Find Manufacturing Associate Dsp Job in Princeton, New Jersey | Snaprecruit

Find Manufacturing Associate Jobs in Princeton
image
  • Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,
loadingbar
Loading, Please wait..!!

Manufacturing Associate Dsp

  • ... Posted on: Sep 10, 2024
  • ... Global Life Science Hub
  • ... Princeton, New Jersey
  • ... Salary: Not Available
  • ... Full-time

Manufacturing Associate Dsp   

Job Title :

Manufacturing Associate Dsp

Job Type :

Full-time

Job Location :

Princeton New Jersey United States

Remote :

No

Jobcon Logo Job Description :

Global Life Science Hub are seeking a Downstream Manufacturing Associate 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, instruments or equipment.
  • Ensure that engineering and clinical batches are executed in a timely manner.
  • Establishes operating equipment specifications and improves manufacturing techniques.
  • Works with other teams and outside vendors to resolve technical issues as well as maintenance of production equipment.
  • Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies.
  • Coordinate the conduction of investigations and corrections for issues found during the batch execution process.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

  • Requires a Bachelor or Master’ degree in chemical, biological or biochemical sciences and a minimum of 4- 5 years of related experience in the biopharmaceutical industry.
  • Previous experience working in GMP and aseptic manufacturing environment.
  • Experience working with AKTA Process skids or similar and familiarity of single use manufacturing consumables such as bags, tube sets, columns and process manifolds.
  • Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation.

Apply

Global Life Science Hub is a specialized Life Science headhunting firm. We place professionals across Europe and the US for various Biotechnology, Pharmaceutical, and CRO companies, ranging from small start-ups to large global organizations.

If you’re interested, please apply below. If this position doesn’t suit you, visit our website for more vacancies –

Jobcon Logo Position Details

Posted:

Sep 10, 2024

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-WOR-f78bf91352cb5f55d8625c053e49d65f8ede7efbfa790fbf71b515032d5e5d9d

City:

Princeton

Job Origin:

WORKABLE_ORGANIC_FEED

Share this job:

  • linkedin

Similar Jobs

Manufacturing Associate Dsp    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Global Life Science Hub are seeking a Downstream Manufacturing Associate 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, instruments or equipment.
  • Ensure that engineering and clinical batches are executed in a timely manner.
  • Establishes operating equipment specifications and improves manufacturing techniques.
  • Works with other teams and outside vendors to resolve technical issues as well as maintenance of production equipment.
  • Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies.
  • Coordinate the conduction of investigations and corrections for issues found during the batch execution process.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

  • Requires a Bachelor or Master’ degree in chemical, biological or biochemical sciences and a minimum of 4- 5 years of related experience in the biopharmaceutical industry.
  • Previous experience working in GMP and aseptic manufacturing environment.
  • Experience working with AKTA Process skids or similar and familiarity of single use manufacturing consumables such as bags, tube sets, columns and process manifolds.
  • Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation.

Apply

Global Life Science Hub is a specialized Life Science headhunting firm. We place professionals across Europe and the US for various Biotechnology, Pharmaceutical, and CRO companies, ranging from small start-ups to large global organizations.

If you’re interested, please apply below. If this position doesn’t suit you, visit our website for more vacancies –

Loading
Please wait..!!