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Pharma Process Engineer Jobs in Georgia (NOW HIRING)

Manus Bio

Process Engineer

Augusta, GA · On-site

We are seeking a highly motivated Process Engineer to support manufacturing operations. This hands ... Experience in food or pharma industry desired Preferred Working Style: * Must be fully responsible ...

Manus Bio

Process Engineer

Augusta, GA

We are seeking a highly motivated Process Engineer to support manufacturing operations. This hands ... Experience in food or pharma industry desired Preferred Working Style: * Must be fully responsible ...

Global Pharma Tek

Sr. Analytics Developer

Atlanta, GA · On-site

Global Pharma Tek is seeking a Sr. Analytics Developer to design, develop, test, maintain, and ... business processes into BI reporting and analysis solutions. • Ability to follow the Software ...

Gerresheimer

Assembly Process Technician

Peachtree City, GA · On-site

$16.25 - $20.50/hr

... pharma and biotech industry. www.gerresheimer.com Join Gerresheimer in Peachtree City, GA as a ... Associate or Bachelor's in Engineering preferred * 2+ years in manufacturing or technical training;

Gerresheimer

Assembly Process Technician

Peachtree City, GA

$16.25 - $20.50/hr

... pharma and biotech industry. www.gerresheimer.com Join Gerresheimer in Peachtree City, GA as a ... Associate or Bachelor's in Engineering preferred * 2+ years in manufacturing or technical training;

Aequor

Understands pharma grade utilities ( water HVAC, gases) Support Maintenance, Engineering and ... Skills Aseptic processing Protocol generation Sterilization Validation FDA/USDA Education:Bachelors ...

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All JobsPharma Process Engineer JobsPharma Process Engineer Jobs in Georgia

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 30, 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 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 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.

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 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 popular job titles related to Pharma Process Engineer jobs in Georgia?

For Pharma Process Engineer jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Pharma Process Engineer jobs in Georgia look for?

The top searched job categories for Pharma Process Engineer jobs in Georgia are:

Pharma Process Engineer jobs near you
Infographic showing various Pharma Process Engineer job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 15% Part Time, 7% Contract, and 3% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $77,698 per year, or $37.4 per hour.

Process Engineer

Augusta, GA • On-site

Manus Bio
Biotechnology Research and Development • 51 - 200 employees
Learn more about Manus Bioexternal

Full-time

Re-posted 14 days ago

Job description

Manus works across industries and value chains to accelerate the transition to BioAlternatives � better performing and more sustainable versions of complex molecules traditionally sourced from plants, animals, or fossil fuels. Our platform is proven to work across scales, bridging the Valley of Death between lab and manufacturing more efficiently and more reliably to deliver the benefits of synthetic biology today.
We are seeking a highly motivated Process Engineer to support manufacturing operations. This hands-on position requires a desire and ability to work as an integral part of a multidisciplinary team, as well as the demonstration of a high degree of flexibility, creativity, and initiative applied to the various duties and aspects of the position. This person will be expected to play an integral part of the company's operations team.
Why work for the Company:
  • Opportunity � For motivated, results-oriented team members, our growth creates opportunities for personal and professional advancement.
  • Accountability � You are given the resources you need to succeed and the freedom to make it happen; in return, we hold each other accountable for our high expectations.
  • Passion � We love what we do and enjoy working with others who feel the same way. We embrace the challenge and hard work that comes with working on the cutting edge.

Responsibilities:
Provides day-to-day process monitoring, including troubleshooting of process, yield, quality and equipment reliability issues.
  • Develops and maintains plant material balances, capacity evaluations, and area/plant yields. Reports on critical items through KPIs.
  • Scale up R&D equipment and processes to improve yields and cycle time on new processes.
  • Engage with product marketing and manufacturing groups for process requirements.
  • Collaborate with manufacturing to ensure equipment can be reliable and meet quality and cost targets. This activity includes design for enhancements to existing equipment manufacturability and new product equipment.
  • Identifies, develops and implements process capacity and efficiency (yield) improvements, including operator tracking and downtime data and leading technical improvement teams.
  • Develops and maintains area process sample schedules and provides coordination with lab.
  • Performs execution and documentation of plant trials including detailed material balances and evaluation of in-process quality and batch record data.
  • Monitors equipment performance and in-use time and coordinates production issues with the appropriate personnel.
  • Completes investigations and Corrective Action Reports for technical processing issues.
  • Initiates/supports area capital projects, including scope development, cost justification, control logic and start-up support. Take part in project teams as Leader, technical expert or operational expert.
  • Perform as equipment and/or technology owner or expert to support operation and train operators.
  • Provides Process Safety Management ownership responsibilities including process hazard analysis participation, supporting upkeep of drawings, procedures, and PSI files, and sponsoring management of change for equipment and process changes.
  • Supports site safety and quality initiatives through participation & leadership in teams, incident/CAR analysis, and follow-up.
  • Ensures smooth integration of activities and effective teamwork within Site Engineering functions (between project engineering, process engineering, and process controls engineering teams).

Required Qualifications:
  • B.S. in Chemical Engineering/Chemistry or a related discipline
  • Minimum three to eight years� experience in a chemical or pharmaceutical plant environment.
  • Knowledge of piping and valve operations to control processes.
  • Familiar with and capable of generating engineering flow diagrams, process flow diagrams, and capacity analysis.
  • Good understanding of analytical techniques (GC) and fermentation bioprocess is desirable.
  • Experience in food or pharma industry desired

Preferred Working Style:
  • Must be fully responsible and accountable for compliance with the provision of the safety, health, and environmental (SHE) policies
  • Must comply with Good Laboratory Practice and current Good Manufacturing Practice
  • Must be very well-organized and be able to handle multiple projects simultaneously
  • Must be a quick learner who is self-motivated and able to ask questions and seek clarity
  • Must be flexible with day-to-day duties and able to thrive in a start-up environment
  • Must be an excellent team member with strong communication skills and a desire to work collaboratively
  • Must hold him or herself to the highest professional, scientific and ethical standards

Apply