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Pharma Qa Jobs (NOW HIRING)

MANAGER, QUALITY ASSURANCE

Taylor, MS ยท On-site

$95K - $110K/yr

Prepare QA reports and provide data to support cross-functional business needs * Oversee management ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

NC ยท On-site

$40/hr

GMP Quality Assurance Duration: 06/29/2026--- 04/04/2027 with possible extension Office: Research Triangle Park, NC 27709 Pay rate: $40/hr. on W2 * The QA Contractor, GMP Quality Assurance, reporting ...

Stokes Pharmacy (503A pharmacy), Epicur Pharma (503B facility) and STEP labs. The these divisions ... Job Title Quality Assurance Analyst FLSA Status Non-exempt Salary Starting at $20/hour based on ...

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Pharma Qa information

See salary details

$15

$44

$64

How much do pharma qa jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for pharma qa in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is the difference between Pharma Qa vs Pharma Quality Control Analyst?

AspectPharma QaPharma Quality Control Analyst
CertificationsGMP, GDP, QA certificationsGMP, QC certifications, Lab training
Work EnvironmentQuality assurance departments, documentation reviewLaboratories, testing and analysis
Employer & Industry UsagePharmaceutical companies, regulatory agenciesPharmaceutical manufacturing, testing labs

Pharma Qa professionals focus on ensuring compliance, reviewing documentation, and maintaining quality systems, while Pharma Quality Control Analysts perform laboratory testing and analysis to verify product quality. Both roles are essential in pharma manufacturing but differ mainly in scope and daily tasks.

What are Pharma QA professionals?

Pharma QA professionals, or pharmaceutical quality assurance specialists, are responsible for ensuring that pharmaceutical products and manufacturing processes meet established quality standards and regulatory requirements. They develop and implement quality management systems, conduct audits, review documentation, and oversee compliance with Good Manufacturing Practices (GMP). Their work helps ensure the safety, efficacy, and consistency of medicines before they reach patients.

What are the key skills and qualifications needed to thrive as a Pharma QA professional, and why are they important?

To thrive as a Pharma QA professional, you need a solid understanding of pharmaceutical regulations, quality assurance principles, and a relevant degree such as pharmacy, chemistry, or life sciences. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and tools like LIMS or CAPA software is typically required. Strong attention to detail, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure product safety, regulatory compliance, and the maintenance of high-quality standards in pharmaceutical manufacturing.

What are some typical challenges faced by Pharma QA professionals when ensuring regulatory compliance?

Pharma QA professionals often encounter challenges related to evolving regulatory requirements, documentation accuracy, and maintaining consistent quality across diverse manufacturing processes. Keeping up-to-date with changes from agencies like the FDA or EMA requires ongoing learning and adaptability. Additionally, QA teams must collaborate closely with production, R&D, and regulatory affairs to resolve discrepancies and implement corrective actions efficiently. Balancing thorough compliance with operational timelines and resource constraints is a common aspect of the role.
More about Pharma Qa jobs
What cities are hiring for Pharma Qa jobs? Cities with the most Pharma Qa job openings:
What states have the most Pharma Qa jobs? States with the most job openings for Pharma Qa jobs include:
Infographic showing various Pharma Qa job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 93% Full Time, 2% Part Time, 1% Temporary, and 3% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.
MANAGER, QUALITY ASSURANCE

MANAGER, QUALITY ASSURANCE

LGM Pharma, LLC

Taylor, MS โ€ข On-site

$95K - $110K/yr

Full-time

Re-posted 2 days ago


Job description

RESPONSIBILITIES:
  • Supervise daily warehouse operations to ensure efficient material flow and timely completion of Quality Assurance activities
  • Provide oversight of quality systems, including labeling, GMP training, compliance, document control, information tracking, and equipment calibration
  • Lead investigation activities, perform root cause analysis, and develop corrective and preventive action (CAPA) plans
  • Support internal and external audits and regulatory inspections, ensuring timely resolution and closure of findings
  • Develop, maintain, and control document storage and retrieval systems in compliance with GMP requirements
  • Review and approve Quality Operations processes, SOPs, and GMP documentation, as applicable
  • Utilize statistical process control to analyze quality trends and prepare KPI reports for senior management
  • Ensure timely closure and effective management of audit findings
  • Prepare QA reports and provide data to support cross-functional business needs
  • Oversee management of deviations, CAPAs, and change controls in a timely and compliant manner
  • Support customer complaint investigations, ensuring appropriate documentation and resolution
  • Supervise, train, and mentor junior QA staff to support team development and capability building
  • Ensure full compliance with cGMP regulations and all applicable SOPs
  • Experience in Active Pharmaceutical Ingredient (API) environments
  • Experience in quality operations within manufacturing, warehouse, and supply chain environments
  • Exposure to international supply chain and distribution operations preferred
  • Strong knowledge of Quality Systems and GMP compliance requirements
  • Hands-on experience with vendor management, customer complaints, deviations, CAPA, change control, and investigations
  • Experience supporting internal and external audits and regulatory inspections
  • Knowledge of document control systems, GMP training programs, labeling systems, and metrology programs
QUALIFICATIONS:
  • Bachelorโ€™s degree in a scientific discipline
  • 10+ years of experience in Quality Assurance within a GMP-regulated manufacturing environment, or equivalent combination of education and experience
  • 5+ years of experience in a supervisory or leadership role within a GMP-regulated manufacturing or distribution environment preferred
  • Ability to read and interpret technical procedures, SOPs, GMP regulations, and governmental requirements
  • Strong written and verbal communication skills
  • Ability to organize, prioritize, and manage multiple tasks with minimal supervision
  • High attention to detail and strong analytical skills
  • Knowledge of ICH Q7, 21 CFR Part 11, and 21 CFR 210 & 211
  • ASQ certifications, ISO 9000 knowledge, or formal audit training preferred.

At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer.

All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.