OQ jobs in Florida

Manufacturing Engineer Medical Devices (IQ/OQ/PQ Focus)

Gainesville, Florida

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Today

Title: Manufacturing Engineer Medical Devices (IQ/OQ/PQ Focus) Location: Gainesville, FL (On-site) Duration: Long Term Contract Position Summary: Our client is seeking a highly skilled Manufacturing Engineer with a strong background in the medical device industry and extensive experience in IQ/OQ/PQ validation activities. The successful candidate will ensure that manufacturing processes meet regulatory requirements, improve efficiency, and maintain the highest quality standards. Key Responsibili

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Contract

Depends on Experience

Manufacturing Engineer Medical Devices (CNC Machining Focus)

Gainesville, Florida

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Today

Title: Manufacturing Engineer Medical Devices (CNC Machining Focus) Location: Gainesville, FL (On-site) Duration: Long Term Contract Position Summary: We are looking for an experienced Manufacturing Engineer with a strong background in CNC machining for precision medical device components. The candidate will be responsible for developing, optimizing, and validating CNC machining processes to meet stringent quality and regulatory requirements. Key Responsibilities: Develop, program, and optimize

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Contract

Depends on Experience

Sr. Engineer, Packaging

Remote or El Paso, Texas

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Today

What Packaging Engineering contributes to Cardinal Health Packaging Engineering is responsible for designing, developing and testing a wide variety of equipment and packaging used for protection, display and handling of products. Determines packaging specifications, cost limitations, legal requirements, and related documentation. Directs external resources / contractors as required. The ideal candidate would be located in the El Paso, Texas area and this position is a hybrid role. Responsibilit

Full-time

USD 67,500.00 - 96,400.00 per year

Computer System Validation (CSV) Engineer

Remote or Massachusetts

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Today

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. Author and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's

Full-time

Senior Commissioning, Qualification & Validation (CQV) Engineer

Remote or Athens, Georgia

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

Validation Engineer

Sarasota, Florida

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Today

Job Description: Protocol Review & Compliance: Study and assess Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports for regulatory and procedural compliance. Process Audits & Documentation: Conduct thorough audits of manufacturing processes to identify documentation gaps. Update Quality Management System (QMS) documents to reflect findings and ensure alignment with current standards. Process Optimization: Design and execute De

Full-time

Process Quality Engineer

St. Petersburg, Florida

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Today

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processe

Full-time

Manufacturing Engineer

Gainesville, Florida

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13d ago

Role: Manufacturing Engineer Location: Gainesville, FL & Sarasota, FL Experience: 8 Years Durations: 6+ Months Positions: 8 Skills: IQ-OQ-PQ Experience in medical parts manufacturing experience is the key, with process validation expertise around 8 to 10 yrs experience, and Medical Device experience is mandatory. with hands-on experience in CNC Machining and DCM.

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Full-time

$40 - $50

Process Quality Engineer (1pm-10pm)

St. Petersburg, Florida

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Today

Full-time

Sr. Analyst, IT Validation Services

Remote or Hybrid in Stamford, Connecticut

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Today

Job Title: Sr. Analyst, IT Validation Services Location: Remote Duration: 12 Months Pay Range: $30/hr-$35/hr on W2 (DOE) Primary Responsibilities Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls: Validation Plans/Summary Reports Risk Assessments User Requirements Specifications Test Plans Test Scripts: IQ, OQ or PQ Assess and implement the most effective validation strategy for each activity. Oversee test execution for c

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Contract

BASED ON EXPERIENCE

Senior Engineering Manager, Scientific Injection Molding Development and Training

Remote

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Today

Full-time

USD 135,700.00 - 244,300.00 per year

Computer System Validation Engineer

Remote or New Jersey

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Today

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles. Compliance Analysis, Validation Planning, Risk Assessments Test planning and strategy creation and execution of test protocols, scripts and reports. V

Full-time

Validation Lead, SAP S4 HANA

Remote or New Jersey

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Today

Responsibilities: Lead the validation team in a strategic, risk-based approach that optimizes legacy Computer System documentation, CSA strategies and strong SAP ECC->S/4 HANAconversion knowledge to successfully deliver a validated system meeting all project requirements. Review, approval, and processing of Computer System Lifecycle deliverables including: User Requirements, Specifications, Test Plans, IQ, OQ, PQ Test Scripts, User Guides. Fostering of effective relationships with implementati

Full-time

Computer System Validation Analyst - R Studio & Clinical Systems

Remote or New Jersey

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Today

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Full-time

Manufacturing Engineer (Sarasota, FL)

Sarasota, Florida

•

Yesterday

Role: Manufacturing Engineer Location: Gainesville, FL & Sarasota, FL Experience: 8 Years Durations: 6+ Months Skills: IQ-OQ-PQ Experience in medical parts manufacturing experience is the key, with process validation expertise around 8 to 10 yrs experience, and Medical Device experience is mandatory. Job Description: Protocol Review & Compliance: Study and assess Installation Qualification (IQ), Operational Qualification (OQ),and Performance Qualification (PQ) protocols and reports for regulato

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Contract

Depends on Experience

LIMS and QC Applications Consultant

Remote or Hybrid in Bridgewater, New Jersey

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Today

Solution Architecture and Design: Lead the design and development of LabVantage LIMS solutions tailored to business and laboratory needs. Develop system workflows, configurations, and integrations with other enterprise systems (e.g., S4 Hana ERP, MES, ELN, SDMS). Define data models, interface designs, and system configurations. Implementation and Deployment: Oversee installation, configuration, and validation of LabVantage LIMS applications. Develop and execute project plans, ensuring timely an

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Full-time, Contract

BASED ON EXPERIENCE

Senior Engineer, Design Transfer Specialist

Remote or Cambridge, Massachusetts

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Today

Career Category Operations Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each

Full-time

USD 119,195.00 per year

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OQ jobs in Florida, USA