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Pharmaceutical Quality Control Manager Jobs in Indiana

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

Responsibilities include analyst training, performance management, conflict resolution, laboratory ... Experience * At least 5 years of experience in pharmaceutical quality control, analytical ...

IMI

Aggregate Quality Control Technician

Noblesville, IN · On-site

$17.50 - $22.50/hr

Perform testing procedures and report those results to the QC Manager * Demonstrate a commitment to communicating, improving, and adhering to safety policies in all work environments * Maintain ...

Pkaza

QA/QC Engineer Data Center Construction

Chesterton, IN · On-site

$79K - $105K/yr

Data Center Construction QA / QC Manager - Chesterton, IN This opportunity is with an established General Contractor that specializes in converting existing Buildings and Structures into complex ...

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Pharmaceutical Quality Control Manager information

See Indiana salary details

$29K

$77.4K

$123.2K

How much do pharmaceutical quality control manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for pharmaceutical quality control manager in Indiana is $77,384.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,600.00 and $95,200.00 per year, depending on experience, location, and employer.

What does a pharmaceutical quality control manager do?

A Pharmaceutical Quality Control Manager oversees the testing and quality assurance processes involved in manufacturing pharmaceutical products. They ensure that all products meet regulatory standards and company specifications for safety, efficacy, and quality. This role includes supervising laboratory staff, developing and implementing quality control procedures, and maintaining compliance with government regulations such as Good Manufacturing Practices (GMP). They also analyze data, investigate quality issues, and work closely with other departments to resolve any problems. The ultimate goal is to ensure that patients receive safe and effective medications.

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

To thrive as a Pharmaceutical Quality Control Manager, you need a strong background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant degree and experience in quality assurance. Familiarity with analytical instruments (e.g., HPLC, GC), quality management systems, and regulatory standards like GMP or FDA guidelines is typically required. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring compliance. These skills ensure product safety, regulatory adherence, and efficient team operations in a highly regulated industry.

What are some common challenges faced by pharmaceutical quality control managers in ensuring compliance with regulatory standards?

Pharmaceutical Quality Control Managers often face the challenge of staying current with evolving regulatory requirements from agencies such as the FDA or EMA. They must ensure all laboratory processes, documentation, and product testing meet strict guidelines, which can be complicated by new technologies or changing manufacturing practices. Another challenge is managing cross-functional communication between production, R&D, and regulatory affairs to promptly address quality issues. Successfully navigating these challenges requires a keen eye for detail, strong leadership, and ongoing professional development.

What is the difference between Pharmaceutical Quality Control Manager vs Pharmaceutical Quality Assurance Specialist?

AspectPharmaceutical Quality Control ManagerPharmaceutical Quality Assurance Specialist
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; certifications like CQE or GMP training are commonSimilar credentials; often holds degrees in life sciences and certifications in GMP and QA practices
Work EnvironmentOversees laboratory testing, quality control labs, and production environmentsFocuses on developing, implementing, and auditing quality assurance systems across production
Employer & Industry UsageUsed in pharmaceutical manufacturing, biotech, and related industriesCommonly employed in pharmaceutical companies, ensuring compliance and process quality

While both roles require similar educational backgrounds and certifications, the Pharmaceutical Quality Control Manager primarily manages laboratory testing and quality control processes, whereas the Pharmaceutical Quality Assurance Specialist focuses on establishing and maintaining quality systems and compliance. Both are essential for ensuring product safety and efficacy in the pharmaceutical industry.

Is pharmaceutical quality control management a good career?

Pharmaceutical quality control management is a stable and important career in the healthcare industry, focusing on ensuring product safety and compliance with regulations. It typically requires knowledge of Good Manufacturing Practices (GMP), laboratory skills, and certifications such as a degree in pharmacy, chemistry, or related fields. The role offers opportunities for advancement and job stability due to the critical nature of quality assurance in pharmaceuticals.

What are the most commonly searched types of Pharmaceutical Quality Control jobs in Indiana?

The most popular types of Pharmaceutical Quality Control jobs in Indiana are:

What are popular job titles related to Pharmaceutical Quality Control Manager jobs in Indiana?

For Pharmaceutical Quality Control Manager jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Quality Control Manager jobs in Indiana look for?

The top searched job categories for Pharmaceutical Quality Control Manager jobs in Indiana are:

What cities in Indiana are hiring for Pharmaceutical Quality Control Manager jobs?

Cities in Indiana with the most Pharmaceutical Quality Control Manager job openings:

Pharmaceutical Quality Control Manager jobs near you
Infographic showing various Pharmaceutical Quality Control Manager job openings in Indiana as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $77,384 per year, or $37.2 per hour.

Quality Control Supervisor

Orano

Brownsburg, IN • On-site

Full-time

Posted 23 days ago

Job description

Description
Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells.
With a solid portfolio of development projects covering a diverse range of biological molecules capable of recognizing and targeting various forms of cancerous tumors, and a reliable supply chain for Pb-212, Orano Med aims to become a leader in targeted alpha therapies, in particular addressing needs of patients currently without effective therapeutic solutions among the existing approaches.
Position Summary
This is a working supervisor role. The individual is expected to learn, remain proficient in, and provide hands-on support for all assigned test methods, laboratory processes, and documentation practices. The Supervisor will set daily priorities, maintain a strong laboratory presence, and make timely operational and technical decisions.
The Supervisor will serve as a technical subject-matter expert and people leader. Responsibilities include analyst training, performance management, conflict resolution, laboratory investigations, and cross-functional communication. Success requires sound scientific judgment, strong technical writing and verbal communication, and calm decision-making under time-sensitive conditions.
Setup & Development Phase
  • Learn, perform, and maintain proficiency in all analytical test methods, laboratory processes, and controlled documentation practices within the assigned area.
  • Support analytical method development, optimization, qualification, validation, transfer, and lifecycle activities.
  • Establish training plans, qualification requirements, testing workflows, and clear expectations for compliant laboratory execution.
  • Support laboratory commissioning, instrument qualification, method readiness, staffing readiness, and analyst training.
  • Author and review protocols, reports, standard operating procedures, specifications, investigations, and other technical documents.
  • Provide scientific and operational input during process development, technology transfer, validation, and regulatory submission activities.

Production Phase
Top Priority: Execute and supervise QC testing for batch release within hours of production
Routine Functions - QC
  • Direct daily QC Chemistry laboratory operations, assign work, balance staffing, and ensure testing priorities are clearly understood.
  • Maintain hands-on capability and perform or directly support routine test methods when needed to protect testing timelines and product release.
  • Serve as the primary technical subject-matter expert for analytical methods, laboratory investigations, and complex technical issues.
  • Make timely laboratory decisions during testing and release, escalating significant quality, safety, or compliance risks appropriately.
  • Coordinate testing priorities with Manufacturing, Quality Assurance, Supply Chain, and other functions to meet production schedules.
  • Train, coach, and evaluate laboratory personnel; provide clear feedback, reinforce accountability, and resolve personnel conflicts promptly and fairly.
  • Maintain a visible leadership presence in the laboratory during critical testing, troubleshooting, and release operations.
  • Review analytical data, laboratory records, calculations, and results for accuracy, completeness, scientific validity, and compliance.
  • Lead laboratory investigations and corrective actions, and support inspections, audits, deviations, change controls, and CAPA activities.

Continuous Improvement
  • Evaluate method performance, laboratory trends, deviations, recurring issues, and workload data to identify improvement opportunities.
  • Lead root-cause analysis and ensure corrective actions address technical, procedural, and organizational causes.
  • Improve laboratory workflows, training systems, documentation quality, and inspection readiness while maintaining cGMP compliance.
  • Promote knowledge sharing, technical development, effective communication, and cross-functional collaboration.

Location: On-site 100%
This position may receive other responsibilities as needed.
Requirements
Qualifications
Education
Bachelor's degree in chemistry, analytical chemistry, pharmaceutical sciences, radiochemistry, or a related scientific discipline is required. A Master's degree is preferred.
Experience
  • At least 5 years of experience in pharmaceutical quality control, analytical development, or a related GMP laboratory function.
  • At least 1 year of experience as a laboratory supervisor, team lead, or technical lead with responsibility for directing personnel and work.
  • Direct experience supporting radiopharmaceutical drug testing is strongly preferred.
  • Strong knowledge of analytical method execution, qualification, validation, transfer, troubleshooting, and lifecycle management.
  • Experience in a GMP-regulated environment supporting clinical or commercial manufacturing.
  • Hands-on experience with techniques such as HPLC, GC, gamma spectroscopy, radio-TLC, dose calibrators, and related instrumentation.
  • Demonstrated technical writing, verbal communication, decision-making, coaching, and personnel conflict-resolution skills.

Skills
  • Strong laboratory presence, safety awareness, and hands-on technical leadership
  • Technical subject-matter expertise, scientific troubleshooting, and data review
  • Sound decision-making under time-critical conditions
  • Clear technical writing and effective verbal communication

  • Coaching, performance feedback, accountability, and personnel conflict resolution
  • Organization, prioritization, attention to detail, and urgency while maintaining cGMP standards

Other
  • Travel <10>
  • Lift 50 lbs.

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