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Downstream Manufacturing Associate

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
New Jersey (USA), United States

Offer summary

Qualifications:

BSc or MSc in life science, Minimum 3 years' downstream processing experience, Experience in an Aseptic Manufacturing environment, Running Chromatography systems and packing columns, Familiarity with AKTA process skids.

Key responsabilities:

  • Perform downstream process in a cGMP environment
  • Provide technical direction for purification processes
  • Ensure timely execution of batches
  • Coordinate troubleshooting and data analysis
  • Comply with GMP and safety policies
Global Life Science Hub logo
Global Life Science Hub Human Resources, Staffing & Recruiting TPE https://glshub.com/
2 - 10 Employees
See more Global Life Science Hub offers

Job description

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Your missions

Global Life Science Hub is partnered with an incredible biopharmaceutical company specializing in difficult-to-formulate biologics. Recently, the company has achieved 2 FDA approvals and is transitioning from R&D to a full-scale commercial organization looking to build a new state-of-the-art facility in New Jersey as they ramp up production efforts from 50L to 2000L in Q4.

To support further expansion, we seek an on-site Downstream Manufacturing Associate in New Jersey who will be responsible for purifying clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF, knowledge of initiating batch records, and experience packing chromatography columns.

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

Experience/Qualifications:

  • A BSc or MSc in a life science sector
  • A minimum of 3 years’ experience in downstream processing
  • Previous experience within in an Aseptic Manufacturing environment
  • Experience running Chromatography systems and packing columns
  • Ability to run TFF operations
  • Experience working with AKTA process skids and knowledge of unicorn software is highly desirable
  • 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 CDMO 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 – www.glshub.com

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
Check out the description to know which languages are mandatory.

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