# Process Engineer

**Company**: GSK
**Experience**: senior
**Job type**: full-time
**Category**: Engineering
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Marietta/Sr-Process-Engineer_449687?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_fa09c92a-18e

## Description

Join a team dedicated to advancing the manufacturing of drug substances that improve lives. As a Process Engineer, you will develop and optimize processes to make medicines safely and efficiently. You will collaborate closely with cross-functional partners who share a commitment to science, quality, and continuous improvement.

**Responsibilities:**

- Lead the design, specification, procurement, installation, commissioning, validation, and continued technical support of bioprocess equipment and facility design / operation

- Facilitate multi-disciplined teams in the performance of HAZOPs, FMEAs, process reviews and SOP development efforts

- Act as a primary interface with outside engineering consulting firms on process design projects

- Manage vendors, consultants and contractors to ensure that process and project design and installation are in compliance with cGMP requirements & GSK Bio standards

- Stay current with technical developments in the field of vaccine formulation and manufacturing equipment design, equipment, control technology and GSK-Bio Standards

- Ensure all validation, quality, engineering, safety, and environmental procedures and regulations are met, maintained and documented appropriately

**Basic Qualifications:**

- Bachelor’s degree in engineering for a scientific field

- Minimum of 5 + years of experience in process engineering within pharmaceutical or medical device manufacturing

- Experience with Good Manufacturing Practices, Pharma or Vaccine formulation and filling facilities

- Technical understanding of the pharmaceutical industry and engineering practices

**Preferred Qualifications:**

- Demonstrated self-direct work habits along with verbal and written communication skills

- Familiarity with regulatory expectations regarding electronic records and electronic signatures

- Experience with process flow design and process optimization techniques

- Proven skills in documentation for compliance and regulatory audits

## Skills

### Required
- Asset Life Cycle Management
- Data Integrity
- Digital Fluency
- GxP Regulations
- Lean Management
- Manufacturing Technologies
- Pharmaceutical Manufacturing
- Problem Solving
- Risk Awareness
- Standards Compliance

### Nice to have
- Spanish

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