Process Engineer in Holly Springs

Energy Jobline ZR; Holly Springs (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. is seeking an experienced Process Engineer to deliver technical support in a GMP pharma/biotech environment. You will drive process improvements, troubleshoot equipment, and coordinate cross-functional projects from problem identification through implementation.

The ideal candidate has 5+ years in pharmaceutical manufacturing, strong problem-solving and documentation skills, and a hands-on approach to continuous improvement.

Qualifications

• Bachelor’s degree in Chemical/Mechanical/Industrial/Bioengineering or related field.
• 5+ years of process/manufacturing engineering experience in pharma/biotech.
• Strong knowledge of GMP, change control, CAPA, and engineering documentation practices.

Responsibilities

• Provide day-to-day process engineering support to manufacturing and engineering operations.
• Evaluate process performance and identify opportunities to improve reliability, efficiency, capacity, quality.
• Lead or support troubleshooting and root-cause investigations related to manufacturing processes, equipment, and systems.
• Develop and implement engineering solutions to address process and equipment issues.
• Support capital projects, equipment upgrades, system modifications, and process improvement initiatives.

Skills

Problem solving

Technical writing

Cross-functional collaboration

GMP knowledge

Education

Bachelor’s degree in Chemical/Mechanical/Industrial/Bioengineering

Job description

Job DescriptionJob Description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking an experienced Process Engineer to provide technical engineering support within a regulated pharmaceutical/biotechnology manufacturing environment. The Process Engineer will work closely with Engineering, Manufacturing, Quality, Validation, Maintenance, and other cross-functional teams to support process performance, equipment and system improvements, troubleshooting, capital projects, and continuous improvement initiatives. The ideal candidate is a hands‑on engineer with strong technical problem‑solving skills, experience working in GMP‑regulated manufacturing environments, and the ability to independently manage engineering activities from problem identification through implementation and closure.

Description:

• Provide day-to‑day process engineering support to manufacturing and engineering operations.
• Evaluate process performance and identify opportunities to improve reliability, efficiency, capacity, quality, and operational performance.
• Lead or support troubleshooting and root‑cause investigations related to manufacturing processes, equipment, and systems.
• Develop and implement engineering solutions to address process and equipment issues.
• Support capital projects, equipment upgrades, system modifications, and process improvement initiatives.
• Develop and review technical documentation including engineering assessments, specifications, protocols, reports, procedures, and change‑control documentation.
• Support equipment and process design reviews, technical evaluations, and implementation activities.
• Coordinate engineering activities with Manufacturing, Quality, Validation, Automation, Maintenance, and other technical groups.
• Support commissioning, qualification, validation, startup, and turnover activities as required.
• Participate in change controls, deviations, investigations, CAPAs, and risk assessments from an engineering perspective.
• Analyze process and equipment data to identify trends, recurring issues, and improvement opportunities.
• Provide technical recommendations and support the development of corrective and preventive solutions.
• Coordinate activities with vendors, contractors, and equipment suppliers when required.
• Ensure engineering activities are performed in accordance with applicable GMP requirements, engineering standards, procedures, and safety expectations.
• Maintain clear documentation and communicate project status, technical issues, risks, and recommendations to stakeholders.
• Support continuous improvement and standardization initiatives within the Engineering organization.

Qualifications:

• Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, Bioengineering, or a related engineering discipline.
• Relevant process engineering experience within the pharmaceutical, biotechnology, medical device, or regulated manufacturing industry.
• Strong understanding of manufacturing processes, equipment, utilities, and engineering principles.
• Experience troubleshooting process and equipment‑related issues in a manufacturing environment.
• Knowledge of GMP requirements, change control, deviations, CAPA, and engineering documentation practices.
• Experience supporting equipment modifications, process improvements, or capital projects.
• Ability to analyze technical data and translate findings into practical engineering solutions.
• Strong technical writing, documentation, and communication skills.
• Demonstrated ability to work independently while collaborating effectively with multidisciplinary teams.
• Strong organizational skills with the ability to manage multiple activities and priorities.
• 5+ years of relevant process or manufacturing engineering experience within the pharmaceutical or biotechnology industry.
• Experience supporting biopharmaceutical manufacturing processes and equipment.
• Experience with commissioning, qualification, validation, and equipment startup.
• Familiarity with process optimization, process characterization, troubleshooting methodologies, and root‑cause analysis.
• Experience supporting capital projects and equipment/system lifecycle activities.
• Working knowledge of automation and process control systems.
• Experience working in a highly regulated GMP manufacturing environment.

Key Competencies: Process Engineering | Manufacturing Support | Troubleshooting | Root Cause Analysis | Process Optimization | Equipment & Systems | Technical Documentation | Change Control | CAPA | GMP Compliance | Capital Projects | CQV Support | Cross-Functional Collaboration | Continuous Improvement

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to , , , , , , , veteran status, or status.