Technician - mRNA Process Development

Accountability Cluster

Major Activities / Tasks

Accurate Execution of mRNA Production Processes

Perform IVT reactions

enzymatic processing

purification

Reliable Performance of Analytical Methods

Conduct standard analytical tests to monitor process performance

UV spectroscopy,

gel electrophoresis,

RNA quantification,

purity assessments

Maintenance of Laboratory Equipment and Work Areas

Operate, clean, and calibrate assigned instruments;

ensure workspaces remain organized and compliant with safety standards

Accurate Documentation and Data Recording

Perform analysis of in-licensed manufacturing process and identify optimization/improvement potential keeping process robustness in mind

Adapt in-licensed manufacturing processes and controls according to Cipla’s requirements harmonized with clinical development timelines including DNA process

Build plans for execution of implementation of improvements into in-licensed original process

Implementation of improvements in alignment with VP and CDO (mRNA)

Continuous improvement of CMC processes and analytics

Support for Process Optimization and Scale-Up

Assist scientists in

executing experiments,

collecting samples

compiling results for process improvement studies

Educational qualifications:

Completed vocational training as a Biological or Medical Technical Assistant (BTA or MTA)

Alternatively, a Bachelor's or Master's degree in biotechnology, biology, or a related life sciences discipline

Relevant experience:

5+ years of experience in process development or relevant field

Hands-on experience with IVT, enzymatic reactions, and purification processes including tangential flow filtration (TFF).

Familiarity with molecular biology tools, mRNA handling best practices, and aseptic techniques.

Strong organizational skills, attention to detail, and the ability to work both independently and in a team.

Ability to document and communicate effectively in English; German language skills are a plus.