Description

In this role, you will be at the forefront of producing recombinant products, operating automated equipment, and ensuring compliance. Your daily responsibilities will include supporting new production lines, maintaining training records, and actively contributing to operational excellence initiatives.

Requirements

• •Adherence to Good Manufacturing Practices (GMP) Safety Standards
• •Bachelor/Master in Chemistry, Biochemistry, Biology, or Food Science
• •3-5 years of experience in pharmaceuticals operations in a GMP environment
• •Experience in biotech or pharma processes, including sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
• •Willingness to learn
• •Can-do attitude
• •English and German language skills preferred

Tasks

• •Operate automated production equipment for recombinant products
• •Support compliance, scheduling, and material management
• •Assist with change controls and investigations
• •Contribute to CAPA and operational excellence initiatives
• •Support project teams in designing and commissioning new production lines
• •Facilitate the start-up of new production lines
• •Execute daily manufacturing activities in USP, DSP, or support areas
• •Prepare media and buffers, and clean and prepare equipment
• •Serve as the first point of contact for training and troubleshooting
• •Maintain Work Instructions and SOPs in the area
• •Investigate Manufacturing Excellence initiatives for smooth operations
• •Define robust process parameters during manufacturing campaigns
• •Participate in New Product Introduction activities
• •Ensure training and compliance records are up to date
• •Commit to Thermo Fisher Scientific values and ethical standards
• •Take accountability for presence, performance, and productivity
• •Adhere to EHSS legal requirements and policies
• •Contribute to EHSS initiatives and report near misses