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Pharmaceutical Process Engineer Jobs in Florida (NOW HIRING)

Reliability Engineer

Boca Raton, FL · On-site

$100K - $125K/yr

Minimum 5 years of experience in reliability or maintenance engineering, preferably in a cGMP pharmaceutical or biological manufacturing environment . * Hands-on experience with process equipment ...

Reliability Engineer

Boca Raton, FL

$95K - $119K/yr

Five to seven years of reliability engineering/maintenance experience preferably in a cGMP, pharmaceutical/biological manufacturing environment including experience with process equipment (pumps ...

... pharmaceutical, but if not, some type of chemical industry. 3. Bachelor's Degree Key ... engineering controls (e.g., ventilation, containment), administrative controls, and the selection ...

Senior Commissioning Agent

Tampa, FL · Hybrid

$93K - $134K/yr

Bachelor's Degree in Electrical or Mechanical Engineering or required years of experience, including commissioning of large distribution systems for industrial, datacenter, pharmaceutical processes ...

Senior Commissioning Agent

Tampa, FL · On-site

$93K - $134K/yr

Bachelor's Degree in Electrical or Mechanical Engineering or required years of experience, including commissioning of large distribution systems for industrial, datacenter, pharmaceutical processes ...

Data Engineer

Davie, FL · On-site

$104K - $126K/yr

... Pharmaceutical industry.) 6. Proficiency in programming languages such as Python, R, and SQL ... Analyze large datasets from manufacturing processes to derive actionable insights. b. Predictive ...

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

... in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments. * Basic understanding of manufacturing processes and engineering principles. * Familiarity with GMP/cGMP ...

Quality Engineer

Ormond Beach, FL · On-site

$63K - $81K/yr

... Labs, Pharmaceutical Isolators, Biosafety Cabinets, Modular & Mobile Controlled Environments ... Process and track nonconformances (NCMRs), corrective and preventive actions (CAPAs), and ...

Overview The Process Chemist is tasked with ensuring that our products meet the quality criteria of ... Civil Engineering or Laboratory field work (Chemical, Food, Pharmaceutical), is highly desirable.

Overview The Process Chemist is tasked with ensuring that our products meet the quality criteria of ... Civil Engineering or Laboratory field work (Chemical, Food, Pharmaceutical), is highly desirable.

Overview The Process Chemist is tasked with ensuring that our products meet the quality criteria of ... Civil Engineering or Laboratory field work (Chemical, Food, Pharmaceutical), is highly desirable.

Overview The Process Chemist is tasked with ensuring that our products meet the quality criteria of ... Civil Engineering or Laboratory field work (Chemical, Food, Pharmaceutical), is highly desirable.

About Actalent Actalent is a global leader in engineering and sciences services and talent ... We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing ...

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Pharmaceutical Process Engineer information

See Florida salary details

$22

$26

$29

How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 9, 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.
What are popular job titles related to Pharmaceutical Process Engineer jobs in Florida? For Pharmaceutical Process Engineer jobs in Florida, the most frequently searched job titles are:
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:
Infographic showing various Pharmaceutical Process Engineer job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $54,784 per year, or $26.3 per hour.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Re-posted 27 days ago


Job description

Position Summary

The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.

Essential Duties and Responsibilities

  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications

  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications

  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.