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Pharma Qa Jobs (NOW HIRING)

QA Associate

Pearl River, NY · On-site

$55K - $95K/yr

About RK Pharma RK Pharma is a pharmaceutical organization dedicated to delivering high-quality ... About the Role The QA Associate supports production-related quality activities to ensure processes ...

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Pharma Qa information

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$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.

QA Associate

Careers at RK Pharma Inc.

Pearl River, NY • On-site

$55K - $95K/yr

Full-time

Re-posted 16 days ago


Job description

Description:

About RK Pharma
RK Pharma is a pharmaceutical organization dedicated to delivering high-quality, affordable drug products through disciplined execution and strong internal collaboration. Our work is not patient-facing, but it directly supports the safety, reliability, and compliance of products relied upon downstream.

We value people who take pride in careful work, respect quality systems, and understand that consistency and sound judgment matter more than speed or spotlight.


About the Role
The QA Associate supports production-related quality activities to ensure processes, data, and documentation meet GMP and regulatory expectations. This role works closely with Microbiology, Manufacturing, and other Quality functions to help maintain a state of control across facilities and systems.

This position is well-suited for someone with a microbiology background who is detail-oriented, thoughtful, and comfortable working within structured quality systems. Success comes from steady judgment, clear communication, and the confidence to ask questions or raise concerns when something does not look right.


Requirements:

Key Responsibilities

  • Provide Quality Assurance support and oversight for microbiology-related activities, including environmental monitoring and utility monitoring
  • Review microbiology data, records, and reports for accuracy, completeness, and GMP compliance
  • Support investigations related to microbial excursions, deviations, and OOS/OOT results Assist with CAPAs, change controls, and risk assessments that impact microbiology systems
  • Ensure documentation is completed clearly, accurately, and in accordance with approved procedures
  • Participate in internal audits, inspections, and readiness activities as needed
  • Collaborate with Microbiology, Manufacturing, Validation, and broader Quality teams
  • Escalate quality concerns promptly and appropriately through established channels


What We’re Looking For


Required:

  • Bachelor’s degree in Microbiology, Biology, or a related scientific discipline Experience in a GMP-regulated pharmaceutical, biotechnology, or similar environment
  • Working knowledge of microbiology concepts such as environmental monitoring, contamination control, and aseptic practices Strong attention to detail and disciplined documentation habits
  • Ability to follow established procedures and quality systems Clear written and verbal communication skills

Preferred

  • Prior experience in Quality Assurance or QC
  • Familiarity with cleanroom operations and environmental monitoring programs
  • Experience supporting audits or regulatory inspections


How We Work

At RK Pharma, quality takes priority over speed. Procedures are followed for a reason. Questions and escalation are encouraged. Helpfulness and respect are expected across teams. No one is asked to cut corners to meet a deadline. People who do well here are steady, thoughtful, and comfortable letting the quality of their work speak for itself.


Physical and Work Environment

Requirements Ability to work in controlled environments, including cleanrooms as required

Ability to review data and documentation for extended periods Compliance with gowning, hygiene, and safety requirements


What We Offer

A stable, quality-focused work environment Clear expectations and structured onboarding Collaboration with experienced Quality professionals The opportunity to directly support product quality and compliance

Equal Opportunity Employer RK Pharma is an equal opportunity employer. We are committed to fair, consistent, and respectful hiring practices.