Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM)
Validation Specialist
Indianapolis, IN · On-site
We are seeking professionals with experience in GMP equipment validation and qualification, IQ/OQ protocol development and execution, HPLC and laboratory instrumentation, validation lifecycle ...
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Validation Specialist
Indianapolis, IN · On-site
We are seeking professionals with experience in GMP equipment validation and qualification, IQ/OQ protocol development and execution, HPLC and laboratory instrumentation, validation lifecycle ...
Senior Molding Manufacturing Engineer
Libertyville, IL · On-site
$101K - $130K/yr
Lead validation activities ( IQ/OQ/PQ ) and mold qualifications. * Participate in FAT/SAT activities for new molds and equipment. * Collaborate with Design, Quality, and Production teams on ...
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Apply Early
Senior Molding Manufacturing Engineer
Libertyville, IL · On-site
$101K - $130K/yr
Lead validation activities ( IQ/OQ/PQ ) and mold qualifications. * Participate in FAT/SAT activities for new molds and equipment. * Collaborate with Design, Quality, and Production teams on ...
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Develop and execute process validation protocols (IQ, OQ, PQ). * Support manufacturing process improvements and process transfers. * Ensure compliance with FDA, ISO 13485, and GMP regulations.
Develop and execute process validation protocols (IQ, OQ, PQ). * Support manufacturing process improvements and process transfers. * Ensure compliance with FDA, ISO 13485, and GMP regulations.
Prepare IQ/OQ and /or PQ protocols for various Cell Therapy manufacturing process equipment and QC test equipment such as Flow Cytometers, Cell Separators, Centrifuges, Cell processing equipment ...
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Prepare IQ/OQ and /or PQ protocols for various Cell Therapy manufacturing process equipment and QC test equipment such as Flow Cytometers, Cell Separators, Centrifuges, Cell processing equipment ...
Apply Early
Senior Manufacturing Engineer
Irvine, CA · On-site
$97K - $133K/yr
Key Responsibilities: • Lead IQ, OQ & PQ equipment validation • Manage third-party vendors and engineering projects • Design & validate chemical mixing systems • Interpret engineering ...
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Senior Manufacturing Engineer
Irvine, CA · On-site
$97K - $133K/yr
Key Responsibilities: • Lead IQ, OQ & PQ equipment validation • Manage third-party vendors and engineering projects • Design & validate chemical mixing systems • Interpret engineering ...
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URS/FDS/DDS review, risk assessments, test protocols (IQ/OQ), and summary reports. * Supplier assessment execution for OEMprovided computerized systems. * Data integrity assessment using ALCOA ...
URS/FDS/DDS review, risk assessments, test protocols (IQ/OQ), and summary reports. * Supplier assessment execution for OEMprovided computerized systems. * Data integrity assessment using ALCOA ...
Mechanical Process Validation (IQ, OQ, PQ, TMV, G R&R, Equipment Software Validation). * FDA (21 CFR, Part 820). * Statistical Analysis Tools such as Minitab. * CAD modeling (Preferred Solidworks)
Mechanical Process Validation (IQ, OQ, PQ, TMV, G R&R, Equipment Software Validation). * FDA (21 CFR, Part 820). * Statistical Analysis Tools such as Minitab. * CAD modeling (Preferred Solidworks)
Business Introduction: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines ...
Business Introduction: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines ...
Equipment Engineer
Billerica, MA · On-site
Change Order Management Equipment Validation (IQ/OQ/PQ) Calibration & Metrology Expertise Equipment Maintenance & Troubleshooting Root Cause Analysis & CAPA Manufacturing Equipment Qualification ...
Equipment Engineer
Billerica, MA · On-site
Change Order Management Equipment Validation (IQ/OQ/PQ) Calibration & Metrology Expertise Equipment Maintenance & Troubleshooting Root Cause Analysis & CAPA Manufacturing Equipment Qualification ...
Sr Process Engineer
Boulder, CO · On-site
$48 - $50/hr
Validate changes (IQ, OQ, PQ) * Troubleshoot equipment and systems * Ensure regulatory compliance * Lead capital equipment projects * Support new technology integration * Drive continuous improvement
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Sr Process Engineer
Boulder, CO · On-site
$48 - $50/hr
Validate changes (IQ, OQ, PQ) * Troubleshoot equipment and systems * Ensure regulatory compliance * Lead capital equipment projects * Support new technology integration * Drive continuous improvement
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Key Responsibilities: • Supplier Risk Classification & Risk Assessment • FDA Remediation & Supplier Quality Improvement • DFMEA, PFMEA & Risk Management • Supplier Process Validation (IQ/OQ ...
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Apply Early
Key Responsibilities: • Supplier Risk Classification & Risk Assessment • FDA Remediation & Supplier Quality Improvement • DFMEA, PFMEA & Risk Management • Supplier Process Validation (IQ/OQ ...
Apply Early
Change Order Management Equipment Validation (IQ/OQ/PQ) Calibration & Metrology Expertise Equipment Maintenance & Troubleshooting Root Cause Analysis & CAPA Manufacturing Equipment Qualification ...
Change Order Management Equipment Validation (IQ/OQ/PQ) Calibration & Metrology Expertise Equipment Maintenance & Troubleshooting Root Cause Analysis & CAPA Manufacturing Equipment Qualification ...
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Data Center OQ/QA Coordinator
$30 - $33/hr
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Data Center OQ/QA Coordinator
$30 - $33/hr
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Data Center OQ/QA Coordinator
$30 - $33/hr
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Quick apply
Apply Early
Data Center OQ/QA Coordinator
$30 - $33/hr
Duties and Responsibilities: * Monitors in-house installation teams as well as subcontract actions for contract compliance, monitors risk and contributes suggestions for risk mitigation * Facilitates ...
Apply Early
Business Introduction: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines ...
Business Introduction: We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines ...
Urgent On-Site Opening for Senior CQV Engineer - Needham, MA - Need Local to MA Only.
Needham, MA · On-site
This role will focus on drafting and executing URS, IQ, OQ, PQ, and commissioning protocols, ensuring equipment, utilities, and lab spaces are compliant with FDA/EMA requirements and fully audit ...
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Apply Early
Urgent On-Site Opening for Senior CQV Engineer - Needham, MA - Need Local to MA Only.
Needham, MA · On-site
This role will focus on drafting and executing URS, IQ, OQ, PQ, and commissioning protocols, ensuring equipment, utilities, and lab spaces are compliant with FDA/EMA requirements and fully audit ...
Apply Early
Manufacturing Engineer II
Saint Paul, MN · On-site
$40 - $43/hr
Execute and support equipment qualifications (IQ/OQ/PQ) * Assist with line transfers, line duplication, or equipment moves * Work cross-functionally with engineering and quality teams to ensure ...
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Manufacturing Engineer II
Saint Paul, MN · On-site
$40 - $43/hr
Execute and support equipment qualifications (IQ/OQ/PQ) * Assist with line transfers, line duplication, or equipment moves * Work cross-functionally with engineering and quality teams to ensure ...
Oq information
See salary details
$11.78 - $12.78
2% of jobs
$12.78 - $13.79
6% of jobs
$13.79 - $14.79
16% of jobs
$14.84 is the 25th percentile. Wages below this are outliers.
$14.79 - $15.80
13% of jobs
$15.80 - $16.81
11% of jobs
The median wage is $16.96 / hr.
$16.81 - $17.81
14% of jobs
$17.81 - $18.82
9% of jobs
$19.16 is the 75th percentile. Wages above this are outliers.
$18.82 - $19.82
14% of jobs
$19.82 - $20.83
10% of jobs
$20.83 - $21.83
4% of jobs
$21.83 - $22.84
2% of jobs
$11
$17
$22
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What is the difference between Oq vs Data Analyst?
| Aspect | Oq | Data Analyst |
|---|---|---|
| Required Credentials | Typically requires a degree in engineering, computer science, or related fields | Usually requires a degree in statistics, mathematics, or related fields |
| Work Environment | Often in industrial, manufacturing, or engineering settings | Primarily in business, finance, or tech sectors |
| Employer & Industry Usage | Used in engineering, manufacturing, and infrastructure projects | Common in corporate, finance, marketing, and tech industries |
| Common Search & Comparison Intent | Understanding technical roles in engineering and infrastructure | Analyzing data to inform business decisions |
Oq and Data Analyst roles share some overlap in data handling and analysis but differ mainly in industry focus and required credentials. Oq is more technical and engineering-oriented, while Data Analysts focus on interpreting data for business insights.
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Posted 6 days ago
Job description
Position Overview
Technical & Engineering Consulting is seeking a qualified candidate to support inventory analysis and define the scope of remediation activities across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM). This role will leverage automated tools and collaborate with site-level subject matter experts to ensure data accuracy, completeness, and alignment with current validation standards and remediation requirements.
Key Responsibilities
- Utilize automated tools to extract, filter, and organize validation documentation (e.g., Windchill to Excel trackers) for remediation assessment activities.
- Review and validate extracted data to ensure accuracy, completeness, and alignment with site practices and documentation.
- Perform detailed assessments to identify remediation scope across Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM).
- Apply technical judgment to confirm the applicability of validation records and identify discrepancies such as missing, conflicting, or outdated documentation.
- Cross-check validation records against Master Validation Plans (MVPs), Product Risk Assessments (PRAs), and other supporting validation documents.
- Identify, quantify, and prioritize products or processes requiring remediation, including high-risk, complex, or ambiguous scenarios.
- Ensure alignment with current procedures, global validation standards, and remediation expectations and timelines.
- Proactively identify data gaps, inconsistencies, and tool limitations, and escalate risks, uncertainties, or blockers to the core team in a timely manner.
- Document findings clearly and provide recommendations to support effective remediation planning and execution.
Qualifications
- Bachelor's degree in Engineering, Life Sciences, or related field
- 3+ years of experience in:
- Validation (OQ/PQ/TMV/IPM)
- Quality Engineering or Manufacturing Engineering
- Strong understanding of Validation lifecycle and documentation and Regulated environments (FDA, ISO, GMP)
- Experience with Data analysis tools (Excel - advanced) and Document management systems (e.g., Windchill preferred)