MSAT Engineer II: Biologics Tech Transfer & Scale-Up

Energy Jobline ZR; Oklahoma City (OK); On-site; USD 110,000 - 160,000; Full time

Job summary

Energy Jobline ZR is seeking an MSAT Engineer II to support manufacturing as a technical advisor and drive technology transfer and process scale-up from R&D to manufacturing. The role covers mammalian upstream/downstream processes, BOMs, validation protocols, and process documentation.

You will collaborate with Facilities and Engineering to specify equipment needs, review process trends, and support manufacturing campaigns.

Qualifications

• PhD or MS in engineering or a relevant life-science field with a minimum of 3 years industry experience in GMP production.
• BS in engineering or relevant life-science related field with a minimum of 5 years industry experience in GMP Production.
• Experience in technical transfer and scale-up of biologics drug substance required; experience with single-use technologies.

Responsibilities

• Follow established policies, procedures, and strategies that are consistent with cGMP regulations for early and late-phase programs.
• Adhere to Quality standards and regulatory requirements.
• Possess proficiency in understanding scale-up requirements for mammalian cell culture and downstream purification.
• Advise internal and external development groups on manufacturing scale feasibility throughout process lifetime.
• Lead and participate in troubleshooting to improve operations.
• Coordinate with other departments to maintain process timelines.
• Other duties as assigned.

Skills

GMP production experience

Tech transfer

Scale-up knowledge

Regulatory knowledge

Written/oral/presentation skills

Leadership abilities

Problem solving

Collaboration skills

Flexible scheduling

Education

PhD or MS in engineering or a life-science field

BS in engineering or life-science field

Job description

Energy Jobline ZR is seeking an MSAT Engineer II to support manufacturing as a technical advisor and drive technology transfer and process scale-up from R&D to manufacturing. The role covers mammalian upstream/downstream processes, BOMs, validation protocols, and process documentation.

You will collaborate with Facilities and Engineering to specify equipment needs, review process trends, and support manufacturing campaigns.