Senior Process Engineer - GMP & Validation Lead

Allergan; Branchburg Township (NJ); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) plan

Job summary

AbbVie is seeking a skilled Process Engineer to provide technical support to cross-functional teams, manage projects from concept to closure, and apply engineering expertise to manufacturing operations.

The role emphasizes process validation, equipment qualification, investigations, and collaboration across disciplines to drive manufacturing efficiency and product quality within a GMP environment.

Qualifications

• Bachelors degree in Engineering, Science, or related field or equivalent experience with 5+ years' engineering/operational work.
• Demonstrated competency in a technical discipline and ability to work with diverse teams.
• Strong technical knowledge and application of concepts, practices, and procedures.

Responsibilities

• Lead process engineering activities in the product line, including validation and investigations.
• Support and monitor Production to troubleshoot material, process and equipment issues.
• Provide technical evaluations for Engineering Change Orders and supplier changes.
• Design and develop equipment and processes for manufacturing products.
• Support integration of new products into manufacturing operations.
• Assist in validation of new/revised processes and equipment for compliance.
• Design and execute engineering studies to test hypotheses and outcomes.
• Apply scientific/technical knowledge to projects and supervise engineers or technicians if needed.

Skills

Process optimization

Cross-functional collaboration

Analytical reasoning

Problem solving

Communication

Education

Bachelor's degree in Engineering/Science

Tools

Data analysis tools

Job description

AbbVie is seeking a skilled Process Engineer to provide technical support to cross-functional teams, manage projects from concept to closure, and apply engineering expertise to manufacturing operations.

The role emphasizes process validation, equipment qualification, investigations, and collaboration across disciplines to drive manufacturing efficiency and product quality within a GMP environment.