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Quality Control Pharma Jobs in Indiana (NOW HIRING)

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

Develop/revise worksheets and system documentation Required Skills: * 8-10 years in Pharma/GMP environment * QC lab experience with LIMS/ELN (data admin or power user) * Strong understanding of data ...

Stark Pharma Solutions Inc

Quality Engineer

Lafayette, IN · On-site

$69K - $89K/yr

Hi, My name is Karthik Mutyala and I'm a Recruitment Manager with Stark Pharma, specializing in ... Control Plans (CP) * Conduct root cause analysis and implement corrective and preventive actions

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.

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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.

New

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 ...

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 ...

Bilfinger

$23.50 - $31.50/hr

... Pharma und Öl & Gas. Wir sind Ihr Spezialist für Industriegerüstbau, Korrosionsschutz und Isoliertechnik. Mit unseren hoch qualifizierten Teams begleiten wir den gesamten Lebenszyklus ...

Bilfinger

$23.50 - $31.50/hr

... Pharma und Öl & Gas. Wir sind Ihr Spezialist für Industriegerüstbau, Korrosionsschutz und Isoliertechnik. Mit unseren hoch qualifizierten Teams begleiten wir den gesamten Lebenszyklus ...

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.

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Quality Control Pharma information

Is quality control pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It offers stable employment, opportunities for advancement, and requires attention to detail, knowledge of laboratory techniques, and often certifications such as GMP training.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What is the role of quality control in pharma?

The role of quality control in pharma involves testing and inspecting raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and follow Good Manufacturing Practices (GMP) to identify and prevent defects, supporting regulatory compliance and product consistency.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
What are popular job titles related to Quality Control Pharma jobs in Indiana? For Quality Control Pharma jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Quality Control Pharma jobs in Indiana look for? The top searched job categories for Quality Control Pharma jobs in Indiana are:
Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

QC Analyst

Intellectt INC

Lebanon, IN • On-site

$23 - $31/hr

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a QC Analyst – Master Data (LIMS) based in Lebanon, IN with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Job Title: QC Analyst – Master Data (LIMS)
Location: Lebanon, IN (100% Onsite)
Duration: 12–18 Months
Start Date: 4/13 or 4/20

Role Overview:
Support QC data management, sample/result tracking, and development of Electronic Lab Notebook (ELN) templates. Ensure smooth LIMS operations, data integrity, and lab documentation compliance.

Key Responsibilities:

  • Manage QC data, sampling plans, and result tracking
  • Create and maintain ELN templates and master data
  • Support LIMS functionality and data verification
  • Maintain lab documentation and improve QA processes
  • Develop/revise worksheets and system documentation

Required Skills:

  • 8–10 years in Pharma/GMP environment
  • QC lab experience with LIMS/ELN (data admin or power user)
  • Strong understanding of data integrity (ALCOA+)
  • Experience with COAs, stability reports, SOPs
  • Good technical writing and communication skills

Preferred:

  • Experience in ATMP/Gene Therapy
  • Process improvement experience
  • Knowledge of ERP, MES, MODA, and LIMS interfaces
  • Strong analytical and problem-solving skills
  • Bachelor’s degree preferred
 

Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999- Ext: 225