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Ipqa Jobs (NOW HIRING)

Glenmark Pharmaceuticals

IPQA Specialist

Monroe, NC · On-site

The IPQA Specialist is a member of the Manufacturing Quality Assurance department at the Monroe manufacturing facility, reporting to either IPQA Supervisor/Manager . Primary responsibilities for this ...

LGM Pharma, LLC

PRODUCTION CONTROL COORDINATOR

Irvine, CA · On-site

$24 - $30/hr

Support manufacturing on the workflow of batch records between Manufacturing, IPQA, and QA, and other departments to ensure timely movement and closure of documentation. * Review batch records for ...

T1 Energy Inc.

In-Process Quality Technician I

Dallas, TX · On-site

$17.75 - $24/hr

The Role T1 Energy is seeking a detail-oriented IPQA Tech 1 to join our Module Quality Assurance team. In this role, you will be stationed directly on the advanced manufacturing floor, serving as a ...

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Ipqa information

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$35K

$61.6K

$90K

How much do ipqa jobs pay per year?

As of Sep 9, 2026, the average yearly pay for ipqa in the United States is $61,583.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,500.00 and $79,000.00 per year, depending on experience, location, and employer.

What are IPQA roles and responsibilities?

IPQA stands for In-Process Quality Assurance. Professionals in this role are responsible for monitoring and ensuring the quality of products during the manufacturing process, particularly in the pharmaceutical and biotechnology industries. Their tasks include performing in-process checks, verifying compliance with standard operating procedures (SOPs), documenting observations, and ensuring corrective actions are taken to address deviations. IPQA officers help maintain product quality and regulatory compliance throughout the production cycle.

What skills and qualifications are needed to thrive as an IPQA professional?

To thrive as an IPQA professional, you need a solid understanding of GMP guidelines, quality control principles, and relevant scientific or pharmaceutical qualifications. Familiarity with tools such as LIMS, ERP systems, and documentation software, along with certifications like Six Sigma or ISO standards, is typically required. Attention to detail, strong communication, and problem-solving abilities are essential soft skills in this role. These competencies are critical for ensuring product quality, regulatory compliance, and smooth manufacturing processes in highly regulated industries.

What are common challenges faced by IPQA professionals in maintaining real-time compliance during production?

IPQA (In-Process Quality Assurance) professionals often encounter challenges such as rapidly changing production schedules, simultaneous monitoring of multiple lines, and ensuring all processes adhere to strict regulatory standards in real-time. Balancing thorough documentation with swift decision-making is essential, as IPQA must promptly address deviations and collaborate closely with production, quality control, and engineering teams. Staying current with evolving industry regulations and effectively communicating quality requirements to diverse stakeholders are also key aspects of the role.

What is the difference between Ipqa vs Quality Assurance Specialist?

AspectIpqaQuality Assurance Specialist
CertificationsISO 9001, GMP, HACCPISO 9001, Six Sigma, GMP
Work EnvironmentManufacturing, Food, PharmaceuticalManufacturing, Software, Healthcare
Employer & Industry UsageManufacturers, Food & Beverage, PharmaVarious industries including manufacturing and tech

Ipqa (International Product Quality Auditor) focuses on auditing and ensuring product quality compliance in manufacturing and production environments. Quality Assurance Specialist is a broader role involved in developing quality systems, procedures, and testing across multiple industries. While both roles emphasize quality standards, Ipqa is more audit and compliance-oriented, whereas Quality Assurance Specialist involves ongoing quality management and process improvement.

What is the work of IPQA?

IPQA (In-Process Quality Assurance) involves monitoring and inspecting manufacturing processes to ensure product quality and compliance with standards. It includes conducting audits, sampling, and documentation to identify and address deviations during production, often requiring knowledge of quality control tools and standards such as GMP or ISO.

What skills are needed for IPQA?

IPQA (In-Process Quality Assurance) professionals need strong attention to detail, knowledge of quality control procedures, and familiarity with manufacturing processes. Skills in inspection, documentation, and the use of quality tools like SPC or Six Sigma are also important, along with good communication and problem-solving abilities.

What cities are hiring for Ipqa jobs?

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What states have the most Ipqa jobs?

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What other helpful pages are available for Ipqa?

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Ipqa jobs near you
Infographic showing various Ipqa job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution, with an average salary of $61,583 per year, or $29.6 per hour.

IPQA Specialist

Monroe, NC • On-site

Glenmark Pharmaceuticals Inc.
See more jobs at Glenmark Pharmaceuticals Inc.external

Full-time

Posted 6 days ago

Job description

POSITION SUMMARY:

The IPQA Specialist is a member of the Manufacturing Quality Assurance department at the Monroe manufacturing facility, reporting to either IPQA Supervisor/Manager . Primary responsibilities for this position are to provide quality support and oversight while production activities are underway in preparation (e.g., line clearance, material staging, label preparation, etc.) and during manufacturing, filling, packaging, validation, etc. The IPQA Specialist reviews and compiles BPR data associated with Glenmark products, participates and assists management of the visual inspection program for the sterile injectable products, provides oversight of critical Utility operations.

OVERALL JOB RESPONSIBILITIES

  • Maintain quality system controls to ensure state of compliance and no critical and major market complaints to prevent costly recalls.
  • Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency.
  • Perform line clearance and approval for use of areas/rooms for Dispensing, Sampling, Manufacturing and Packaging.
  • Obtain and analyse utility samples as needed.
  • Perform Packaging label creation.
  • Provide Quality support during In-Process Sampling, Validation, Cleaning Verification, activities, etc.
  • Perform regularly-scheduled and as-needed Compliance walk-throughs in Production and Warehouse.
  • Maintain Retain Sample storage.
  • SME for visual inspection for vial and syringe products
  • Perform AQL visual inspection of finished good products
  • Review batch manufacturing documentation and assist Production personnel with documentation.
  • Ensure compliance with Standard Operating Procedures (SOPs), Forms, Batch Production Records, Protocols, as needed.
  • Operate in compliance of cGMP, 21CFR, USP, EP and ICH regulatory requirements.

KNOWLEDGE, SKILLS AND ABILITIES

Education

(degree / diploma)

  • Bachelor’s degree in scientific discipline or closely related technical field of study.

Experience

  • 3+ years of relevant pharmaceutical manufacturing experience
  • Experience in data review function of with previous experience on the floor in Manufacturing (Dispensing, Pouching, Inspection and Packaging, etc.) and/or Quality experience.
  • Quality experience is preferred.

Knowledge and Skills (Functional / Technical)

  • Strong Technical writing skills.
  • Knowledge of current cGMP regulations.
  • Proficient in Windows, Microsoft Word, Excel.
  • Good written, verbal, and communication skills.
  • Good documentation skills.
  • Strong organizational skills.
  • Time management

Leadership / Managerial Attributes

  • No direct or indirect reports/Individual Contributor.