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Pharmaceutical Engineer Jobs in Florida (NOW HIRING)

5TH HQ

Bilingual Shipping Clerk

Hollywood, FL

$18/hr

Background in a regulated industry such as pharmaceuticals, engineering, or healthcare is a plus Key Responsibilities * Coordinate daily shipments with brokers and transportation providers to ensure ...

Crox Consulting Inc

Reliability Engineer

Boca Raton, FL · On-site

$100K - $125K/yr

Dear Candidate, We are currently hiring for the position of Reliability Engineer at a leading pharmaceutical manufacturing facility in Boca Raton, FL . This is a full-time opportunity with excellent ...

Unicon Pharma Inc.

Data Engineer

Davie, FL · On-site

$104K - $126K/yr

... in Pharmaceutical Industry. (The worker must have good understanding of the Pharmaceutical industry.) 6. Proficiency in programming languages such as Python, R, and SQL. Experience with machine ...

Crox Consulting Inc

Reliability Enginer

Boca Raton, FL · On-site

Experience in the pharmaceutical industry preferred. * Minimum 5 years of experience as reliability engineering/maintenance experience in cGMP, pharmaceutical/biological manufacturing environment ...

Germfree Laboratories Inc

Quality Engineer

Ormond Beach, FL · On-site

$63K - $81K/yr

Germfree engineers manufacture mission-critical controlled environments; modular and mobile cGMP cleanrooms, biosafety level (BSL-2 through BSL-4) biocontainment laboratories, pharmaceutical ...

Lonza

OT Engineer

Tampa, FL · On-site

OT Engineer Tampa, FL Today, Lonza is a global leader in life sciences operating across five ... Ensure OT systems remain reliable, secure, and compliant within a regulated pharmaceutical ...

Lonza

OT Engineer

Tampa, FL · On-site

OT Engineer Tampa, FL Today, Lonza is a global leader in life sciences operating across five ... Ensure OT systems remain reliable, secure, and compliant within a regulated pharmaceutical ...

Lonza

OT Engineer

Tampa, FL · On-site

OT Engineer Tampa, FL Today, Lonza is a global leader in life sciences operating across five ... Ensure OT systems remain reliable, secure, and compliant within a regulated pharmaceutical ...

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Pharmaceutical Engineer information

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How much do pharmaceutical engineer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for pharmaceutical engineer in Florida is $28.74, according to ZipRecruiter salary data. Most workers in this role earn between $27.31 and $30.19 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a pharmaceutical engineer, and why are they important?

To thrive as a Pharmaceutical Engineer, you need a strong background in chemical or biomedical engineering, pharmaceutical sciences, and process development, typically supported by a relevant bachelor's or master's degree. Familiarity with Good Manufacturing Practice (GMP) regulations, process simulation software, and quality assurance systems is essential. Exceptional problem-solving, attention to detail, and teamwork skills help you excel in cross-functional environments. These skills ensure safe, efficient drug production and regulatory compliance, which are vital for patient safety and business success.

What is the difference between Pharmaceutical Engineer vs Chemical Engineer?

AspectPharmaceutical EngineerChemical Engineer
CredentialsBachelor's in Pharmaceutical Engineering, Chemical Engineering, or related field; often requires industry-specific certificationsBachelor's in Chemical Engineering; professional engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, quality controlChemical plants, refineries, research labs
Industry UsagePrimarily in pharmaceutical and biotech industriesBroader industries including chemicals, energy, and materials
Job FocusDesigning and optimizing drug manufacturing processes, ensuring compliance with regulationsDesigning chemical processes, scaling up production, safety analysis

While both roles require a background in chemical processes, Pharmaceutical Engineers focus specifically on drug manufacturing and regulatory compliance within the pharmaceutical industry. Chemical Engineers have a broader scope, working across various chemical production sectors. The choice depends on your industry interest and specialization goals.

How do pharmaceutical engineers typically collaborate with cross-functional teams during drug development projects?

Pharmaceutical engineers work closely with scientists, quality assurance specialists, regulatory teams, and manufacturing staff throughout the drug development process. They play a key role in translating laboratory-scale processes into safe, efficient, and scalable manufacturing solutions. Effective communication and teamwork are crucial, as engineers must ensure that all technical, safety, and compliance requirements are met while balancing project timelines and budgets. This collaborative environment offers valuable opportunities to broaden your expertise and develop leadership skills, especially as you take on more responsibility in project management or process optimization roles.

What does a pharmaceutical engineer do?

Pharmaceutical engineers design and manufacture pharmaceutical products. As a pharmaceutical engineer, the focus of your work may be on chemical research, manufacturing design, field testing, quality assurance, packaging and labeling, product delivery, or regulations compliance. Your job duties include collaborating with other engineers and manufacturing personnel, and ensuring all procedures follow Good Manufacturing Practice Regulations established by the Food and Drug Administration (FDA). You need extensive science experience, strong analytical and problem-solving skills, and the ability to work well with a team.

More about Pharmaceutical Engineer jobs

What are the most commonly searched types of Pharmaceutical Engineer jobs in Florida?

The most popular types of Pharmaceutical Engineer jobs in Florida are:

What are popular job titles related to Pharmaceutical Engineer jobs in Florida?

For Pharmaceutical Engineer jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Engineer jobs in Florida look for?

The top searched job categories for Pharmaceutical Engineer jobs in Florida are:

What cities in Florida are hiring for Pharmaceutical Engineer jobs?

Cities in Florida with the most Pharmaceutical Engineer job openings:

What are popular job titles related to Pharmaceutical Engineer jobs in FL?

For Pharmaceutical Engineer jobs in FL, the most frequently searched job titles are:

Pharmaceutical Engineer jobs near you
Infographic showing various Pharmaceutical Engineer job openings in Florida as of July 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $59,783 per year, or $28.7 per hour.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Re-posted 3 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.

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