Blender Operator I
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AVEVA DRUG DELIVERY SYSTEMS INC
FL
Summary
Perform pharmaceutical blending and compounding operations using APIs and hazardous materials in a cGMP-regulated environment. Responsible for equipment setup, material dispensing, and maintaining accurate GMP documentation.
Job Description
Job DetailsJob Location: Miramar, FL 33025Salary Range: $21.00Job Shift: Swing
Job Description
Job Title (Internal)
Blender Operator I
Job Profile/Level:
Line of Business (LOB) or Business Process Stream (BPS)
Department/Org Unit:
Production Operations
Reports Directly To:
Supervisor/Sr. Supervisor, Production Operations
Reports Indirectly To:
People Leader
Yes No
Number of Direct Reports and Job Titles
Revision Date
(Month / Day / Year)
05/13/2026
Revision Number:
Job Location:
Travel Requirements
Yes
No
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.
QualificationsJob Requirements
Education
High school diploma or General Education Degree (GED) required.
Technical certification or vocational training in manufacturing, pharmaceutical operations, or related discipline preferred.
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Founded
2003
Company size
201-500 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Miramar, FL
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Founded
2003
Company size
201-500 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Miramar, FL