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Pharmaceutical Qa Jobs (NOW HIRING)

Sr. Auditor

Paramus, NJ · On-site

$67/hr

Sr. Auditor Quality Assurance (Pharmaceuticals) Location: Paramus, NJ (100% On-Site) - 5 month contract Experience Level: Mid-Senior Experience Required: 5+ Years Education Required: Bachelors Degree ...

The Specialist I helps maintain product quality, compliance, and patient safety by executing defined QA responsibilities and building technical expertise in pharmaceutical quality systems. Reporting ...

The Specialist I helps maintain product quality, compliance, and patient safety by executing defined QA responsibilities and building technical expertise in pharmaceutical quality systems. Reporting ...

Knowledge of FDA 21 CFR Parts 111, 210 and 211 and applicable cGMP pharmaceutical quality requirements * Minimum of 3-5 years of Quality Assurance experience in a GMP-regulated pharmaceutical ...

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Pharmaceutical Qa information

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$10

$46

$73

How much do pharmaceutical qa jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pharmaceutical qa in the United States is $46.70, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $62.02 per hour, depending on experience, location, and employer.

What is a pharmaceutical QA?

Pharmaceutical QA (Quality Assurance) professionals are responsible for ensuring that pharmaceutical products are developed, manufactured, and distributed according to industry standards and regulatory requirements. Their main goal is to maintain product quality and safety by overseeing processes, conducting audits, and implementing quality management systems. They work closely with other departments to ensure compliance with Good Manufacturing Practices (GMP) and other regulations. QA professionals also investigate quality issues, review documentation, and facilitate continuous improvement to prevent future problems.

What are the key skills and qualifications needed to thrive as a pharmaceutical QA, and why are they important?

To thrive as a Pharmaceutical QA, you need a strong background in quality assurance processes, regulatory compliance, and a relevant scientific degree such as pharmacy, chemistry, or biology. Familiarity with Good Manufacturing Practices (GMP), quality management systems (QMS), and industry-standard audit tools or certifications like ISO 9001 is essential. Attention to detail, analytical thinking, and strong communication skills help professionals excel in identifying issues and ensuring adherence to standards. These skills are crucial for maintaining product safety, meeting regulatory requirements, and upholding a company’s reputation in the pharmaceutical industry.

What are some common challenges faced by pharmaceutical QA professionals, and how can they be addressed?

Pharmaceutical QA professionals often encounter challenges such as staying up-to-date with evolving regulatory requirements, managing complex documentation, and ensuring consistent product quality across batches. To address these issues, QA teams typically participate in regular training, implement robust quality management systems, and foster close collaboration with production, R&D, and regulatory affairs departments. Effective communication and proactive problem-solving are also key to maintaining compliance and quickly resolving quality issues as they arise.

What is the difference between Pharmaceutical Qa vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical QaPharmaceutical Quality Control Analyst
CertificationsGMP, GDP, ISO certificationsGMP, GLP, ISO certifications
Work EnvironmentQuality assurance departments, regulatory complianceLaboratories, testing facilities
Primary FocusEnsuring quality processes and complianceTesting and analyzing raw materials and products

Pharmaceutical Qa professionals focus on maintaining quality standards through audits, documentation, and compliance, while Pharmaceutical Quality Control Analysts perform laboratory testing to verify product quality. Both roles are essential in the pharmaceutical industry and often work closely to ensure products meet regulatory requirements.

Is pharmaceutical QA a good career?

Pharmaceutical QA (Quality Assurance) is a stable career that involves ensuring drug manufacturing processes meet regulatory standards and quality requirements. It typically requires attention to detail, knowledge of Good Manufacturing Practices (GMP), and relevant certifications. The role offers opportunities for advancement and is essential in the pharmaceutical industry, which is generally considered a secure sector.
More about Pharmaceutical Qa jobs

What cities are hiring for Pharmaceutical Qa jobs?

Cities with the most Pharmaceutical Qa job openings:

What are the most commonly searched types of Pharmaceutical Qa jobs?

The most popular types of Pharmaceutical Qa jobs are:

What states have the most Pharmaceutical Qa jobs?

States with the most job openings for Pharmaceutical Qa jobs include:

Infographic showing various Pharmaceutical Qa job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $97,144 per year, or $46.7 per hour.

Sr. Auditor

Global Placement Firm

Paramus, NJ • On-site

$67/hr

Contractor

Re-posted 7 days ago


Job description


Sr. Auditor Quality Assurance (Pharmaceuticals)

Location: Paramus, NJ (100% On-Site) - 5 month contract
Experience Level: Mid-Senior
Experience Required: 5+ Years
Education Required: Bachelors Degree (Life Sciences or related field)
Industry: Pharmaceuticals / Life Sciences
Job Function: Quality Assurance / Auditing / Compliance
Compensation: Hourly Competitive (rate provided upon request)
Relocation Assistance: Not Provided
Visa Sponsorship: Not Available


Position Summary

We are seeking a Senior Quality Assurance Auditor with strong experience in the pharmaceutical or radiopharmaceutical sector. This role is responsible for planning, conducting, and reporting on internal and external audits to ensure compliance with GMP, GDP, and other global regulatory standards. The successful candidate will play a critical role in upholding our Pharmaceutical Quality System (PQS) and ensuring inspection readiness across operations.


Key Responsibilities
  • Conduct internal audits, supplier audits, and contract manufacturer (CMO) audits including routine, for-cause, and risk-based.

  • Develop and manage audit plans, schedules, and checklists based on regulatory guidelines and internal SOPs.

  • Assess compliance with FDA, EMA, ICH, and international GMP/GDP regulations.

  • Review and evaluate deviations, CAPAs, and change control records.

  • Generate detailed audit reports and communicate findings to internal and external stakeholders.

  • Track CAPA implementation and verify effectiveness through follow-up assessments.

  • Support regulatory authority inspections and third-party audits.

  • Provide expertise on quality and compliance-related matters, promoting audit readiness culture.

  • Identify systemic gaps, recommend improvements, and drive continuous quality improvement initiatives.

  • Stay current on regulatory changes, industry trends, and quality system best practices.


Required Qualifications

Bachelors degree in Life Sciences, Pharmacy, or a closely related field
5+ years of pharmaceutical QA experience (with at least 2 years conducting audits)
Proven understanding of GMP, GDP, and radiopharmaceutical (RPT) compliance
Familiarity with global regulations including FDA, EMA, ICH
Excellent documentation, communication, and analytical skills
Ability to travel up to 10% for audits (domestic and potentially international)


Preferred Certifications

ASQ Certified Quality Auditor (CQA)
ISO 9001 Lead Auditor Certification
GCP/GMP Auditing Certifications


Why You Should Apply

If you're looking to leverage your audit and compliance skills in a growing, highly specialized sector like radiopharmaceuticals, this role offers the ideal opportunity. You'll work in a critical QA function with visibility across manufacturing, testing, and supply chain operations, helping to uphold product integrity and patient safety.

This is a high-impact position where your attention to detail and regulatory expertise will directly contribute to maintaining compliance, improving systems, and supporting global quality standards. Whether you're looking to step into a senior auditing role or expand your influence across a broader QA landscape, this opportunity provides the structure, challenge, and responsibility to help elevate your career.

Apply now to join a team committed to excellence in pharmaceutical quality and make a difference in the future of healthcare.