Downstream Manufacturing Scientist in New Jersey

Global Life Science Hub are seeking a Downstream Manufacturing Scientist who will be responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian cells.

The appointed candidate will be responsible in the purification of 50L to 2000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents.

Essential Duties & Responsibilities

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis.
• Provides technical direction in the execution and development of the purification process.
• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products,...

We at Global Life Science Hub are recruiting on behalf of a leading biopharmaceutical company for a Downstream Manufacturing Scientist. This full-time role is ideal for a skilled professional with experience in downstream processing and purification techniques within a cGMP environment.

Position Summary:

The Downstream Manufacturing Scientist will be responsible for executing and optimizing purification processes to support the production of therapeutic proteins. You will work with a team to manage various stages of downstream processing, from capture through to final purification, ensuring high product quality and compliance with regulatory standards.

Key Responsibilities:

• Execute and optimize downstream processes, including chromatography, filtration, and other purification techniques.
• Collaborate with upstream teams to ensure seamless integration and transition of processes.
• Operate and troubleshoot downstream equipment,...

The Downstream Manufacturing Scientist is a hands-on position responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible in the purification of 50L to 1000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents.

Work in a team environment to execute batches and can work independently with minimum supervision. This position requires extensive technical expertise in mammalian cell-based purification processes, cGMP manufacturing and compliance for BLA requirements.

Essential Duties & Responsibilities

• Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting...