Biopharma Downstream Operator - cGMP/Validation (Day Shift)

Scorpion Therapeutics; North Carolina; On-site; USD 70,000 - 100,000; Full time

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

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.