Global Life Science Hub
Global Life Science Hub is hiring: Downstream Manufacturing Scientist in Piscata
Global Life Science Hub, Piscataway, NJ, United States
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:
This role is an exciting opportunity for a professional with a strong background in downstream manufacturing to contribute to cutting-edge biopharmaceutical production. If you are ready to bring your expertise to a dynamic and innovative environment, we encourage you to apply.
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, ensuring efficient and compliant production runs.
- Document and review batch records, protocols, and other related technical documents.
- Implement process improvements to enhance yield, efficiency, and product quality.
- Ensure compliance with cGMP and safety regulations throughout the manufacturing process.
- Perform other assigned duties as required, contributing to overall process development and scale-up.
- Bachelor's or Master's degree in chemical, biological, or biochemical sciences with a minimum of 3+ years of relevant experience in the biopharmaceutical industry.
- Extensive experience in downstream processing, including chromatography and filtration techniques.
- Strong knowledge of cGMP regulations and experience working in a compliant manufacturing environment.
- Ability to work collaboratively in a team and independently with minimal supervision.
- Excellent communication, documentation, and problem-solving skills.
This role is an exciting opportunity for a professional with a strong background in downstream manufacturing to contribute to cutting-edge biopharmaceutical production. If you are ready to bring your expertise to a dynamic and innovative environment, we encourage you to apply.