GMP Manufacturing Associate

Scorpion Therapeutics; Germantown (MD); On-site; USD 65,000 - 90,000; Full time

Job summary

Scorpion Therapeutics in Maryland is hiring a GMP Gene Manufacturing Associate I/II to produce clinical and commercial adenovector products in a cGMP setting. You will assemble raw materials, execute Master Batch Records, and support SOP development in a cross-functional team.

The ideal candidate holds a Bachelor's or Master's in biology or life sciences, with 1–3 years GMP manufacturing experience and aseptic technique expertise. Prior cell culture/purification and TFF familiarity are a plus.

Qualifications

• Bachelor's or Master's degree in biology, biomedical science, or life sciences.
• 1–3 years GMP manufacturing experience.
• Aseptic technique expertise.

Responsibilities

• Assembling raw materials.
• Executing Master Batch Records.
• Supporting SOP development.
• Managing deviations.
• Ensuring equipment cleanliness and changeovers.
• Participating in technology transfer and working within a cross-functional team while adhering to safety and regulatory standards.

Skills

aseptic technique

Education

Bachelor's or Master's in biology, biomedical science, or life sciences

Job description

Role: GMP Gene Manufacturing Associate I/II responsible for producing clinical and commercial adenovector products in a cGMP setting.

Core responsibilities

• assembling raw materials
• executing Master Batch Records
• supporting SOP development
• managing deviations
• ensuring equipment cleanliness and changeovers.

The role entails participation in technology transfer and working within a cross-functional team while adhering to safety and regulatory standards.

Requirements

• Bachelor's or Master's in biology, biomedical science, or life sciences
• 1-3 years GMP manufacturing experience
• aseptic technique expertise

Preferred

• prior cell culture/purification experience
• TFF familiarity

HighValue

• GMP manufacturing
• adenovector gene therapy products
• clinical and commercial phases
• cGMP compliance
• SOP development
• deviation management

Work setup: on-site with occasional weekend and shift work.