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Pharmaceutical Inspector Jobs (NOW HIRING)

QA Manufacturing Inspector

Fall River, MA ยท On-site

$17K - $18K/yr

Job Title: QA Manufacturing Inspector - 2nd Shift Job Location: Fall River, MA (On-site) Job Type ... Pharmaceutical Manufacturing Experience Required: 3-15 Years Relocation: Not Available Remote ...

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Company Overview Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility ... visual inspections ยท Enforce good hygiene practices and aseptic techniques in GMP areas ยท ...

Visual Inspector - API 653

Hamilton, OH ยท On-site

$23.50 - $31.25/hr

... Pharmaceuticals.) SIGN-ON BONUS AND RELOCATION ASSISTANCE AVAILABLE FOR QUALIFIED APPLICANTS ... inspection, traditional and advanced NDE/NDT, failure analysis, rope access, materials engineering ...

Join our team as an Inspector I at a leading pharmaceutical manufacturing site in Melrose Park, IL. Why you should apply to be an Inspector I: * Pay Rate: $19.75/hour ($18 base + $1.75 shift ...

Join our team as an Inspector I at a leading pharmaceutical manufacturing site in Melrose Park, IL. Why you should apply to be an Inspector I: * Pay Rate: $19.75/hour ($18 base + $1.75 shift ...

The Quality Assurance (QA) Inspector position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team. The position reports to the Manager of QA and may be ...

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Pharmaceutical Inspector information

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How much do pharmaceutical inspector jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for pharmaceutical inspector in the United States is $27.36, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.49 per hour, depending on experience, location, and employer.

What are some common challenges Pharmaceutical Inspectors face in maintaining compliance during facility inspections?

Pharmaceutical Inspectors often encounter challenges such as staying current with evolving regulations, ensuring consistent documentation practices, and identifying subtle deviations from established protocols. They must balance thoroughness with efficiency during audits, often collaborating with cross-functional teams to clarify procedures and address compliance gaps. Navigating these challenges requires strong attention to detail, excellent communication skills, and a proactive approach to ongoing training and professional development.

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

To thrive as a Pharmaceutical Inspector, you need a solid background in pharmaceutical sciences, quality control, and regulatory compliance, often supported by a relevant degree and experience in the pharmaceutical industry. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and inspection protocols is essential, and certifications such as Certified Quality Auditor (CQA) can be advantageous. Attention to detail, analytical thinking, and effective communication are vital soft skills for accurately assessing processes and reporting findings. These competencies ensure the safety, efficacy, and regulatory adherence of pharmaceutical products, protecting public health and maintaining industry standards.

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

AspectPharmaceutical InspectorQuality Control Analyst
Required CredentialsTypically a degree in pharmacy, chemistry, or related field; certifications like GMP trainingSimilar educational background; often requires GMP or GLP training
Work EnvironmentRegulatory agencies, manufacturing plants, inspection sitesLaboratories, manufacturing facilities, quality testing labs
Employer & Industry UsageRegulatory bodies, pharmaceutical companies, manufacturing plantsPharmaceutical companies, biotech firms, quality assurance labs
Common Search & ComparisonYesYes

Both Pharmaceutical Inspectors and Quality Control Analysts work within the pharmaceutical industry and often share similar educational backgrounds and certifications. However, Pharmaceutical Inspectors primarily focus on regulatory compliance and conducting inspections at manufacturing sites, while Quality Control Analysts perform laboratory testing to ensure product quality. Understanding these differences helps job seekers identify the right career path in pharmaceutical quality assurance and regulatory roles.

What are Pharmaceutical Inspectors?

Pharmaceutical Inspectors are professionals responsible for ensuring that pharmaceutical products are manufactured, stored, and distributed in compliance with regulatory standards and guidelines. They conduct inspections of pharmaceutical facilities, review documentation, and evaluate processes to ensure the quality, safety, and efficacy of medicines. Their work helps protect public health by ensuring that only products meeting legal and safety requirements reach consumers. Inspectors may work for government agencies, such as the FDA or EMA, or within the pharmaceutical industry itself.
More about Pharmaceutical Inspector jobs
What cities are hiring for Pharmaceutical Inspector jobs? Cities with the most Pharmaceutical Inspector job openings:
What are the most commonly searched types of Pharmaceutical Inspector jobs? The most popular types of Pharmaceutical Inspector jobs are:
What states have the most Pharmaceutical Inspector jobs? States with the most job openings for Pharmaceutical Inspector jobs include:
Infographic showing various Pharmaceutical Inspector job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 94% Full Time, 3% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $56,905 per year, or $27.4 per hour.

QA Manufacturing Inspector

Artius Solutions

Fall River, MA โ€ข On-site

$17K - $18K/yr

Full-time

Posted 24 days ago


Job description

Job Title: QA Manufacturing Inspector โ€“ 2nd Shift

Job Location: Fall River, MA (On-site)
Job Type: Full-Time | Non-Exempt
Shift Timing: Second Shift | 03:00 PM โ€“ 11:30 PM (flexible as per business needs)
Industry: Pharmaceutical Manufacturing
Experience Required: 3โ€“15 Years
Relocation: Not Available
Remote Option: Not Available
Travel: Not Required


Job Overview:

We are currently hiring a Quality Assurance Inspector to join our manufacturing quality operations team. This individual will ensure that manufacturing practices and product quality meet required standards during all production phases. The role involves floor-level inspection, testing, and documentation in alignment with cGMP and internal SOPs.


Key Responsibilities:
  • Conduct routine in-process quality checks such as weight, hardness, thickness, disintegration, friability, etc.

  • Perform room and equipment clearance inspections before and after production stages.

  • Execute sampling and inspections based on Acceptable Quality Limits (AQL).

  • Collect product samples for quality testing and ensure proper documentation for lab submissions.

  • Maintain verification logs of balances, weights, and instruments used during inspections.

  • Manage segregation and documentation of rejected batches/materials.

  • Monitor environmental conditions across manufacturing areas.

  • Assist in reviewing equipment calibration, pest control records, temperature logs, and maintenance reports.

  • Review production documentation for completeness and ensure yields/reconciliation accuracy before moving to next steps.

  • Perform complaint sample testing and submit detailed reports.

  • Report deviations, discrepancies, or non-compliance issues to QA leadership.

  • Participate in assigned improvement projects or additional QA activities as needed.


Required Qualifications:
  • Minimum Education: High school diploma required; vocational training or associate degree in pharma or industrial production preferred.

  • Experience: At least 3 years in a GMP-regulated pharmaceutical manufacturing QA role.

  • Dosage Forms: Preferred exposure to inhalation products (MDI); experience with tablets, capsules, liquids, and solids also acceptable.

  • Systems & Tools: Working knowledge of Microsoft Office, ERP (e.g., SAP), and documentation practices.

  • Communication: Must be fluent in spoken and written English.

  • Compliance: Strong understanding of current Good Manufacturing Practices (cGMPs) and standard operating procedures (SOPs).


Desired Skills:
  • High attention to detail with ability to multitask and manage timelines.

  • Strong communication, organizational, and documentation skills.

  • Ability to work independently with minimal supervision on the production floor.

  • Team-oriented mindset and willingness to support cross-functional operations.


Note:
Candidates must have a pure pharmaceutical manufacturing background (not biotech).
Experience with MDI is a strong plus but not mandatory. Candidates with experience in other dosage forms such as solids, liquids, tablets, or capsules will be considered.