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Pharma Qc Jobs in Indiana (NOW HIRING)

ATS Automation

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

Pharma - aseptic handling and filling of liquid and powder APIs, dispensing custom R&D isolators ... Plan and document control activities and inspections * Other duties as required. Qualifications ...

Amcor plc

Quality Manager III

Terre Haute, IN · On-site

... Control (SPC) methodology to improve the acceptance of our products by our customers. In addition ... Pharma etc.) applicable to industry. * Conducts advanced statistical analysis and process ...

Amcor

Quality Manager III

Terre Haute, IN

... Control (SPC) methodology to improve the acceptance of our products by our customers. In addition ... Pharma etc.) applicable to industry. * Conducts advanced statistical analysis and process ...

Stevanato Group S.p.A.

Molding Operator

Fishers, IN · On-site

$15.25 - $18.25/hr

For more than 70 years, we have been committed to provide integrated solutions for pharma and ... Collaboration with quality control and maintenance teams is essential to troubleshoot issues and ...

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

... quality control, analytical testing, sample management, and laboratory data handling. The CSV ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

PM Group

CSV Engineer I

Indianapolis, IN

$68K - $88K/yr

... quality control, analytical testing, sample management, and laboratory data handling. The CSV ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

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All JobsPharma Qc JobsPharma Qc Jobs in Indiana

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.

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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?

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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.

QA TECHNICIAN 1 (5646)

NICE-PAK PRODUCTS LLC

Mooresville, IN

$20.24/hr

Full-time

Posted 21 days ago

Job description

POSITION PURPOSE

The Product Release Coordinator (PRC) is responsible for coordinating and executing the release of cosmetic, OTC-regulated, and EPA regulated finished products, ensuring compliance with Good Manufacturing Practices (GMP), FDA regulations, and company quality standards. This position reviews batch records including digital data in the Laboratory Information Management System (LIMS) and Shop Floor Control system, collaborates with the Quality Assurance and Manufacturing teams, and prepares Certificates of Analysis (CoAs) and other release documentation as necessary.  This individual also ensures all concerns identified during the data review are properly addressed and documented.  Once the review is complete, the PRC performs the necessary release transactions for each manufacturing lot in the electronic Warehouse Management System(s).  The PRC is responsible for coordinating release activities with the shipping and customer service teams to ensure timely disposition and communication on product availability.  The coordinator is a key link in the safe and compliant release of products, supporting the company’s commitment to consumer safety and regulatory compliance

ESSENTIAL FUNCTIONS AND BASIC DUTIES

  • Batch Review & Product Release
    • Review and approve batch records, packaging documentation, and test results for completeness, accuracy and compliance to specifications prior to product release.
    • Ensure all documentation complies with FDA, cGMP, and internal requirements.
  • Documentation & Certificate Preparation
    • Prepare and sign Certificates of Analysis for released product lots, ensuring accuracy and regulatory compliance.
    • Maintain a repository of release records and related documentation.
    • Maintain Product Release SOP and other SOP’s as necessary
  • Cross-Functional Coordination
    • Collaborate with Manufacturing, Quality Control, and Regulatory Affairs to resolve release-related issues.
    • Participate in investigations, CAPA (Corrective and Preventive Action), and non-conformance management as needed.
  • Communication
    • Communicate release status and critical quality information to internal stakeholders.
    • Liaise with customers and vendors regarding product status if necessary.
  • Return Material Authorization (RMA)
    • Manage verification of returned products for disposition and compliance action.
  • Audit Support
    • Support regulatory, customer, and internal audits related to product release documentation and processes.
  • Training
    • Responsible for training other team members to perform necessary duties to back-up the PRC role when necessary
  • Continuous Improvement
    • Recommend improvements to documentation practices and release procedures for enhanced compliance and efficiency.
    • Assist in training and implementation of new release procedures.

QUALIFICATIONS

EDUCATION/CERTIFICATION:

High School Diploma or equivalent

REQUIRED KNOWLEDGE:

Familiarity with cGMP, FDA, and OTC-specific regulatory standards.

Proficiency with documentation, batch record review, and release procedures.

Familiarity with manufacturing processes related to consumer goods.

EXPERIENCE REQUIRED:

Experience in an FDA regulated manufacturing environment (OTC, Pharma, Medical Device, Cosmetic, or Food) is preferred.

SKILLS/ABILITIES:

Strong attention to detail and organizational skills.

Excellent written and verbal communication skills for cross-team coordination.

Ability to interpret quality and regulatory documentation and standards.

Proficiency with Microsoft Office Suite and electronic Quality Management Systems (eQMS) preferred.

Analytical and problem-solving abilities in a fast-paced, regulated environment.

Proficient computer skills to support enterprise resource planning (ERP) (such as Red Prairie, SAP, AS400, Dynamic 365, Oracle) and electronic Quality Management Systems (such as Intelex, MasterControl, Harford, LIMS, Labware, Specright).   

WORKING CONDITIONS

NONE:

No hazardous or significantly unpleasant conditions.

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