Manufacturing Associate IV / V, Small Scale Purification (Days)

Scorpion Therapeutics

North Carolina

On-site

USD 70,000 - 100,000

Full time

10 days ago
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Benefits offered by this job

Training and safety emphasis

Job summary

Scorpion Therapeutics is hiring a Manufacturing Associate for biopharma drug substance production, focusing on downstream purification like chromatography, viral filtration, and ultrafiltration. You will operate process equipment and follow strict cGMP guidelines.

Day shift (6 AM–6 PM ET) on a 2-2-3 rotation, with emphasis on training, safety, and seamless production in a fast-paced, 24/7 RTP facility.

Qualifications

  • Bachelor's degree (STEM preferred) or equivalent experience
  • Prior cGMP environment experience
  • Familiarity with aseptic/cleanroom conditions
  • Understanding of process automation systems

Responsibilities

  • Operate process equipment
  • Follow SOPs
  • Perform in-process sampling
  • Document deviations
  • Support validation activities

Skills

Aseptic/cleanroom understanding
Process automation knowledge
Documentation accuracy

Education

Bachelor's degree (STEM) or equivalent experience

Tools

Pipetting
Single-use consumables exposure

Job description

Role

Manufacturing Associate in biopharma drug substance production, focusing on downstream purification processes such as chromatography, viral filtration, and ultra-filtration.

Objectives

Execute daily cGMP manufacturing activities, ensure documentation accuracy, and maintain environment readiness.

Responsibilities
  • Operate process equipment
  • Follow SOPs
  • Perform in-process sampling
  • Document deviations
  • Support validation activities
Requirements
  • Bachelor's degree (STEM preferred) or equivalent experience (2-5 years)
  • Prior cGMP environment experience
  • Familiarity with aseptic/cleanroom conditions
  • Understanding of process automation systems
Preferred
  • Pipetting experience
  • Exposure to single-use consumables
High-Value
  • Biologics manufacturing
  • Downstream process steps
  • cGMP compliance
  • Validation support in a 24/7 RTP facility
Work setup

Day shift (6 AM-6 PM ET) on a 2-2-3 rotation; collaborative environment emphasizing training and safety.

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