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Assistant Cleaning Validation Engineer Jobs in Florida

Actalent

Validation Specialist

Boca Raton, FL · On-site

$36.06 - $45.67/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Familiarity with cleaning validation principles and practices. * Experience collaborating with cross-functional teams including Engineering, Production, Quality Control, Microbiology, and Quality ...

ADMA BIOMANUFACTURING LLC

Associate, Validation

Boca Raton, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... cleaning, checks, and tests during the manufacturing process. This role also compiles, interprets ... You will also identify, communicate, and assist in the execution of various validation protocols.

CEDENT

Process Engineer

Largo, FL

Lead and/or support cleaning validation and process validation efforts and projects, as needed to support commercial operations. * Identify and lead continuous improvement engineering projects to ...

Cedent

Process Engineer (Largo, FL)

Largo, FL · On-site

Lead and/or support cleaning validation and process validation efforts and projects, as needed to support commercial operations. * Identify and lead continuous improvement engineering projects to ...

CEDENT

Process Engineer (Largo, FL)

Largo, FL · On-site

Lead and/or support cleaning validation and process validation efforts and projects, as needed to support commercial operations. Identify and lead continuous improvement engineering projects to ...

Kett Engineering

Be Seen First

Autonomous Systems Validation Operator

Miami, FL · On-site

$24 - $27/hr

Kett Engineering is working with a major EV manufacturer, and we are hiring multiple Autonomous ... Clean driving record: No suspensions/revocations within the last 3-5 years. * No drug or alcohol ...

Kett Engineering

Be Seen First

Autonomous Systems Validation Operator

Miami, FL · On-site

$24 - $27/hr

Kett Engineering is working with a major EV manufacturer, and we are hiring multiple Autonomous ... Clean driving record: No suspensions/revocations within the last 3-5 years. * No drug or alcohol ...

Unicon Pharma Inc.

MS&T Specialist I

Davie, FL · On-site

The Microbiology & Cleaning Validation Associate supports MS&T activities related to ... Collaborate cross-functionally with MS&T, QA, QC, Engineering, and Manufacturing teams. Education ...

Kidde Global Solutions

Eng. Test & Validation

Bradenton, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

You will also use your technical skills to support product validation within Global Lab ... Work with cross-functional engineering teams to assist in complex route cause analysis to create ...

ReturnPro

Data Engineer

Miami, FL · On-site

$109K - $131K/yr

ReturnPro is seeking an experienced Data Engineer to lead the design, development, and optimization ... cleaning, validation, and transformation techniques. • Lead the implementation of big data ...

ReturnPro

Data Engineer

Aventura, FL · On-site

$109K - $131K/yr

We are seeking an experienced Data Engineer to lead the design, development, and optimization of ... cleaning, validation, and transformation techniques. Cloud and Big Data Solutions · Lead the ...

ReturnPro

Data Engineer

Aventura, FL · On-site

$109K - $131K/yr

We are seeking an experienced Data Engineer to lead the design, development, and optimization of ... cleaning, validation, and transformation techniques. Cloud and Big Data Solutions • Lead the ...

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All JobsCleaning Validation Engineer JobsAssistant Cleaning Validation Engineer JobsAssistant Cleaning Validation Engineer Jobs in Florida

Assistant Cleaning Validation Engineer information

What is the difference between Assistant Cleaning Validation Engineer vs Cleaning Validation Engineer?

AspectAssistant Cleaning Validation EngineerCleaning Validation Engineer
CredentialsTypically requires a bachelor's degree in life sciences or engineering; certifications like ASQ or GMP training are commonRequires similar qualifications; often more experience or advanced certifications
Work EnvironmentSupports validation activities in pharmaceutical or biotech manufacturing facilitiesLeads validation projects, performs complex testing, and reviews validation protocols
Employer & IndustryPharmaceutical, biotech, or medical device companiesSame industries, with more senior responsibilities

The Assistant Cleaning Validation Engineer typically supports validation tasks under supervision, focusing on executing protocols and data collection. In contrast, the Cleaning Validation Engineer oversees validation processes, reviews results, and ensures compliance. Both roles are essential in maintaining product quality and regulatory standards in pharmaceutical manufacturing.

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Assistant Cleaning Validation Engineer jobs near you

Equipment Validation Engineer

ASI Systems Engineering

Tampa, FL • On-site

Full-time

Posted 20 days ago

Job description


Equipment Validation Engineer
Location: Tampa, FL - onsite
Contract: 6 months
Job Summary
ASI is seeking an Equipment Validation Engineer to support oral solid dose pharmaceutical manufacturing operations in Tampa, Florida. The engineer will develop, execute, and evaluate qualification and validation activities demonstrating that facilities, manufacturing equipment, packaging equipment, and associated processes operate consistently and in compliance with cGMP requirements. The role includes authoring and executing IQ/OQ/PQ protocols and summary reports, supporting validation project planning, and coordinating with Engineering, Manufacturing, Quality, Maintenance, and external vendors to integrate validation activities into project and production schedules.
Relevant Equipment Experience
Experience with oral solid dose process and packaging equipment is desirable, including:
• Fluid bed dryers
• Granulators, including high-shear granulation equipment
• Pharmaceutical mills, including cone and hammer mills
• Bottle fillers
• Blister fillers
• Cappers
• Labelers and barcode systems
• Cartoners
• Case packers
Responsibilities
• Develop, execute, and analyze equipment and process validation projects supporting cGMP compliance.
• Author and execute IQ, OQ, and PQ protocols and associated summary reports for manufacturing and packaging equipment.
• Author or support change controls, SOPs, work instructions, and validation lifecycle documentation.
• Provide technical support for deviations, CAPAs, investigations, and equipment or process changes.
• Design and execute process and cleaning validation studies in accordance with site procedures and industry standards.
• Support equipment startup, product changeovers, troubleshooting, and continuous improvement initiatives.
• Coordinate with internal and external technical personnel to establish priorities, schedules, responsibilities, and practical validation approaches.
Requirements
Qualifications
• Bachelor's degree in Engineering, Pharmacy, Science, or a related technical discipline.
• Two or more years of experience in life sciences engineering, manufacturing, or validation.
• At least one year of direct equipment qualification or validation experience.
• Experience working in an FDA-regulated, cGMP-compliant manufacturing environment.
• Experience with oral solid dose manufacturing or packaging equipment is strongly preferred.
• Strong technical writing, collaboration, communication, and organizational skills.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.

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