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Pharmaceutical Chemical Engineer Entry Level Jobs in Boca Raton, FL

... for pharmaceutical manufacturing equipment and facilities. This is a hands-on, entry-level role ... Collaborate cross-functionally with MS&T, QA, QC, Engineering, and Manufacturing teams. Education ...

... 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 ...

Bachelor's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Food Science, or related technical field * 1+ year of experience in product development, process development, scale-up ...

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Pharmaceutical Chemical Engineer Entry Level information

See Boca Raton, FL salary details

$38K

$83K

$132.9K

How much do pharmaceutical chemical engineer entry level jobs pay per year?

As of Aug 22, 2026, the average yearly pay for pharmaceutical chemical engineer entry level in Boca Raton, FL is $83,022.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,100.00 and $101,100.00 per year, depending on experience, location, and employer.

What does a pharmaceutical chemical engineer entry level do?

A Pharmaceutical Chemical Engineer Entry Level assists in designing, developing, and optimizing processes for manufacturing pharmaceutical products. They work with senior engineers and scientists to ensure production methods comply with safety and regulatory standards, often focusing on improving efficiency, quality, and cost-effectiveness. Their responsibilities may include conducting experiments, analyzing data, troubleshooting equipment, and preparing documentation for process validation. Entry-level engineers typically gain experience in Good Manufacturing Practices (GMP) and collaborate with cross-functional teams to support new drug development and scale-up activities.

What are some typical challenges faced by entry-level pharmaceutical chemical engineers during their first year on the job?

Entry-level pharmaceutical chemical engineers often encounter challenges such as adapting to strict regulatory standards, learning complex manufacturing processes, and quickly mastering specialized equipment. They may also need to develop strong communication skills to effectively collaborate with cross-functional teams including quality assurance, production, and research and development. Balancing multiple projects while ensuring adherence to Good Manufacturing Practices (GMP) can be demanding, but these experiences provide valuable learning opportunities and help build a solid foundation for career growth in the industry.

What are the key skills and qualifications needed to thrive as an entry-level pharmaceutical chemical engineer, and why are they important?

To thrive as an Entry-Level Pharmaceutical Chemical Engineer, you need a bachelor's degree in chemical engineering or a related field, along with a solid understanding of pharmaceutical manufacturing processes and regulations. Familiarity with process simulation software, GMP (Good Manufacturing Practice) standards, and laboratory instrumentation is typically required. Strong analytical thinking, attention to detail, and effective teamwork skills help you excel in cross-functional environments. These competencies are crucial to ensure product quality, regulatory compliance, and efficient process optimization in pharmaceutical production.

What is the difference between Pharmaceutical Chemical Engineer Entry Level vs Chemical Process Engineer?

AspectPharmaceutical Chemical Engineer Entry LevelChemical Process Engineer
Required CredentialsBachelor's in Chemical Engineering or related field; some roles may require internshipsBachelor's or higher in Chemical Engineering; professional certifications optional
Work EnvironmentPharmaceutical manufacturing facilities, laboratoriesChemical plants, manufacturing sites, industrial settings
Industry UsagePrimarily in pharmaceutical and biotech industriesBroader industrial sectors including chemicals, energy, and manufacturing

While both roles require a background in chemical engineering, Pharmaceutical Chemical Engineer Entry Level positions focus on drug manufacturing and quality control within the pharmaceutical industry. In contrast, Chemical Process Engineers work across various industries, designing and optimizing chemical processes in broader industrial settings.

What are popular job titles related to Pharmaceutical Chemical Engineer Entry Level jobs in Boca Raton, FL?

For Pharmaceutical Chemical Engineer Entry Level jobs in Boca Raton, FL, the most frequently searched job titles are:

What cities near Boca Raton, FL are hiring for Pharmaceutical Chemical Engineer Entry Level jobs?

Cities near Boca Raton, FL with the most Pharmaceutical Chemical Engineer Entry Level job openings:

$21/hr

Full-time

Re-posted 27 days ago


Job description

Job Summary:  

 
The Blender Operator I is responsible for performing pharmaceutical blending and compounding operations involving active pharmaceutical ingredients (APIs), potent compounds, adhesives, solvents, and other hazardous materials in a cGMP-regulated manufacturing environment. 

This position supports batch manufacturing activities through proper equipment setup, material dispensing, compounding operations, documentation, cleaning, and in-process monitoring activities. The role ensures manufacturing activities are performed safely, accurately, and in compliance with current Good Manufacturing Practices (cGMP), FDA, DEA, environmental health and safety requirements, and company procedures. 

The Blender Operator I is expected to demonstrate operational proficiency, strong documentation practices, teamwork, and consistent execution of manufacturing activities while supporting production schedules, product quality, and inspection readiness. 

 
 

Job Responsibilities 

Manufacturing & Compounding Operations 

  • Perform pharmaceutical blending and compounding activities in accordance with approved batch records and SOPs.  

  • Manufacture batches containing active pharmaceutical ingredients (APIs), potent compounds, adhesives, solvents, and other regulated or hazardous materials.  

  • Assemble, disassemble, operate, clean, and sanitize blending and compounding equipment, kettles, tanks, mixers, pumps, and associated manufacturing systems.  

  • Perform raw material dispensing, weighing, staging, and verification activities using calibrated equipment and approved procedures.  

  • Conduct batch record calculations and verify material quantities, yields, and reconciliation activities.  

  • Perform in-process checks, sampling, and coat weight verification activities as required.  

  • Monitor and document operational parameters including temperature, mixing speeds, vacuum, pressure, and processing times.  

  • Support manufacturing operations within production and other departments as needed. 

GMP Documentation & Compliance 

  • Accurately complete batch records, logbooks, equipment usage records, and all GMP documentation in accordance with Good Documentation Practices (GDP).  

  • Ensure all manufacturing activities comply with FDA, DEA, OSHA, cGMP, and company quality requirements.  

  • Maintain inspection-ready documentation and work areas at all times.  

  • Follow data integrity principles and ensure accurate, contemporaneous, and complete documentation practices.  

  • Comply with all company policies, safety procedures, and standard operating procedures while performing job duties. 

  • Operates in accordance with the company’s Code of Conduct, Business Ethics, and all established regulatory and compliance requirements. 

Equipment & Area Maintenance 

  • Perform cleaning and line clearance activities for manufacturing equipment and production suites. 

  • Maintain blending rooms, equipment storage areas, and manufacturing spaces in a clean, organized, and compliant condition. 

  • Identify and report equipment malfunctions, process abnormalities, or safety concerns promptly. 

  • Support preventive maintenance and calibration activities as required. 

Training & Team Support 

  • Work collaboratively with Manufacturing, Quality, Warehouse, Engineering, and EHS departments to support operational goals.  

  • Assist in training and supporting Blender Operator I personnel as directed.  

  • Participate in operational improvement and safety initiatives.  

  • Operates in accordance with the company’s Code of Conduct, Business Ethics, and all established regulatory and compliance requirements. 

Safety & Environmental Compliance 

  • Properly use required personal protective equipment (PPE), including respirators, coveralls, gloves, hearing protection, and eye protection. 

  • Safely handle potent compounds, solvents, and hazardous materials in accordance with established safety procedures. 

  • Follow all environmental health and safety procedures, including hazardous waste handling and spill response requirements. 

  • Participate in safety initiatives, risk assessments, and operational improvement activities. 

  • Perform all other duties as assigned.

Job Requirements 

Education 

  • High school diploma or General Education Degree (GED) required. 

  • Technical certification or vocational training in manufacturing, pharmaceutical operations, or related discipline preferred. 

Experience 

  • Minimum of 5 years of experience in pharmaceutical, chemical, food, or other regulated manufacturing environments required.  

  • Minimum of 3 years of experience as a Blender Operator I or equivalent pharmaceutical manufacturing experience preferred.  

  • Experience handling potent compounds or hazardous materials preferred.  

  • Demonstrated experience operating blending, mixing, coating, or compounding equipment preferred. 

Knowledge, Skills and Abilities 

  • Strong knowledge of cGMP requirements, GDP practices, SOP compliance, and pharmaceutical manufacturing operations. 

  • Understanding of FDA, DEA, OSHA, and hazardous material handling requirements. 

  • Ability to read, understand, and execute batch records, SOPs, cleaning procedures, and safety documentation in English. 

  • Ability to accurately complete GMP documentation and perform batch accountability calculations. 

  • Strong mathematical skills include percentages, ratios, decimals, and yield calculations. 

  • Mechanical aptitude and ability to assemble/disassemble manufacturing equipment. 

  • Strong attention to detail and ability to identify process deviations or abnormalities. 

  • Ability to work independently with minimal supervision while maintaining a high level of accuracy and compliance. 

  • Effective communication and teamwork skills. 

  • Basic computer literacy and familiarity with electronic manufacturing systems preferred. 

     Physical Requirements and Working Conditions 

  • Ability to stand, walk, bend, reach, climb, and perform repetitive movements throughout the shift. 

  • Ability to frequently lift, push, pull, and move materials or equipment up to 50 pounds. 

  • Regular exposure to manufacturing equipment, moving mechanical parts, solvents, airborne particles, potent compounds, and cleaning chemicals. 

  • Required use of personal protective equipment (PPE), including respirators, full-body coveralls, gloves, hearing protection, and eye protection. 

  • Ability to work in classified manufacturing environments with varying temperatures, humidity, and noise levels. 

  • Ability to work overtime, weekends, holidays, or alternate shifts as operationally required. 

Medical Surveillance / Respiratory Protection Requirement 

As a condition of employment, employees assigned to this position may be required to wear respiratory protection equipment while performing manufacturing, cleaning, dispensing, or material handling activities involving potent compounds, pharmaceutical powders, airborne particulates, solvents, or other hazardous materials. 

In accordance with OSHA Respiratory Protection Standard 29 CFR 1910.134, employees required to wear respirators must complete a medical evaluation questionnaire consistent with Appendix C of the standard and be medically cleared to wear a respirator prior to performing applicable job duties. Additional evaluations may be required as determined by Environmental Health & Safety (EHS), Occupational Health, or regulatory requirements. 

Employees must also comply with all applicable respiratory protection, PPE, safety training, and fit-testing requirements established by the company and regulatory agencies.