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Quality Assurance In Pharmaceutical Jobs (NOW HIRING)

Cipla

QA Inspector II - 2nd Shift

Fall River, MA · On-site

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. * Minimum of 3 years' experience in quality assurance in a cGMP pharmaceutical ...

Cipla

QA Inspector II - 2nd Shift

Fall River, MA

$26 - $33/hr

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. * Minimum of 3 years' experience in quality assurance in a cGMP pharmaceutical ...

Cipla

$26 - $33/hr

Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. Minimum of 3years' experience in quality assurance in a cGMP pharmaceutical ...

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing ... Quality Assurance Engineer Location: Tampa, FL - 33634 Duration: 12 months Job Type: Temporary ...

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How much do quality assurance in pharmaceutical jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality assurance in pharmaceutical in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

Is quality assurance a good career in the pharmaceutical industry?

Quality assurance in the pharmaceutical industry is a stable and growing career, focusing on ensuring products meet safety and regulatory standards. It often requires knowledge of Good Manufacturing Practices (GMP), quality control processes, and relevant certifications, making it a vital role for maintaining product integrity and compliance.

What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?

Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.

What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?

A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.

What does quality assurance do in the pharmaceutical industry?

Quality assurance professionals in the pharmaceutical industry ensure that products meet safety, quality, and regulatory standards throughout the manufacturing process. They develop and implement procedures, conduct audits, and review documentation to prevent defects and ensure compliance with Good Manufacturing Practices (GMP).

What does a quality assurance professional do in the pharmaceutical industry?

A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.

What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?

AspectQuality Assurance In PharmaceuticalQuality Control In Pharmaceutical
FocusProcesses, compliance, and preventing defectsTesting and inspecting products for defects
ResponsibilitiesDeveloping quality systems, audits, documentationSampling, testing, and analyzing products
CredentialsGMP certifications, quality management trainingLab certifications, analytical testing skills
Work EnvironmentOffice-based, quality departments, manufacturing sitesLaboratories, manufacturing facilities

Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.

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Quality Assurance In Pharmaceutical jobs near you
Infographic showing various Quality Assurance In Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Quality Assurance Associate I - 2nd Shift

Siegfried

Irvine, CA

$30 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact.

Your Role:

The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release.
2nd Shift Hours: 2 PM - 10:30 PM Monday through Friday

Your Profile:

Responsibilities

QA Production Floor Support

  • Provide Quality support to Manufacturing personnel on the shop floor for compounding and QA- in-process checks.
  • Perform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CSIT/PID test, weight check, and torque test.
  • Perform AQL and Level II Visual Inspection for Finished products.
  • Prepare in-process samples for submission to the Quality Control laboratory. Support handling of GMP events and initiation of deviation investigations.
  • Read, understand, and follow SOP's and comply with cGMP and GDP.
  • Support the issuance of GMP documentation to the Manufacturing floor.

QA Batch Review and Product Release

  • Review executed batch records for completeness, accuracy and compliance with approved procedures and Good Documentation Practices (GDP) and resolve discrepancies with manufacturing operators or supervisors.
  • Use computerized systems and software such as SAP, LIMS, and TrackWise for data collection and batch record review.
  • Enter and verify data from executed batch records into the Product Log Sheet and maintain the database up to date at all times.
  • Participate in deviation investigation and CAPA implementation.
  • Initiate Certificate of Conformance and prepare executed batch records for product release in a timely manner to meet compliance requirements and business needs.
  • Scan and file batch records (physically & electronically).
  • Assist in writing and/or revising SOPs to ensure compliance with cGMP and other applicable regulations.

Required Knowledge, Skills and Abilities

  • Working knowledge of QA principles In Pharmaceutical and/or other FDA regulated industries required
  • Good computer skills
  • Strong attention to detail
  • Good oral and written communication skills
  • Ability to work overtime and/or work
  • on weekend as needed

Required Education and Experience

  • Bachelor's Degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required
  • 1-2 years' experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required

Target Pay Range: $30-32/hour +10% Differential when working on 2nd Shift (2 PM -10:30 PM)

Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.

Your Benefits:

  • Medical, Dental, Vision, Life
  • Voluntary Accident, Hospital, Pet
  • 401K
  • Generous Time Off Structure including PTO, Holidays, Sick & Personal

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.

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