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Pharmaceutical Quality Control Manager Jobs in Indiana

Autocar, LLC

Quality Manager (QA/QC)

Hagerstown, IN · On-site

Quality Manager (QA/QC) Location: Hagerstown, IN Company: Autocar Drive Quality. Lead Excellence. Make an Impact. At Autocar, quality isn't just a checkpoint, it's a commitment. We're looking for a ...

Novartis

Supervisor, QC Chemistry

Indianapolis, IN · On-site

$88K - $132K/yr

In this people management role, the QC Chemistry Supervisor works with the Quality Control team in ... Minimum of 5 years of relevant experience in the pharmaceutical, biologics, medical device, or ...

UFP Industries

Quality Control

Nappanee, IN · On-site

Job Summary The Quality Control Inspector is responsible for the measurement and visual inspection ... Stops production and/or other operations and notifies proper personnel and management upon ...

UFP Industries

Quality Control

Nappanee, IN · On-site

Job Summary The Quality Control Inspector is responsible for the measurement and visual inspection ... Stops production and/or other operations and notifies proper personnel and management upon ...

Tate & Lyle

QC Lab Supervisor

Lafayette, IN · On-site

$71K - $95K/yr

Manage laboratory inventory and maintain adequate supplies to support operations. * Coordinate ... Experience in food, beverage, ingredient, pharmaceutical, or other regulated manufacturing ...

Tate & Lyle

QC Lab Supervisor

Lafayette, IN · On-site

$71K - $95K/yr

Manage laboratory inventory and maintain adequate supplies to support operations. * Coordinate ... Experience in food, beverage, ingredient, pharmaceutical, or other regulated manufacturing ...

True Rx

Quality Control Specialist

Washington, IN · On-site

Quality Control Specialist Wanted at True Rx Health Strategists! Are you passionate about ensuring ... Our team of pharmacists and strategists delivers proven programs that find maximum savings and ...

Faith Technologies

QC Electrician

Lebanon, IN · On-site

The Quality Control Electrician is responsible for delivery of quality control services including ... Provides guidance to field employees, project supervisors, and management on matters concerning job ...

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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.

Traveling Quality Control Manager - Self Perform Concrete

Turner Construction

Indianapolis, IN • On-site

Full-time

Re-posted 10 days ago

Turner Construction rating

7.5

Company rating: 7.5 out of 10

Based on 69 frontline employees who took The Breakroom Quiz

27th of 80 rated construction

Job description

Position Description:Manage, plan, coordinate, and develop AISC/ASME Shop Quality Control (QC) Plan. Implement policies and procedures necessary to support project schedule and deliver a fully compliant project. Manage and implement AISC/ASME Quality Manuals.

Essential Duties & Key Responsibilities:

  • Manage development and implementation of AISC/ASME Quality Control (QC) Plan in coordination with project team, owner/architect team and related code requirements .
  • Perform/manage Engineering responsibilities for AISC and ASME Quality Manual including material tracking and traceability, weld inspections, weld tracking, Non-Destructive Examination (NDE) Testing, weld procedures, weld testing, testing procedures, testing inspections, and non-conformance documentation.
  • Establish and maintain collaborative working relationships with owners, architects, consultants, subcontractors, and vendors to ensure fully compliant project.
  • Create structure and supportive environment to develop high performing team, provide professional development opportunities, and engage in coaching and mentoring relationships.
  • Manage direct reports, deliver timely performance feedback and contribute to performance appraisals during annual performance cycle, utilizing talent management systems.
  • Manage implementation of AISC/ASME Quality Manuals in collaboration with MEP Business Line SPO department and manage updates and revisions of manuals.
  • Develop comprehensive working knowledge and understanding of project-specific contract documents (including Turner's contract, plans, specifications and applicable codes).
  • Execute project-specific QC Plan in a manner that engages all project staff, subcontractors, vendors and consultants for compliance and consistent execution.
  • Plan, chair, and participate in AISC management review.
  • Perform/manage daily quality follow-up inspections on-site as required
  • Arrange for third party testing and inspections; analyze and report results and communicate with project stakeholders as appropriate.
  • Chair or attend First Work In Place (WIP) Observation with project team.
  • Knowledgeable of project-specific engineering procedures, including document control, submissions management, creation and tracking of Requests for Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
  • Contribute to project safety plan for Trades Pre-Task Plan (PTP) as related to specific inspections.
  • Understand project execution plan to manage and direct QC activities at appropriate stages of work, in line with and in support of project schedule.
  • Continually improve and apply strategies and tools to efficiently and effectively document, track, and record compliance with contract documents.
  • Expand development of QC plan as project progresses to improve quality procedures.
  • Document non-compliant materials and/or workmanship and direct team to engage with trade partners for removal and replacement of defective work. Document compliance after corrective work is completed and prior to starting any subsequent work.
  • Ensure completion of project closeout documentation and quality reports.
  • Other activities, duties, and responsibilities as assigned.

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About Turner Construction

Sourced by ZipRecruiter

Turner Construction, headquartered in New York, NY, US, is a recognized leader in the construction industry. It was established in 1902 and has since curved its niche as one of the most reputable construction firms. Turner Construction provides a broad range of services like general contracting, construction management, design-build, and consulting. Devoted to environment-friendly building practices, it is considered a pioneer in green building and sustainability efforts. Their top-tier projects include Madison Square Garden, Yankee Stadium, and the United Nations Secretariat Building in New York City. The company's mission is to deliver an exceptional product by relentless commitment to their core principles – teamwork, integrity, commitment, and community.

Industry

Construction

Company size

10,000+ Employees

Headquarters location

New York, NY, US

Year founded

1902

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