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Pharma Qc Jobs in Indiana (NOW HIRING)

Stevanato Group S.p.A.

Assembly Operator

Fishers, IN · On-site

$15.25 - $18.50/hr

For more than 70 years, we have been committed to provide integrated solutions for pharma and ... Familiarity with quality control procedures and standards. * Basic knowledge of safety regulations ...

Danaher

Supplier Quality Engineer

Indianapolis, IN

The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... pharma, with strong knowledge of supplier qualification, audits, change control, CAPA/RCA, QMS ...

Danaher

Supplier Quality Engineer

Indianapolis, IN · On-site

The Supplier Quality Engineer is responsible for driving supplier quality performance, leading ... pharma, with strong knowledge of supplier qualification, audits, change control, CAPA/RCA, QMS ...

CYNET SYSTEMS

Operations Quality Principal

Indianapolis, IN · On-site

$64 - $67/hr

Experience working within a highly regulated manufacturing environment (such as Pharma, Diagnostics ... Establish and champion clean repository management, version control, and collaborative code review ...

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Pharma Qc information

What is the difference between Pharma Qc vs Pharma Quality Assurance (QA)?

AspectPharma QcPharma QA
CertificationsGMP, GMP-related trainingGMP, GMP-related training
Work EnvironmentLaboratory testing, sample analysisProcess audits, documentation review
ResponsibilitiesTesting raw materials, in-process, finished productsDeveloping, implementing quality systems, audits
Industry UsageQuality control testing in manufacturingEnsuring compliance, process quality assurance

Pharma Qc and Pharma QA roles both focus on quality in pharmaceutical manufacturing but differ in scope. Pharma Qc primarily involves laboratory testing and sample analysis to ensure product quality, while Pharma QA emphasizes process oversight, audits, and compliance systems. Both roles require GMP knowledge and are essential for maintaining industry standards.

What are popular job titles related to Pharma Qc jobs in Indiana?

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

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

The top searched job categories for Pharma Qc jobs in Indiana are:

Pharma Qc jobs near you
Infographic showing various Pharma Qc job openings in Indiana as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Senior CSV Validation Specialist (Building Management Systems)

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 13 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