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Oq Jobs in Indiana (NOW HIRING)

Eliquent Life Sciences, Inc

CQV Engineer

Indianapolis, IN · On-site

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Validation protocol execution for FAT/SAT/IQ/OQ/PQ, thermal mapping of temperature-controlled chambers, warehouses, and sterilization processes * Equipment Qualification test execution

ATS Automation

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

The Quality Engineer supports Comecer Project Managers in the management of the orders from a quality point of view throughout the project including design reviews, FAT, SAT, IQ, OQ and some aspects ...

PinnaclePartners

Quality Assurance Engineer

Indianapolis, IN

$95K - $103K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Partner with Engineering and Manufacturing to execute IQ, OQ, and PQ validation activities. Support supplier qualification activities, supplier audits, and Supplier Corrective Action Requests (SCARs)

Piezo Technologies

Manufacturing Engineer

Indianapolis, IN · On-site

$80K - $105K/yr

Conduct capability studies and equipment/process qualifications including IQ, OQ, and PQ activities. * Support compliance with ISO 9001, ISO 13485, and applicable regulatory requirements. * Identify ...

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

The role requires strong hands-on experience executing IQ, OQ, PQ, and test scripts; documenting objective evidence; managing protocol exceptions and deviations; and ensuring laboratory systems are ...

PM Group

CSV Engineer III

Indianapolis, IN

$68K - $88K/yr

The role requires strong hands-on experience executing IQ, OQ, PQ, and test scripts; documenting objective evidence; managing protocol exceptions and deviations; and ensuring laboratory systems are ...

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Showing results 21-40

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Oq information

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How much do oq jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for oq in Indiana is $16.48, according to ZipRecruiter salary data. Most workers in this role earn between $14.18 and $18.32 per hour, depending on experience, location, and employer.

What is an Oq?

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.

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?

AspectOqData Analyst
Required CredentialsTypically requires a degree in engineering, computer science, or related fieldsUsually requires a degree in statistics, mathematics, or related fields
Work EnvironmentOften in industrial, manufacturing, or engineering settingsPrimarily in business, finance, or tech sectors
Employer & Industry UsageUsed in engineering, manufacturing, and infrastructure projectsCommon in corporate, finance, marketing, and tech industries
Common Search & Comparison IntentUnderstanding technical roles in engineering and infrastructureAnalyzing 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 popular job titles related to Oq jobs in Indiana?

For Oq jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Oq jobs in Indiana look for?

The top searched job categories for Oq jobs in Indiana are:

Oq jobs near you
Infographic showing various Oq job openings in Indiana as of August 2026, with employment types broken down into 85% Full Time, 5% Part Time, 1% Temporary, 8% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $34,274 per year, or $16.5 per hour.

Senior CSV Validation Specialist (Building Management Systems)

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 9 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Sr CSV Validation Specialist position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Senior CSV Validation Specialist (Building Management Systems)

Location: Indianapolis, IN (100% Onsite)
Duration: Long Term
 

Job Overview

We are seeking an experienced Senior CSV Validation Specialist to support Building Management System (BMS) validation within a regulated pharmaceutical manufacturing environment. This role will lead the full Computer System Validation (CSV) lifecycle, ensuring compliance with FDA, EMA, and GAMP 5 requirements while partnering with Automation, IT, Engineering, and System Integrators.

Key Responsibilities

  • Lead end-to-end validation of Building Management Systems (BMS) from URS through Validation Summary Reports.
  • Author and execute validation documentation including URS, DQ, IQ, OQ, PQ, RTM, Validation Plans, and VSRs.
  • Review software requirements and collaborate with vendors, including Johnson Controls, on system validation activities.
  • Perform 21 CFR Part 11 assessments for electronic records, audit trails, and electronic signatures.
  • Validate integrations between Metasys, AVEVA PI, DeltaV, and OPC UA platforms.
  • Support commissioning, qualification, system acceptance testing, and periodic reviews.
  • Develop SOPs and maintain validation documentation in an inspection-ready state.
  • Support audit readiness, data integrity initiatives, remediation activities, and future system upgrades.
  • Collaborate with Automation, IT, Engineering, Quality, and Validation teams to ensure GMP compliance.

Required Qualifications

  • Strong experience in Computer System Validation (CSV) within pharmaceutical or GMP-regulated environments.
  • Hands-on experience validating Building Management Systems (BMS) or industrial control systems.
  • In-depth knowledge of GAMP 5, V-Model lifecycle, and risk-based validation methodologies.
  • Experience with 21 CFR Part 11 compliance and computerized system validation.
  • Proven experience authoring and executing CSV documentation, including URS, FS, DS, IQ, OQ, PQ, RTM, Validation Plans, and Validation Summary Reports.
  • Experience supporting BMS, DCS, PLC, HMI, or Historian systems.
  • Strong understanding of FDA and EMA regulatory requirements.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com