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Pharma Process Engineer Jobs in Georgia (NOW HIRING)

Corporate Tax Manager | Atlanta, GA

Atlanta, GA · Hybrid

$110K - $148K/yr

Build and maintain strong client relationships by understanding operations, processes, and business ... pharma, food & beverage, consulting, engineering, telecommunications, or transportation ...

We are a young and innovative software company looking to dramatically change how pharma, biotech ... processes. Role Overview As a Customer Support Team Lead, you will manage the day-to-day operations ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

We ethically connect HCPs to pharma resources, reduce go-to-market costs and accelerate patient ... Partner closely with Product, Engineering, Legal, Operations, Finance, Concierge, and other ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... Experience with AI governance processes, including AI use case tracking, model risk classification ...

Showing results 41-60

Pharma Process Engineer information

See Georgia salary details

$41.8K

$77.7K

$120.3K

How much do pharma process engineer jobs pay per year?

As of Aug 9, 2026, the average yearly pay for pharma process engineer in Georgia is $77,698.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,900.00 and $87,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Pharma Process Engineers when optimizing manufacturing processes?

Pharma Process Engineers often encounter challenges such as maintaining strict regulatory compliance while implementing process improvements and ensuring product quality. Balancing efficiency with adherence to Good Manufacturing Practices (GMP) can be complex, especially during scale-up or technology transfer projects. Additionally, collaborating across multidisciplinary teams—including quality assurance, production, and R&D—requires strong communication skills to align objectives and resolve issues quickly. These challenges make adaptability and attention to detail crucial traits for success in the role.

What does a Pharma Process Engineer do?

A Pharma Process Engineer designs, develops, and optimizes manufacturing processes for pharmaceutical products. They ensure that production processes are efficient, safe, and compliant with regulatory standards like Good Manufacturing Practice (GMP). Their work often involves troubleshooting equipment, scaling up production from laboratory to industrial scale, and implementing process improvements to increase yield and product quality. They also collaborate closely with quality assurance and research teams to ensure that all products meet strict safety and efficacy standards.

What is the difference between Pharma Process Engineer vs Chemical Process Engineer?

AspectPharma Process EngineerChemical Process Engineer
Required CredentialsBachelor's in Chemical, Pharmaceutical, or related field; GMP certification often preferredBachelor's in Chemical Engineering or related field; Professional Engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, cleanroomsChemical plants, refineries, manufacturing sites
Industry UsagePharmaceutical, biotech, healthcareChemical, petrochemical, manufacturing
Common Search/ComparisonYesYes

Both Pharma Process Engineers and Chemical Process Engineers work in manufacturing environments requiring chemical engineering knowledge. Pharma Process Engineers focus on pharmaceutical production, adhering to strict GMP standards, while Chemical Process Engineers work across various chemical industries. Their roles overlap in process design and optimization, but Pharma Process Engineers specialize in drug manufacturing processes.

What are the key skills and qualifications needed to thrive as a Pharma Process Engineer?

To thrive as a Pharma Process Engineer, you need a strong background in chemical engineering or pharmaceutical sciences, often supported by a relevant degree and industry experience. Familiarity with process simulation software (such as Aspen Plus), GMP regulations, and validation protocols is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills set standout professionals apart in this field. These skills and qualities are important because they ensure safe, efficient, and compliant pharmaceutical manufacturing processes.
Infographic showing various Pharma Process Engineer job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $77,698 per year, or $37.4 per hour.

Principal Automation Engineer - Warehouse Automation (Holly Springs)

Genentech

Holly Springs, GA • On-site

Full-time

Re-posted 20 days ago


Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

Principal Automation Engineer - Warehouse Automation (Holly Springs)

Welcome to Holly Springs, North Carolina- home to Roche/Genentech's largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and Operational Excellence converge to create the global standard for high-volume, highly-efficient Drug Product manufacturing.

The facility's core is defined by Innovation - leveraging advanced automation, robotics, digital tools, real-time data analytics, and simple, streamlined processes to produce the highest quality medicines. This plant meets today's demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines and is scalable to grow with the portfolio, which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes. This is a fast-paced, entrepreneurial environment with a high-level of accountability, with planned launch in 2028.

The Opportunity

ITOT supports Pharma Technical Manufacturing (PTM), PTM is responsible for managing all aspects of end-to-end drug substance and drug product manufacturing and supply. From the raw material to the final medicine, we contribute to deliver Roche's ground-breaking therapies to more than 120 million patients around the world. We make our medicines at 9 sites around the world and coordinate all aspects of production of Roche medicines in all disease areas and dosage forms. To ensure readiness for a step-change in the standard of care that Roche delivers in the area of Cardiovascular, Renal and Metabolism (CVRM), PTM will construct a new manufacturing site in the U.S. in Holly Spring, North Carolina. ITOT will own and operate Manufacturing Technology stack at the site working with Global IT. The new site will focus on large volume low-cost Drug Product manufacturing (Component Prep & Compounding, Liquid PFS Filling, Automated Inspection, Autoinjector Assembly, Packaging/Finished Products).

Principal Automation Engineer is being hired to participate in Greenfield Project execution and then support the facility after going live.

Initially, you will perform a mix of remote and onsite work (first at the General Planner's office, later at construction site/plant). You will transition to local full-time on-site work once the site buildings are built and equipment delivered. Travel of up to 30% of the time is expected during the project phase.

The Principal Automation Engineer - Warehouse Automation is responsible for the technical integrity, reliability, and optimization of the automated material handling systems within the Holly Springs facility. This role serves as the subject matter expert for the Korber K.One.X (Warehouse Control System), high-density Automated Storage and Retrieval System (AS/RS systems), and the Automated Guided Vehicle (AGV) fleet. You will bridge the gap between physical hardware and the digital warehouse layer, ensuring that pharmaceutical stock moves seamlessly and safely through the production lifecycle while maintaining strict GxP compliance. The role will also have responsibilities for Robotics Fleet management System that may be shared with Site Robotics Engineer. Leading automation impacting projects with large and/or complex scope and Driving strategic initiatives to improve business processes are also expected.

Key Responsibilities:

Operational System Maintenance (AS/RS & WCS)

  • System Health Monitoring: Monitor the daily performance of the Korber K.One.X (WCS) and AS/RS, proactively identifying "stuck" telegrams or queue bottlenecks before they impact production output.

  • L2/L3 Technical Support: Act as the highest internal escalation point for complex automation failures. Troubleshoot the handshake between PLC layers and the WCS to resolve hardware-software "mismatches" in real-time.

  • Disaster Recovery: Maintain and periodically test the system recovery procedures for the WCS and PLC configurations to ensure rapid restoration of the warehouse flow in the event of a server or network failure.

AGV Fleet & Traffic Management

  • Fleet Availability: Manage the daily operational readiness of the AGV fleet, overseeing battery health, charging station rotations, and sensor calibration to ensure 99%+ fleet availability.

  • Dynamic Traffic Tuning: Adjust FMS (Fleet Management System) parameters (e.g., zone blocking, speed limits, or path priorities) based on shifting daily operational volumes to prevent congestion in high-traffic corridors.

  • Safety Integrity: Conduct routine operational audits of AGV safety fields and emergency stop circuits to ensure the equipment continues to operate within its validated safety envelope.

  • Manage Site Robotics Fleet Management Systems in partnership with future Robotics functions at the site.

IT/OT Bridge & Data Integrity

  • Interface Oversight: Monitor the SAP EWM-to-WCS (Black Box) message logs (IDocs/Web Services), resolving data discrepancies to ensure that the physical location of pharmaceutical stock always matches its digital twin in SAP.

  • Audit Trail Compliance: Ensure that all automated logs and event data required by 21 CFR Part 11 are accurately captured, archived, and available for regulatory inspections or quality audits.

  • Continuous Optimization: Analyze OEE (Overall Equipment Effectiveness) data from the WCS and AGV systems to propose small-scale logic adjustments that improve cycle times and reduce mechanical wear and tear.

Who You Are

  • Bachelor's degree in Chemical, Mechanical, Electrical, or Computer Science or a related discipline and 8 years of applicable automation and/or instrument and control system experience preferably majority in drug product function. Or, Master's degree in Engineering or a related discipline and 6 years of applicable automation and/or instrument and control system experience preferably majority in drug product function.

  • 5 years in the pharmaceutical/biotech industry/GMP experience is highly preferred.

  • 24X7 on call support, participate in an on-call environment to meet business continuity requirements, including weekends and holidays as required.

Technical Skills:

  • Proficiency in troubleshooting PLCs (Siemens TIA Portal or Rockwell Automation) and their communication protocols (Profinet/EtherNet/IP).

  • Strong understanding of SAP EWM or similar WMS interfaces (IDocs, queues, and RFC calls).

  • Familiarity with AGV navigation technologies (Laser, Natural, or Magnetic) and FMS software.

  • Knowledge of GAMP5 standards and 21 CFR Part 11 requirements is highly preferred.

Soft Skills:

  • Analytical mindset with the ability to perform root-cause analysis under production pressure.

  • Excellent communication skills to translate complex technical issues for cross-functional stakeholders in Logistics and Quality.

Physical Requirements:

  • Ability to work in a high-density warehouse environment, which may include working at heights or in proximity to moving automated machinery.

  • On-call support for 24/7 warehouse operations.

The expected salary range for this position based on the primary location of Holly Springs, North Carolina is $95,200 - $176,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

Relocation benefits are not available for this job posting.

#CVRM

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.


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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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