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Quality Assurance In Pharmaceutical Jobs (NOW HIRING)

Cipla

QA Inspector I - 3rd Shift

Fall River, MA · On-site

$21 - $26/hr

Job Title : QA Manufacturing Inspector - On-the-floor Inspector FLSA Classification : Full-Time, ... Advanced vocational training or education in pharmaceutical manufacturing, industrial management or ...

Cipla

QA Inspector I - 3rd Shift

Fall River, MA · On-site

$21 - $26/hr

Job Title : QA Manufacturing Inspector - On-the-floor Inspector FLSA Classification : Full-Time, ... Advanced vocational training or education in pharmaceutical manufacturing, industrial management or ...

Cipla

$21 - $26/hr

Job Title : QA Manufacturing Inspector - On-the-floor Inspector FLSA Classification : Full-Time, ... Advanced vocational training or education in pharmaceutical manufacturing, industrial management or ...

Pinnaql

QA Validation Specialist

Sanford, NC · On-site

Minimum 5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments. * Strong experience supporting equipment qualification from a Quality Assurance perspective.

Pinnaql

QA Validation Specialist

Sanford, NC · On-site

Minimum 5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments. * Strong experience supporting equipment qualification from a Quality Assurance perspective.

Pinnaql

QA Validation Specialist

Sanford, NC

Minimum 5 years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments. * Strong experience supporting equipment qualification from a Quality Assurance perspective.

AMRI

Manager, Quality Assurance

Springfield, MO

Manager, Quality Assurance in Springfield, MO Build your future at Curia, where our work has the ... in pharmaceuticals or a related industry Language/Communication Skills Ability to read, analyze ...

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

As of Jun 12, 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.

What does QA do in the pharmaceutical industry?

Quality Assurance (QA) in the pharmaceutical industry ensures that products meet safety, quality, and regulatory standards through activities like audits, documentation review, and process validation. QA professionals develop and implement quality systems, conduct inspections, and ensure compliance with Good Manufacturing Practices (GMP) to prevent defects and ensure product integrity.

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.

Is pharma QA a good career?

Pharmaceutical quality assurance (QA) is a stable and in-demand career that involves ensuring products meet safety and regulatory standards. It typically requires knowledge of Good Manufacturing Practices (GMP), attention to detail, and often certification or training in quality systems. The role offers opportunities for advancement and specialization within the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as a Quality Assurance professional in the pharmaceutical industry, and why are they important?

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.

Which pays more, QA or QC?

In pharmaceutical quality assurance (QA) and quality control (QC) roles, QA positions generally offer higher salaries due to their focus on process improvement, compliance, and oversight, often requiring more experience and certifications. QC roles tend to have slightly lower pay but are essential for testing and inspection tasks. Salary differences can vary based on experience, location, and company size.

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.

What is the role of a quality assurance specialist in pharma?

A quality assurance specialist in pharma is responsible for ensuring that pharmaceutical products meet quality standards and regulatory requirements. They develop and implement quality systems, conduct audits, review documentation, and collaborate with production teams to prevent defects and ensure compliance throughout the manufacturing process.
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Quality Assurance In Pharmaceutical jobs near you

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

synergy

Dallas, TX

Full-time

Medical, Dental, Vision, PTO

Posted 19 days ago

Job description

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. This role involves reviewing procedures, ensuring documentation compliance, conducting internal audits, and assisting with regulatory submissions and inspections.

Key Responsibilities:

  • Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.
  • Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies.
  • Conduct internal audits and inspections to assess compliance with quality systems and regulatory standards.
  • Support preparation and management of regulatory submissions and responses to regulatory agencies.
  • Collaborate with cross-functional teams to ensure compliance throughout product lifecycle.
  • Assist in training laboratory and manufacturing staff on quality system requirements and regulatory standards.
  • Investigate and support resolution of deviations, non-conformances, and CAPA activities.

Education & Experience:

  • Bachelor's degree in life sciences, pharmacy, chemistry, or related field.
  • Minimum 5 years of experience in pharmaceutical GLP/GMP quality assurance and regulatory affairs.
  • Strong knowledge of FDA, EMA regulations, and ICH guidelines.
  • Experience with internal auditing and regulatory inspections.

Requirements

Education:

  • Bachelor's degree in life sciences, pharmacy, chemistry, or a related discipline.

Experience:

  • At least 5 years of hands-on experience in pharmaceutical GLP/GMP QA and regulatory affairs.
  • Familiarity with international regulatory frameworks including FDA, EMA, and ICH guidelines.
  • Proven experience conducting internal audits and supporting regulatory inspections.

Skills:

  • Strong attention to detail and organizational skills.
  • Excellent communication and interpersonal abilities.
  • Ability to work collaboratively with cross-functional teams and manage multiple priorities.
  • Proficiency in quality management systems and documentation practices.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Training & Development

Apply