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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

$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 ...

Jobsbridge

Clinical QA Lead

Boston, MA

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 Jul 18, 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:
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 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.
Incoming Quality Assurance Technician Mid Shift

Incoming Quality Assurance Technician Mid Shift

QuVa Pharma

Sugar Land, TX

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago

QuVa Pharma rating

6.9

Company rating: 6.9 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

65th of 74 rated pharmaceutical

Job description

The Incoming Quality Assurance Technician position contributes to the organization through coordinating Incoming Quality Assurance (IQA) aspects of raw materials and sterile supplies for compounding pharmaceuticals as well as perform preprinted label receipt inspections and quality processes. This role requires critical thinking and authority to proactively address and/or escalate IQA issues. The Incoming Quality Assurance Technician performs basic QA functions related to verification of incoming materials. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full-time role for our Mid shift, working Monday through Friday from 10 AM - 7 PM CST. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land, TX location.  This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What Incoming Quality Assurance Technician Each Day:

  • QC Test steps in ERP system
  • Inspection of bulk bags from other Quva sites
  • Assist with the Coordination of transfers between Quva Sites
  • Incoming Environmental plate sampling or sending for testing
  • Quality inspection and QC step in ERP of labels
  • Quality inspections/sampling verification raw materials, sterile supplies
  • Quality review / verification of critical information related to the receipt of incoming materials
  • Escalate any discrepancies or non-conformances found during incoming receipt inspection
  • Retrieves / requests quality documents (CoA, CoC, CoS...) from vendors for incoming materials
  • Ensures compliance of incoming materials prior to use in Manufacturing Operations
  • Ensures company compliance to Quva Pharma’s Standard Operating Procedures (SOPs) and Quality Management System (QMS)
  • Follows all regulatory guidelines, cGMP guidelines as required by the job function
  • Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs
  • Performs visual inspections of products to verify conformance to quality, safety, and regulatory standards
  • Other duties as designated by Quality Management

Our Most Successful Incoming Quality Assurance Technician:

  • Understands updating Standard Operating Procedure, with documentation of summary of changes and version control
  • Manages projects coordinating cross-departmental activities
  • Is proficient in Microsoft Office, Adobe, Word and Excel
  • Is detail-oriented and has strong verbal and written communications skills

Minimum Requirements for this Role:

  • A High School diploma or equivalent
  • At least 2 years’ experience in FDA regulated Quality Assurance, Sterile Compounding and/or GMP production facility
  • 18+ years of age
  • Will be required to undergo a color perception exam and must be able to produce a passing test result
  • Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction
  • Able to successfully complete a drug and background check
  • Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas

Any of the Following Will Give You an Edge:

  • Bachelor’s Degree in life science or equivalent work experience

Benefits of Working at Quva:

  • Set, full-time, consistent work schedule
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 17 paid days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industry-leading high growth company with future career advancement opportunities

About Quva:

Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva’s overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.

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