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3Rd Shift Quality Inspector Jobs in Philadelphia, PA

... third party or audit requirements * Communicates effectively with customer, cuppliers and other ... quality systems and processes * Supports and Participates in inspection, audits, may lead some ...

... third party or audit requirements * Communicates effectively with customer, cuppliers and other ... quality systems and processes * Supports and Participates in inspection, audits, may lead some ...

The Opportunity Quality Inspector Inspects product using established specifications that ensure ... Shift 1st/2nd/3rd 1st shift-6a.m.-2p.m. 2nd shift-2p.m.-10p.m. 3rd shift 10p.m.-6a.m. What You'll ...

Quality Inspector

North Wales, PA · On-site

$20 - $22/hr

... work shift (excluding lunch and breaks): stand, walk, sit, squat or bend, kneel and rise, lift ... Any assessment will be performed by a third party vendor and will be reported on a pass/fail basis ...

Coordinate with suppliers and third-party providers to sort, rework, or otherwise disposition ... Enter and maintain inspection, calibration, and quality data in spreadsheets and databases.

Inspector We are seeking three experienced Inspectors for the first shift who will be responsible for conducting quality assessments and measurements on products within specified dimensions.

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3Rd Shift Quality Inspector information

See Philadelphia, PA salary details

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How much do 3rd shift quality inspector jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for 3rd shift quality inspector in Philadelphia, PA is $20.58, according to ZipRecruiter salary data. Most workers in this role earn between $16.25 and $23.27 per hour, depending on experience, location, and employer.

What does a 3rd shift quality inspector do?

A 3rd Shift Quality Inspector is responsible for monitoring and inspecting products during overnight hours to ensure they meet quality standards and specifications. Their duties typically include examining materials, conducting tests, documenting results, and reporting any defects or issues to supervisors. They play a crucial role in maintaining product consistency and safety, especially in manufacturing environments that operate around the clock. Working the '3rd shift' usually means working late-night to early-morning hours.

What are the key skills and qualifications needed to thrive as a 3rd shift quality inspector?

To thrive as a 3rd Shift Quality Inspector, you generally need a high school diploma or equivalent, strong attention to detail, and experience with quality control processes. Familiarity with inspection tools like calipers, micrometers, and quality management systems (QMS) software is often required. Strong communication, problem-solving skills, and the ability to work independently during overnight hours help individuals excel in this role. These skills ensure product standards are maintained and production issues are addressed promptly, supporting overall manufacturing quality and efficiency.

What are some unique challenges faced by 3rd shift quality inspectors, and how can they be managed?

3rd Shift Quality Inspectors often encounter challenges such as working with reduced onsite support and adapting to overnight hours, which can impact communication and alertness. To manage these, inspectors typically rely on detailed shift handover notes, strong self-motivation, and proactive communication with both day and night teams. Maintaining a consistent sleep schedule and utilizing available resources for troubleshooting helps ensure quality standards are met across all shifts. Being adaptable and collaborative is key to success in this role.

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For 3Rd Shift Quality Inspector jobs in Philadelphia, PA, the most frequently searched job titles are:

What job categories do people searching 3Rd Shift Quality Inspector jobs in Philadelphia, PA look for?

The top searched job categories for 3Rd Shift Quality Inspector jobs in Philadelphia, PA are:

What cities near Philadelphia, PA are hiring for 3Rd Shift Quality Inspector jobs?

Cities near Philadelphia, PA with the most 3Rd Shift Quality Inspector job openings:

Infographic showing various 3Rd Shift Quality Inspector job openings in Philadelphia, PA as of August 2026, with employment types broken down into 81% Full Time, 9% Part Time, 2% Contract, and 8% Nights. Highlights an 98% In-person, and 2% Remote job distribution, with an average salary of $42,803 per year, or $20.6 per hour.

Quality Inspector - 3rd shift

Piramal Pharma Limited

Sellersville, PA • On-site

Full-time

Posted 29 days ago


Job description

Be the First to Apply

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Quality Inspector - 3rd shift

Job Description

The Quality Operations Inspector is responsible for providing on-the-floor quality oversight and support to ensure the compliance of manufacturing, packaging, labeling, and distribution operations with Piramal Standard Operating Procedures (SOPs) and applicable regulatory requirements. This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining product quality, safety, efficacy, and regulatory compliance across operations. This is a third shift position working from 10pm - 7am.

Key Responsibilities

  • Issue batch records in alignment with the production schedule to support timely manufacturing activities and Perform potency calculations as applicable.
  • Conduct line clearance and batch readiness assessments, including verification of concurrent documentation, equipment status, and preventive maintenance records.
  • Review and evaluate Environmental Monitoring (EM) data for compliance with internal standards and regulatory requirements.
  • Perform BMS alarms review, acknowledgement and evaluate quality impact. Escalate critical alarms to Management.
  • Perform quality oversight for water system releases used in operations.
  • Perform raw material Sampling and AQL inspection of finished products.
  • Review equipment logbooks and executed batch records to ensure adherence to GDP, GMP, and Data Integrity standards.
  • Scan reviewed batch records and upload to share point.
  • Prepare batch records and perform first release of batches.
  • Perform Raw material reconciliation and investigation.
  • Review and approve Calibration activities in ProCal.
  • Perform QA review and approval of non-routine workorders in SAP.
  • Draft, revise, and review Quality Assurance SOPs and deviation reports to ensure clarity, accuracy, and regulatory alignment.
  • Conduct weekly quality surveillance activities, including facility inspections, environmental monitoring checks, and audits of equipment maintenance and GMP practices to support continuous audit readiness.
  • Complete all assigned training on SOPs and job-related tasks in a timely manner.
  • Stay current with industry trends, updates to regulatory requirements, and emerging quality standards.
  • Perform all other activities as assigned by Manager
Qualifications
  • Bachelor of Science
  • minimum 3 years of experience in pharmaceutical quality assurance, regulatory affairs, or GMP auditing.
  • minimum 3 years Prior experience in providing on-the-floor quality oversight and conducting inspections or working in a regulated pharmaceutical environment preferred.
Skills
  • In-depth knowledge of GMP, GDP, GLP, and relevant international regulations (FDA, EMA).
  • Strong analytical, attention to detail investigative, and problem-solving skills.
  • Excellent communication (written and verbal) and interpersonal skills.
  • Proficiency in MS Office and quality management systems (QMS).
  • Ability to travel to facilities for inspections (as required).