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Pharmaceutical Process Engineer Jobs in Florida (NOW HIRING)

Tech Tammina LLC

Process Engineer

Palm Beach, FL · On-site

Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals, Biological manufacturing environment. Must have the ability to apply engineering theory, practices ...

CEDENT

Process Engineer

Largo, FL · On-site

At least 5-10 years of process engineering/technical services/MS&T experience in the pharmaceutical/chemical manufacturing industry, preferably with cGMP manufacturing of FDA- regulated drug products.

Cedent

Process Engineer (Largo, FL)

Largo, FL · On-site

At least 5-10 years of process engineering/technical services/MS&T experience in the pharmaceutical/chemical manufacturing industry, preferably with cGMP manufacturing of FDA- regulated drug products.

CEDENT

Process Engineer (Largo, FL)

Largo, FL

Provide engineering services for full product life cycle including process robustness review ... Experience with pharmaceutical and consumer products related to creams, lotions, liquids, aerosols ...

Tech Tammina LLC

Sr. Process Engineers

Palm Beach, FL · On-site

$100K - $130K/yr

Position: Sr. Process Engineer Location: United States, , Palm Beach County Status: Full Time, ... Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals ...

Tech Tammina LLC

FL · On-site

$96K - $125K/yr

Position: Sr. Process Engineer Location: United States, , Palm Beach County Status: Full Time, ... Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals ...

Tech Tammina LLC

FL · On-site

$96K - $125K/yr

Position: Sr. Process Engineer Status: Full Time, Permanent Category: Engineering Location: Palm ... Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals ...

Tech Tammina LLC

FL · On-site

$96K - $125K/yr

Position: Sr. Process Engineer Location: United States, , Palm Beach County Status: Full Time, ... Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals ...

Nammo Defense System

Process Safety Engineer

Perry, FL · On-site

Experience in aerospace, defense, chemical processing, pharmaceutical manufacturing, specialty ... Professional Engineer (PE) license or Certified Process Safety Professional (CCPSC) certification ...

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Pharmaceutical Process Engineer information

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How much do pharmaceutical process engineer jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for pharmaceutical process engineer in Florida is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $24.81 and $27.84 per hour, depending on experience, location, and employer.

What is the difference between Pharmaceutical Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process EngineerPharmaceutical Manufacturing Technician
Required CredentialsBachelor's degree in engineering, chemistry, or related field; often includes certifications in process validationHigh school diploma or associate degree; on-the-job training or technical certifications
Work EnvironmentDesign, optimize, and oversee manufacturing processes in labs or production facilitiesOperate equipment, monitor production lines, and ensure quality in manufacturing settings
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturing organizationsPharmaceutical manufacturing plants, biotech production facilities

The main difference is that Pharmaceutical Process Engineers focus on designing and improving manufacturing processes, requiring higher technical credentials, while Pharmaceutical Manufacturing Technicians handle day-to-day production tasks and equipment operation. Both roles are essential in pharmaceutical production but differ in responsibilities and qualifications.

What Does a Pharmaceutical Process Engineer Do?

A pharmaceutical process engineer reviews the requirement to produce a pharmaceutical product and develops a process for manufacturing. In this career, your duties vary from employer to employer but usually include tasks such as providing technical specifications for machinery and equipment, working to estimate costs for production, and undertaking a negotiation for the procurement of necessary materials and ingredients. Your responsibilities as a process engineer may include providing analysis of the process to ensure efficiency, safety, and compliance with relevant regulations.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Process Engineer, and why are they important?

To thrive as a Pharmaceutical Process Engineer, you need a strong background in chemical or process engineering, pharmaceutical manufacturing, and regulatory compliance, typically supported by a relevant engineering degree. Familiarity with process simulation software (such as Aspen Plus), GMP standards, and quality management systems is essential. Attention to detail, problem-solving skills, and effective teamwork are crucial soft skills for optimizing processes and ensuring product quality. These competencies are vital for developing efficient, safe, and compliant pharmaceutical manufacturing processes that meet industry standards.

What are some common challenges faced by Pharmaceutical Process Engineers when scaling up production from laboratory to manufacturing scale?

Pharmaceutical Process Engineers often encounter challenges when translating lab-scale processes to full-scale manufacturing, such as maintaining product quality, ensuring process consistency, and meeting strict regulatory requirements. Controlling variables like temperature, pressure, and mixing at a larger scale can introduce unforeseen issues that require innovative problem-solving. Collaboration with cross-functional teams—including quality assurance, validation, and production staff—is essential to address these challenges efficiently. Adaptability and attention to detail are crucial in ensuring a smooth and compliant scale-up process.

What does a Pharmaceutical Process Engineer do?

A Pharmaceutical Process Engineer is responsible for designing, developing, and optimizing processes used in the manufacturing of pharmaceutical products. They ensure that production methods are efficient, safe, and compliant with regulatory standards. Their work involves troubleshooting process problems, implementing new technologies, and collaborating with other departments to improve product quality and production efficiency. They play a critical role in scaling up laboratory processes to full-scale manufacturing while maintaining product integrity and safety.
More about Pharmaceutical Process Engineer jobs
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What job categories do people searching Pharmaceutical Process Engineer jobs in Florida look for? The top searched job categories for Pharmaceutical Process Engineer jobs in Florida are:
What are popular job titles related to Pharmaceutical Process Engineer jobs in FL? For Pharmaceutical Process Engineer jobs in FL, the most frequently searched job titles are:
Pharmaceutical Process Engineer jobs near you
Infographic showing various Pharmaceutical Process Engineer job openings in Florida as of July 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $54,784 per year, or $26.3 per hour.

Process Engineer

GL Staffing Services, Inc.

Deerfield Beach, FL • On-site

$100K/yr

Full-time

Medical, Dental, Vision, PTO

Posted yesterday

New

Job description

We are seeking a highly analytical and solutions-driven Process Engineer to join our Deerfield area manufacturing facility. In this role, you will be the technical bridge between R&D, Quality, and Production. Your primary focus will be scaling up new formulations, optimizing current production runs, and troubleshooting complex manufacturing challenges on the floor.

The ideal candidate has a strong engineering background in the food, nutraceutical, or pharmaceutical industries, with a distinct preference for professionals who have direct experience in gummy production. If you excel at turning data into actionable process improvements and reducing manufacturing waste, we want you on our team.

Key Responsibilities

  • Process Optimization: Analyze and improve existing manufacturing processes for gummy production (including cooking, depositing, curing, and sanding) to increase yield, reduce cycle times, and minimize scrap.
  • Scale-Up & Commercialization: Partner closely with the R&D team to transition new gummy formulations from bench-top and pilot scale to full commercial production.
  • Troubleshooting & Root Cause Analysis: Lead investigations into process deviations (e.g., texture inconsistencies, setting failures, weight variations) using structured problem-solving methodologies to implement permanent corrective actions.
  • SOPs & Documentation: Develop, review, and update Standard Operating Procedures (SOPs), batch records, and process flow diagrams to ensure consistency and compliance across all shifts.
  • Equipment Integration: Collaborate with the Maintenance and Engineering teams to specify, install, and qualify new processing and packaging equipment.
  • Continuous Improvement: Utilize Lean Six Sigma principles to identify bottlenecks, conduct time studies, and execute cost-saving initiatives across the production floor.

Required Experience & Qualifications

  • Education: Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Food Engineering, Industrial Engineering, or a closely related technical field.
  • Industry Experience: 2 + years of hands-on process engineering experience within a continuous manufacturing environment (food, dietary supplements, or pharmaceuticals).
  • Gummy Expertise: Direct experience with gummy manufacturing processes (pectin, gelatin, starchless depositing systems, etc.) is highly preferred.
  • Technical Skills: Proficiency in statistical process control (SPC), Design of Experiments (DOE), and reading technical schematics (P&ID).
  • Regulatory Knowledge: Solid understanding of cGMP, FDA compliance, and food safety standards.
  • Communication: Exceptional ability to communicate technical concepts to non-technical staff, including machine operators and senior leadership.

Preferred Certifications

  • Lean Six Sigma Green Belt or Black Belt certification.
  • Project Management Professional (PMP) or equivalent training.

What We Offer

  • Competitive base salary of $100,000 / year.
  • Comprehensive benefits package (Health, Dental, Vision).
  • Paid time off and company holidays.
  • Opportunity to drive technical innovation in a fast-growing, highly specialized manufacturing sector.