Downstream Manufacturing Associate

The role will involve performing downstream manufacturing to assure that the process is robust, scalable, and able to be performed in the manufacturing facility – as well as the accompanying documentation. The successful candidate will be familiar with cGMP regulations and technology transfer tasks and work out of the brand-new state-of-the-art facility in New Jersey, USA.

This position requires great attention to detail, ability to work in a team environment and a keen interest in optimisation of processes. Scientists will be responsible for adhering to all Quality Management System procedures, safety policies, and relevant parts of cGMP.

Responsibilities:

• Perform as a key member of the Downstream Manufacturing team, liaising with Process development and QA teams 
• Design and optimize downstream processing steps, including DNA purification techniques such chromatography, tangential flow filtration and formulation
• Wide...

The role will involve performing downstream manufacturing to assure that the process is robust, scalable, and able to be performed in the manufacturing facility – as well as the accompanying documentation. The successful candidate will be familiar with cGMP regulations and technology transfer tasks and work out of the brand-new state-of-the-art facility in New Jersey, USA.

This position requires great attention to detail, ability to work in a team environment and a keen interest in optimisation of processes. Scientists will be responsible for adhering to all Quality Management System procedures, safety policies, and relevant parts of cGMP.

Responsibilities:

• Perform as a key member of the Downstream Manufacturing team, liaising with Process development and QA teams 
• Design and optimize downstream processing steps, including DNA purification techniques such chromatography, tangential flow filtration and formulation
• Wide...

To fuel the next phase of expansion we are hiring 4 DSP Scientists. The appointed DSP scientists will run and pack chromatography columns and execute TFF processes for purifying volumes ranging from 50L to 2000L in a cGMP environment. A strong background in downstream processing is crucial for efficiently executing engineering, clinical, and commercial batches.

Downstream Manufacturing Scientist - Biologics

Location: On-site, USA - New Jersey

Type: Full-time

Responsibilities:

• Execute downstream processes at multiple scales in a cGMP environment, including chromatography column packing, TFF operations, and data analysis.
• Provide technical leadership in the development and execution of purification processes.
• Utilize software tools to collect and analyze operating data, making real-time adjustments to optimize product yield and equipment performance.
...

Downstream Manufacturing Specialist

Downstream Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation.

Essential Duties & Responsibilities

• Execute downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including column packing, troubleshooting, and data analysis.
• Provide technical leadership in the development and execution of downstream purification processes.
• Utilize software systems to collect, monitor, and evaluate operational data, making real-time adjustments to downstream processes,...

Downstream Manufacturing Specialist

Downstream Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation.

Essential Duties & Responsibilities

• Execute downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including column packing, troubleshooting, and data analysis.
• Provide technical leadership in the development and execution of downstream purification processes.
• Utilize software systems to collect, monitor, and evaluate operational data, making real-time adjustments to downstream processes,...