Senior Peptide Process Engineer—Scale-Up & Tech Transfer

AbbVie Inc.; Greenlawn (NY); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie Inc. in New York seeks a Peptide Process Engineer to lead research and development of scalable peptide manufacturing processes across lab, pilot plant, and manufacturing environments.

You will drive robust process steps for peptide modalities and support tech transfer to manufacturing with a focus on safety and quality. Independently lead projects, mentor scientific staff, and contribute to publications, regulatory documents, and patents while collaborating with quality, regulatory, and

Qualifications

• BS, MS, or PhD in chemical engineering or a related field; 12+ (BS), 10+ (MS), or 3+ (PhD) years of relevant industrial experience.
• Possesses excellent written and oral communication skills.
• Possess thorough theoretical and practical understanding of own scientific discipline.

Responsibilities

• Apply chemical engineering principles (kinetics, transport, thermodynamics, modeling) to experimental design and data analysis.
• Adhere to safety, GxP, and regulatory standards in all activities.
• Solve key project hurdles using scientific creativity and technical expertise.
• Maintain productive lab, pilot plant, and manufacturing support performance with minimal supervision.
• Publish, present, and/or document results; contribute to regulatory documents or patents.
• Serve as a subject matter expert on cross-functional teams and mentor others.
• Lead initiatives to improve operational efficiency and technology platforms.
• Mentor junior scientists to support technical and professional growth.

Skills

Communication skills

Strong scientific knowledge

Education

BS in Chemical Engineering

MS in Chemical Engineering

PhD in Chemical Engineering

Job description

AbbVie Inc. in New York seeks a Peptide Process Engineer to lead research and development of scalable peptide manufacturing processes across lab, pilot plant, and manufacturing environments.

You will drive robust process steps for peptide modalities and support tech transfer to manufacturing with a focus on safety and quality. Independently lead projects, mentor scientific staff, and contribute to publications, regulatory documents, and patents while collaborating with quality, regulatory, and