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Hourly Pharma Validation Engineer Jobs in Indiana

RADcube

Data Analyst

Indianapolis, IN · On-site

$75 - $110/hr

... pharma-focused data team. This role focuses on turning large, complex datasets into clear ... You will work closely with data engineering teams to access and shape data from modern cloud ...

Simotechnology

Senior OSI PI Engineer

Indianapolis, IN · On-site

$90 - $120/hr

* Industry Pharma/Biotech/Clinical Research * City Indianapolis * Province Indiana * Country United ... Knowledge ofGMP'S, regulatory requirements, computer system validation. * Interfaceregularly and ...

Thermo Fisher Scientific

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

... IN - Pharma Services Group Discover Impactful Work: The Quality Engineer is responsible for ... Works with FCS sites to assure consistency in validation strategy/approach for local and global ...

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

The CSV Engineer III will support validation activities for systems used in quality control ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

The CSV Engineer III will support validation activities for systems used in quality control ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

Thermo Fisher Scientific

Quality Engineer

Indianapolis, IN

$68K - $88K/yr

... IN - Pharma Services Group Discover Impactful Work: The Quality Engineer is responsible for ... Works with FCS sites to assure consistency in validation strategy/approach for local and global ...

System One

Cloud Engineer

Indianapolis, IN · On-site

$53.25 - $71.25/hr

... deployments with testing, validation, safe releases, and rollback strategies. * Automate ... Regulated-industry experience (pharma/healthcare/life sciences), including compliance ...

System One

Cloud Engineer

Indianapolis, IN · On-site

$53.25 - $71.25/hr

... deployments with testing, validation, safe releases, and rollback strategies. * Automate ... Regulated-industry experience (pharma/healthcare/life sciences), including compliance ...

System One Holdings, LLC

Cloud Engineer

Indianapolis, IN · On-site

$92.02 - $105.10/hr

... deployments with testing, validation, safe releases, and rollback strategies. * Automate ... Regulated-industry experience (pharma/healthcare/life sciences), including compliance ...

System One

Cloud Engineer

Indianapolis, IN · On-site

$53.25 - $71.25/hr

... deployments with testing, validation, safe releases, and rollback strategies. * Automate ... Regulated-industry experience (pharma/healthcare/life sciences), including compliance ...

Elanco

Process Automation Engineer

Clinton, IN · On-site

Process Automation Engineer As a Process Automation Engineer, you will support the Clinton ... pharma, biotech, food, or similar) * Knowledge of computer system validation (CSV) and change ...

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Infographic showing various Hourly Pharma Validation Engineer job openings in Indiana as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution.

Quality Engineer

ATS Automation Tooling Systems Inc

Indianapolis, IN • On-site

$70 - $90/hr

Other

Posted 14 days ago

Job description

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Requisition ID: 17601


Location: Indianapolis, IN, US, 46250


Date: Aug 7, 2026


Quality Engineer
Job Description

The Quality Engineer supportsComecerProject 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 of PQ as they relate to VPHP cycle development.


The markets this position services include Radiopharma, Pharma and Cell & Gene Therapy (ATMP) projects in North America; including, but are not limited to:


Radiopharma – shielded hot cells and automation, synthesis and dispensing modules for vials and syringes, LAF shielded isolators, sterility testing isolators, VPHP generators for sterilization, solid target processing systems, dose calibrators, glove testers, and VPHP sterilization modules


Pharma –aseptic handling and filling of liquid and powder APIs, dispensing custom R&D isolators, potent API processing Isolators (PAPI), modular sterility testing isolators (MSTI), ATEX isolators, Baby Phill small batch vial filling, Combo Phill aseptic filling line for RTU vials syringes, cartridges, fully automated combination product end-to-end filling systems, Speedy Glove,DeconBox™


Cell & Gene Therapy (ATMP) – modular cell culture isolator (MCCI), incubation system for advanced therapy labsFlexyCult™


Additional Information

ESSENTIAL JOBDUTIES:


Quality



  • Supportcolleaguesin draftingandfinalizingtechnical documents and the interpretation and application of legal, regulatory and project requirements

  • Quality management of orders in relation to:

  • Specific validation (DQ)

  • Process controls

  • Work with technical team in the field as well as 3rdparties at customer sites to perform and successfully complete SAT, IQ, OQ, VPHP Cycle development and VPHP PQ activities.

  • Work with other colleagues to develop andmaintainquality procedures and controls atComecerInc. facilities in North America to conform to customer and regulatory requirements.

  • Work withComecerquality personnel and 3rdparties to establishregulatory approval forComecerdisposable kits for sale in North America

  • Develop inspection methods to analyze product quality

  • Implement a working system to ensure conformity and accuracy in the production process

  • Ensure products compliance with company and international quality standards

  • Ensure that the product corresponds to the desired technical specifications and take corrective action to resolve non-conformities

  • Plan and document control activities and inspections

  • Other duties asrequired.


Qualifications

QUALIFICATIONS:



  • Bachelor’s degree in technical field or equivalent experience.

  • Quality Engineering experience in a manufacturing environmentpreferred.

  • Experience withInternational Standardization Organization(ISO) standards9001preferred.

  • Ability to communicate efficiently and effectively with people at all levels of the organization, both verbally and in written form.

  • Strong problem-solving ability.

  • Proficient inMicrosoft Office suite.

  • Must be hands-on and must be able to meet deadlines for his or her responsibilities either directly or indirectly.


JOB SPECIFICATIONS:



  • The employee may be required to stand, walk, push, pull, reach overhead, and bend to the floor.

  • Exert up to 50 pounds of force occasionally, and/or exert up to 10 pounds of force frequently.

  • Visualacuity – Normal requirements for reading written instructions and computer screens.

  • Hearingability – Normal requirements for understanding verbal instructions.

  • Workingconditions – The employee is subject to a normal office environment with occasional exposure to high noise levels and/or physical hazards when visitingthe manufacturingfloor.

  • Capable of wearing appropriate related PPE for extended periods of time.

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