Senior Bioconjugation & ADC Process Engineer

Lotte Biologics; City of Syracuse (NY); On-site; USD 91,000 - 142,000; Full time

Benefits offered by this job

Travel <5%

Job summary

LOTTE BIOLOGICS in East Syracuse, NY seeks a Senior Engineer, Bioconjugation Operations to lead bioconjugation and ADC manufacturing processes across development stages. You will drive technology transfer, scale‑up activities, and implement cGMP compliant improvements while mentoring junior engineers.

The role requires 7+ years in biopharmaceutical manufacturing with ADC/HPAPI experience and strong cross‑functional collaboration. On‑site position with <5% travel and a competitive NY pay range.

Qualifications

• Bachelor’s degree in Chemical Engineering, Chemistry, Biology or related field required.
• Advanced degree (MS/PhD) preferred.
• 7+ years of experience in biopharmaceutical manufacturing, process engineering, MSAT, technology transfer or manufacturing sciences is required.
• Experience with ADCs, bioconjugation processes, HPAPIs, or related complex manufacturing technologies is strongly preferred.

Responsibilities

• Lead technical SME for bioconjugation/ADC manufacturing processes across development stages.
• Lead technology transfer and scale‑up activities for bioconjugation and ADC processes.
• Provide technical leadership and mentoring to junior engineers and manufacturing personnel.
• Develop and maintain process descriptions, flow diagrams, and models; support audits and regulatory responses.

Skills

Bioconjugation

ADC manufacturing

Process engineering

Technology transfer

cGMP knowledge

Data analysis (DOE, JMP)

Cross-functional collaboration

Regulatory readiness

Education

Bachelor’s degree in Chemical Engineering, Chemistry, Biology or related field

Advanced degree preferred

Tools

JMP

Job description

LOTTE BIOLOGICS in East Syracuse, NY seeks a Senior Engineer, Bioconjugation Operations to lead bioconjugation and ADC manufacturing processes across development stages. You will drive technology transfer, scale‑up activities, and implement cGMP compliant improvements while mentoring junior engineers.

The role requires 7+ years in biopharmaceutical manufacturing with ADC/HPAPI experience and strong cross‑functional collaboration. On‑site position with <5% travel and a competitive NY pay range.