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Ipqa Jobs (NOW HIRING)

SAFE HARBOR MARINAS

Service Coordinator

West Palm Beach, FL · On-site

$19 - $24.25/hr

Administrative Support: • Review, process, and maintain accurate records of IPQA forms. • Organize and order general office supplies to ensure the smooth functioning of the office. • Organize ...

Safe Harbor Marinas

Service Coordinator

West Palm Beach, FL · On-site

$19 - $24.25/hr

Review, process, and maintain accurate records of IPQA forms. Organize and order general office supplies to ensure the smooth functioning of the office. Organize and prepare for routine and periodic ...

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$35K

$61.6K

$90K

How much do ipqa jobs pay per year?

As of Sep 11, 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?

Cities with the most Ipqa job openings:

What states have the most Ipqa jobs?

States with the most job openings for Ipqa jobs include:

What job categories do people searching Ipqa jobs look for?

The top searched job categories for Ipqa jobs are:

What other helpful pages are available for Ipqa?

Other pages related to Ipqa:

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.

Compression Operator I - Day Shift

Brookhaven, NY • On-site

Amneal Pharmaceuticals LLC
Pharmaceutical and Medicine Manufacturing • 5 - 10K employees
Learn more about Amneal Pharmaceuticals LLCexternal

$17.50 - $23.50/hr

Full-time

Medical, Retirement

Re-posted 3 days ago

Amneal Pharmaceuticals rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

Description:

This entry-level role in the Compression Department is responsible for the setup and operation of compression machinery in accordance with company Standard Operating Procedures (SOPs). The Compression Operator ensures full compliance with cGMP standards to support the production of high-quality pharmaceutical products.

Schedule:

1st Shift 7:00am - 3:30pm Monday to Friday


Essential Functions:

  • Responsible for conducting in-process checks including average weight, thickness, hardness, friability, and individual tablet weight, among others.
  • Initiates 'B' and 'A' level cleaning of compression rooms and ensures compliance with the In-Process Quality Assurance (IPQA) procedures.
  • Accurately identifies and segregates rejected blends and tablets, ensures required quality checks are completed, and upholds cleanliness and organization of the compression room and equipment to maintain compliance and operational efficiency.
  • Promptly notifies the Supervisor of any machine abnormalities or expired calibration status. Ensures weighing scales are kept clean and orderly for accurate calibration checks.
  • Verifies ingredients weighed in Mixing & Granulation against entries in the Production Batch Record (PBR), reporting any discrepancies to the Supervisor or designee. Responsible for real-time documentation across all Compression operations and for reviewing batch records to ensure accuracy.

Additional Responsibilities:

  • Other duties as assigned.
  • Flexible to work extended hours when required.

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws. 


Education:

  • High School or GED General HS Curriculum - Preferred

Experience:

  • 1 year or more in Experience in Pharmaceutical Manufacturing Environment

Skills:

  • Ability to read, write, and communicate in English. - Intermediate
  • High school level math and mechanical skills. - Intermediate
  • Ability to work as part of a team. - Intermediate
  • Attention to detail and accuracy. - Intermediate
  • Basic computer literacy with the ability to use web browsers, typing applications, Microsoft Office, and related communication tools. - Intermediate
  • May be required to lift up to 50 lbs.

Specialized Knowledge:

  • High speed Compression Machine set up preferred.

APPLICATION PROCESS:

  1. If you are selected for screening, you will receive an email or text containing a Calendly link to schedule your 15-minute screening call with the Recruiter
  2. Clicking on the Calendly link will take you to a calendar page that shows options for dates / times and you select what works for you
  3. The Recruiter will call you at the appointed date /time and complete the telephone screening with you
  4. Please check your email / texts accordingly

Additional Requirement: This position requires successful completion of an OSHA-compliant Respirator Fit Test.

The hourly base salary for this position ranges from $17.50 to $23.50 per hour.   Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting.  Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills.  At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement.  We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.

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