data and documentation in regulatory compliance
- Collaborate with manufacturing, quality, maintenance, and engineering teams to resolve issues
- Diagnose technical problems and document root causes and corrective actions
- Support equipment installation, validation, maintenance, and cleaning
- Participate in continuous improvement initiatives approved by management
What you need?
Required:
- Associate's degree in Chemistry, Microbiology, or a related technical field, or a minimum of 3 years of experience in the medical device industry or in a regulated environment
- Basic English: ability to read and comprehend technical and safety documentation
- Basic math skills for calculations and measurements
- Ability to follow written and verbal instructions in a production environment
Desirable:
- Minimum 1 year in a GMP laboratory or similar
- Experience with laboratory equipment and reading technical specifications
Additional Information
- Physical requirements: Frequent lifting of 10–50 lbs; repetitive motion and variable postures
- Environment: Mandatory use of PPE in designated areas; exposure to machinery and noise