Pharma Process Engineer (2nd Shift) - GMP & Process Improvement

UNAVAILABLE; East Windsor Township (NJ); On-site; USD 92,000 - 147,000; Full time

Benefits offered by this job

401(k)

Paid time off

Health coverage

Job summary

Hovione is seeking a Process Engineer for a 2nd shift (1:30pm–10:00pm) in New Jersey. You will design manufacturing processes, ensure cGMP compliance, and lead cross-functional activities to optimize production of drug substances and products.

You will prepare manufacturing documentation, conduct risk assessments, and drive CAPAs. Experience in pharmaceutical manufacturing and capital projects is essential; SAP and MS Office proficiency are preferred.

Qualifications

• Degree in Science or Engineering (Chem. Eng. preferred).
• Experience in pharmaceutical fine chemistry or related areas.
• GMP and HSE practices experience desired.

Responsibilities

• Plan and design manufacturing processes for intermediates and drug products.
• Prepare and review GMP documentation (batch records, validation plans/reports).
• Lead risk assessments and implement CAPAs.
• Support tech transfers and capital projects.
• Report KPIs and participate in audits and investigations.

Skills

GMP experience

HSE practices

Process engineering

Technical transfer

Capital project support

Education

Science or Engineering degree (Chemical Engineering preferred)

Tools

MS Office

SAP

Job description

Hovione is seeking a Process Engineer for a 2nd shift (1:30pm–10:00pm) in New Jersey. You will design manufacturing processes, ensure cGMP compliance, and lead cross-functional activities to optimize production of drug substances and products.

You will prepare manufacturing documentation, conduct risk assessments, and drive CAPAs. Experience in pharmaceutical manufacturing and capital projects is essential; SAP and MS Office proficiency are preferred.