Contribute to Groundbreaking Biopharmaceutical Projects
Join a dynamic team at a leading Contract Manufacturing Organisation to support manufacturing operations in a biopharmaceutical environment. This role offers the opportunity to contribute to cutting-edge solutions and continuous improvement initiatives while ensuring strict compliance with industry standards.
Primary Responsibilities
- Prepare media and buffer solutions for production processes.
- Operate Clean-in-Place (CIP) and Steam-in-Place (SIP) systems.
- Assemble and operate filtration systems.
- Utilize general production equipment such as pH and conductivity meters, autoclaves, and portable mixers.
- Monitor and record critical process parameters.
- Complete all relevant documentation in compliance with GDP and GMP guidelines.
- Perform routine maintenance and cleaning of production equipment to ensure GMP standards are met.
- Conduct sampling using aseptic techniques.
- Participate in Continuous Improvement Teams to enhance processes.
- Receive and distribute supplies into production areas as needed.
- Train and mentor team members to foster skill development.
- Assist in troubleshooting process issues and responding to alarms.
- Perform other duties as assigned.
Skills and Requirements
- High school diploma or GED required; candidates with higher education are welcome to apply.
- Related experience is beneficial but not mandatory.
- Strong attention to detail and ability to follow strict protocols.
- Familiarity with GMP and GDP guidelines is advantageous.
- Willingness to work rotating 12-hour shifts.
- Effective communication and teamwork skills.
- Ability to perform physical tasks, including equipment assembly and cleaning.