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Pharma Qa Jobs (NOW HIRING)

LGM Pharma, LLC

SUPERVISOR, QUALITY ASSURANCE

Irvine, CA · On-site

$90K - $105K/yr

... Quality Assurance in a GMP facility, including people management and/or equivalent combination of ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

PCI Pharma Services

QA Associate III

San Diego, CA · On-site

$29.65 - $33.36/hr

This position performs a range of routine and semi-routine QA Raw Materials activities to ensure ... Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and ...

PCI Pharma Services

QA Associate III

San Diego, CA · On-site

$29.65 - $33.36/hr

This position performs a range of routine and semi-routine QA Raw Materials activities to ensure ... Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and ...

Actalent

QA Specialist (Cosmetics/Pharma)

Hopkins, MN

$25 - $30/hr

Quality Assurance Specialist Pharma/Cosmetics | Contract-to-hire | Long-term Growth The Quality Assurance Specialist ensures product and process quality within a GMP manufacturing environment by ...

New

Jobsbridge

Clinical QA Lead

Boston, MA · On-site

Title : Clinical QA Lead Location : Boston, MA Duration : 6+ Months 1. Minimum of 5-8 years of ... Experience in Bio pharma / Biotechnology / Clinical Research Organization. 6. Exposure to ...

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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 Aug 8, 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 is a Pharma QA?

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?

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 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:
What job categories do people searching Pharma Qa jobs look for? The top searched job categories for Pharma Qa jobs are:
Pharma Qa jobs near you
Infographic showing various Pharma Qa job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 3% Part Time, and 7% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Quality Assurance Associate

Garonit Pharmaceutical

Fairfield, NJ • On-site

Other

Re-posted 10 days ago

Job description

QA Associate
Onsite in Flanders, NJ and Fairfield, NJ

Garonit Pharma is seeking a detail-oriented and collaborative QA Associate to support daily Quality Assurance operations and uphold our Quality Management System. This role is essential in ensuring product quality, cGMP compliance, and smooth operational support across manufacturing and warehouse functions. 

What You'll Be Doing:

  • Issue, review, and maintain batch records
  • Prepare and review documentation for Operations
  • Review Certificates of Analysis (COAs)
  • Track material status and maintain data integrity
  • Author, revise, and manage SOPs and controlled documents
  • Write investigations, change controls, and implement CAPAs
  • Conduct employee training
  • Support internal, customer, and regulatory audits
  • Compile data for Annual Product Reviews (APRs)
  • Schedule calibration and certification activities
  • Respond to customer requests and questionnaires
  • Track vendor qualifications
  • Perform data entry, collection, and documentation review
  • Review shipment inspection forms
  • Assist with other QA duties as assigned

What You Bring:

  • Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline preferred
  • Minimum 1-3 years of experience in a regulated cGMP pharmaceutical manufacturing environment
  • FDA-regulated industry experience
  • Experience supporting QC systems and auditing laboratory documentation/data is strongly preferred
  • Experience with Empower software is preferred
  • Working knowledge of 21 CFR Parts 210/211 and ICH guidelines
  • Strong understanding of cGMP and Quality Management Systems
  • Experience reviewing laboratory documentation, analytical data, and quality records
  • Excellent documentation accuracy and attention to detail
  • Strong organizational, written, and verbal communication skills
  • Proficiency in Microsoft Word and Excel
  • Ability to multitask in a fast-paced environment
  • Strong interpersonal skills with the ability to work independently and collaboratively across departments

Apply