Process Engineer
Juncos, PR · On-site
The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes. Responsibilities: * Develop and execute validation activities for ...
Process Engineer
Juncos, PR · On-site
The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes. Responsibilities: * Develop and execute validation activities for ...
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 ...
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)
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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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 ...
Data Center OQ/QA Coordinator
Houston, TX · On-site
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
Houston, TX · On-site
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 ...
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 ...
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 ...
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
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 ...
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 ...
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 ...
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)
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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Key Responsibilities: • Supplier Risk Classification & Risk Assessment • FDA Remediation & Supplier Quality Improvement • DFMEA, PFMEA & Risk Management • Supplier Process Validation (IQ/OQ ...
Installation, Operational, and Performance Qualifications (IQ/OQ/PQ) * Requirements Traceability Matrix (RTM) * Final/Summary Reports * Support equipment lifecycle validation activities for ...
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Installation, Operational, and Performance Qualifications (IQ/OQ/PQ) * Requirements Traceability Matrix (RTM) * Final/Summary Reports * Support equipment lifecycle validation activities for ...
Validation Engineer / Specialist (Greater Boston)
Waltham, MA · On-site
$75K - $105K/yr
Support IQ, OQ, PQ protocols for lab systems, equipment, and utilities * Partner with lab teams, engineers, and managers to understand systems * Assist with project scheduling, resource planning, and ...
Validation Engineer / Specialist (Greater Boston)
Waltham, MA · On-site
$75K - $105K/yr
Support IQ, OQ, PQ protocols for lab systems, equipment, and utilities * Partner with lab teams, engineers, and managers to understand systems * Assist with project scheduling, resource planning, and ...
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 & Poly Fusion Training Instructor The OQ and Fusion Instructor is responsible for teaching Operator Qualifications (OQ) and Fusion Training courses to customers, utilizing existing training ...
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OQ & Poly Fusion Training Instructor The OQ and Fusion Instructor is responsible for teaching Operator Qualifications (OQ) and Fusion Training courses to customers, utilizing existing training ...
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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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 ...
US - Manufacturing Engineer-Sr
$88K - $120K/yr
Equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA) Cleaning validations (IQ, OQ, PQ) * Coordinate the arrangement of machines within plant facilities to ensure most ...
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US - Manufacturing Engineer-Sr
$88K - $120K/yr
Equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA) Cleaning validations (IQ, OQ, PQ) * Coordinate the arrangement of machines within plant facilities to ensure most ...
Execute equipment requalification (IQ/OQ/PQ) per cGMP standards * Review and update calibration and maintenance records * Identify and recommend remediation activities as needed Requirements:
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Execute equipment requalification (IQ/OQ/PQ) per cGMP standards * Review and update calibration and maintenance records * Identify and recommend remediation activities as needed Requirements:
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
How much do oq jobs pay per hour?
As of Jul 22, 2026, the average hourly pay for oq in the United States is $17.32, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $19.23 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as an Oq, and why are they important?
I'm sorry, but 'Oq' does not correspond to a recognized real-world professional occupation, so I cannot provide an accurate response.
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.
What are Oq jobs?
The term 'Oq' does not correspond to a widely recognized job title or profession. It is possible that 'Oq' is a typographical error, an acronym, or a company-specific designation. If you are looking for information about a specific job or industry, please provide additional context or clarify the term.
More about Oq jobs
What states have the most Oq jobs? States with the most job openings for Oq jobs include:
What job categories do people searching Oq jobs look for? The top searched job categories for Oq jobs are:
Full-time
Posted 21 days ago
Job description
EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.
We are seeking Process Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes.
Responsibilities:
Minimum Requirements:
*This opportunity will be full-time 100% on site in East, Puerto Rico.
*Remote and hybrid work arrangements are not available for this position.
We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion and ready to represent EQVAL Group, we would love to hear from you. Apply now!!
EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.
We are seeking Process Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes.
Responsibilities:
- Develop and execute validation activities for equipment and process changes (IQ, OQ, PQ) and associated documentation.
- Optimize manufacturing processes, ensuring efficient production layouts, material handling, and tool fabrication.
- Troubleshoot and improve production equipment and processes to enhance operational efficiency and product quality.
- Collaborate with cross-functional teams to support investigations (NCRs, Complaints) and implement corrective actions.
- Ensure compliance with regulatory standards (cGMP) in all manufacturing processes and validation activities.
Minimum Requirements:
- Bachelor's Degree in Engineering.
- Experience in developing and executing validation documentation (Validation Plans, URS, FRS, IQ, OQ, PQ).
- Experience in investigations (NCRs, Complaints, CAPA), Lean Manufacturing, and Six Sigma tools.
- Experience with pFMEA (analysis and development) and its application.
- Fully bilingual (English and Spanish) spoken and written.
- Good technical writing skills.
*This opportunity will be full-time 100% on site in East, Puerto Rico.
*Remote and hybrid work arrangements are not available for this position.
We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion and ready to represent EQVAL Group, we would love to hear from you. Apply now!!
EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.