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Manufacturing Supervisor (Third Shift) - Relocation Support Available

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor or Master's degree in chemical, biological or biochemical sciences, 7-10 years of related experience in biopharmaceutical industry, Experience in GMP and aseptic manufacturing environment, Familiarity with AKTA Process skids and single-use consumables, Knowledge of GMP documentation and processes.

Key responsabilities:

  • Lead and supervise downstream purification processes in a cGMP environment
  • Provide technical direction for purification process development
  • Evaluate operating data and adjust processes accordingly
  • Prepare and review quality management documents
  • Coordinate investigations and corrections during batch execution
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

Global Life Science Hub are searching for a Downstream Manufacturing Supervisor who will be responsible for leading and growing the team while executing purification on a wide range of mammalian based biologics. The ideal candidate should posses technical expertise with various chromatography methods.

Position summary: Location: The City of Chicago. Shift: Monday to Friday - 10pm - 6am. Salary: $40-$45p/h 1.5x over 40 hours.

Relocation: $5,000 relocation assistance is available for non-local candidates.

Responsibilities:

  • Perform and supervise 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.
  • Prepare/ review all quality management related documents (Deviation / Change control / investigation reports etc.)
  • 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 7 - 10 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:

The Global Life Science Hub are a niche Life Science headhunting firm. We place professionals across Europe and the US for a variety of Biotechnology, Pharmaceutical and CRO companies ranging from small start-ups to large global organisations.

If you’re interested, please apply below. If this position doesn’t interest you, please visit our website for a list of more vacancies – www.glshub.com

Required profile

Experience

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

Other Skills

  • Team Leadership

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