Process Engineer II

Scorpion Therapeutics; Boston (MA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics in Somerville, MA, is seeking a Process Engineer II to support cGMP manufacturing of autologous cell therapies within the MSAT team. You will focus on technology transfer, process support, and ongoing commercial production.

The role requires a Bachelor’s or Master’s in Engineering or Life Sciences with 3–5 years in biopharma manufacturing, MSAT, or CMC. Strong communication and leadership skills are essential, with familiarity in regulatory standards.

Qualifications

• Experience in biopharma manufacturing within MSAT/CMC is preferred.
• Strong knowledge of manufacturing processes and project management.
• Excellent communication and leadership skills.

Responsibilities

• Lead technical support for GMP runs.
• Conduct investigations using root cause analysis.
• Develop process trending and verification programs.
• Drive continuous improvement projects.
• Coordinate cross-functional tech transfer teams.
• Prepare and review technical documentation.
• Oversee engineering and process qualification runs.

Skills

Biopharma manufacturing experience

MSAT/CMC experience

Root cause analysis

Education

Bachelor’s or Master’s in Engineering, Life Sciences, or related field

Job description

Role:

Process Engineer II supporting cGMP manufacturing of autologous cell therapies within the MSAT team, focusing on technology transfer, process support, and ongoing commercial production.

Responsibilities:

lead technical support for GMP runs, conduct investigations using root cause analysis, develop process trending and verification programs, drive continuous improvement projects, coordinate cross-functional tech transfer teams, prepare and review technical documentation, and oversee engineering and process qualification runs.

Requirements:

Bachelor’s or Master’s in Engineering, Life Sciences, or related field; 3-5 years in biopharma manufacturing, MSAT, or CMC, with experience in cell/gene therapy or biologics preferred; strong knowledge of manufacturing processes, root cause analysis, and project management; excellent communication and leadership skills; familiarity with regulatory standards and statistical tools.

HighValue:

autologous cell therapies, cGMP environment, tech transfer, process qualification, root cause analysis, process trending, biologics/cell/gene therapy experience.

WorkSetup:

hybrid Somerville, MA; no travel specified.