Biopharma Manufacturing Technician - 12h Rotating Shifts

Proclinical; Schwyz; On-site; CHF 23,000 - 32,000; Full time

Job summary

Proclinical is seeking a Manufacturing Technician to support biopharma manufacturing operations. The role involves preparing media/buffer solutions, operating CIP/SIP systems, and ensuring GMP/GDP compliance. Flexible to rotate 12-hour shifts and contribute to continuous improvement.

Key responsibilities include equipment operation, documentation, sampling, and maintenance. Collaboration with teammates and adherence to strict protocols are essential to success in this role.

Qualifications

• 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.

Responsibilities

• Prepare media and buffer solutions for production processes.
• Operate CIP and SIP systems.
• Assemble and operate filtration systems.
• Use production equipment such as pH and conductivity meters, autoclaves, and portable mixers.
• Monitor and record critical process parameters.
• Complete documentation in line with GDP and GMP guidelines.
• Perform routine maintenance and cleaning of production equipment to meet GMP standards.
• Conduct sampling using aseptic techniques.
• Participate in Continuous Improvement Teams to enhance processes.
• Receive and distribute supplies to production areas as needed.
• Train and mentor team members to foster skill development.
• Assist in troubleshooting process issues and responding to alarms.

Skills

Attention to detail

GMP knowledge

Teamwork

Communication

Physical stamina

Shift flexibility

Education

High school diploma

Job description

Proclinical is seeking a Manufacturing Technician to support biopharma manufacturing operations. The role involves preparing media/buffer solutions, operating CIP/SIP systems, and ensuring GMP/GDP compliance. Flexible to rotate 12-hour shifts and contribute to continuous improvement.

Key responsibilities include equipment operation, documentation, sampling, and maintenance. Collaboration with teammates and adherence to strict protocols are essential to success in this role.