ZipRecruiter

Log In

1

Hourly Vial Inspector Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsTransportation And Storage JobsWarehousing JobsWarehouse Packer JobsHourly Vial Inspector Jobs

Hourly Vial Inspector information

See salary details

$24.5K

$54.9K

$99K

How much do hourly vial inspector jobs pay per year?

As of Sep 13, 2026, the average yearly pay for hourly vial inspector in the United States is $54,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,500.00 and $63,500.00 per year, depending on experience, location, and employer.

What is the difference between Hourly Vial Inspector vs Quality Control Technician?

AspectHourly Vial InspectorQuality Control Technician
CertificationsMay require GMP or FDA trainingOften requires GMP, FDA, or industry-specific certifications
Work EnvironmentPharmaceutical or biotech manufacturing facilitiesManufacturing, laboratory, or production settings
Job FocusInspecting vials for defects, contamination, and labeling accuracyEnsuring product quality, compliance, and process improvements

Hourly Vial Inspectors primarily focus on visual inspection of vials in pharmaceutical manufacturing, ensuring product quality at the production line. Quality Control Technicians have a broader role, including testing, documentation, and process validation. While both roles require attention to detail and GMP knowledge, QC Technicians often hold additional certifications and perform more comprehensive quality assessments.

What are the most commonly searched types of Vial Inspector jobs?

The most popular types of Vial Inspector jobs are:

What states have the most Hourly Vial Inspector jobs?

States with the most job openings for Hourly Vial Inspector jobs include:

What are popular job titles related to Hourly Vial Inspector jobs?

For Hourly Vial Inspector jobs, the most frequently searched job titles are:

Hourly Vial Inspector jobs near you
Infographic showing various Hourly Vial Inspector job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 55% Full Time, 38% Part Time, 1% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $54,939 per year, or $26.4 per hour.

Quality Assurance Auditor I - 1st Shift

Syracuse, NY • On-site

Steri--pharma-LLC
See more jobs at Steri--pharma-LLCexternal

$24 - $30/hr

Other

Posted 12 days ago

Key responsibilities

  • Perform line checks including in process testing, component verification, bar code operation, sample review, aseptic monitoring and end item inspection.

  • Complete line clearance inspections, including reviews of area logs for proper documentation prior to lot processing, and check in all components prior to use for production.

  • Review and approve production records along with associated production paperwork prior to issuance, ensuring all calculations are correct.

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Assurance Auditor I - 1st Shift

Full Time Technical Syracuse, NY, US

6 days ago Requisition ID: 2614

Salary Range: $24.00 To $30.00 Hourly

Quality Assurance Auditor - 1st Shift 9am-7:30pmHow this position makes a difference:

This position performs critical inspection duties such as line coverage, audit reviews, and monitoring charts. Position is required to complete all required paperwork and data entry specific to quality assurance monitoring.

Duties & Responsibilities:
  • Perform line checks including in process testing, component verification, bar code operation, sample review, aseptic monitoring and end item inspection.
  • Complete line clearance inspections, including reviews of area logs for proper documentation prior to lot processing. Check in all components prior to use for production.
  • Review and approve production records along with associated production paperwork prior to issuance. Ensure all calculations are correct.
  • Perform batch record reviews for accuracy and compliance to company procedure.
  • Oversee the documentation of production interventions as needed.
  • Area purges (packaging and/or vial wash).
  • Shelf reserve sampling, reviews, TRRs and documentation.
  • Successfully complete Manual Inspection Qualification for vial inspections.
  • Attends meetings as required or requested.
  • Promote a safe and harmonious work environment.
  • Maintain compliance with SOPs, GMPs, and all company policies.
  • Other duties as assigned or required.
Requirements:
  • Associates degree from a regionally accredited institution in science or related field.
  • Minimum 1 year quality assurance experience in pharmaceutical or other highly regulated industry.
  • Knowledge of general computer functions such as Microsoft Office programs, spreadsheets, etc.
  • Knowledge in quality auditing practices.
  • Knowledge and understanding of processes relevant to quality compliance of the manufacturing and production of regulated products, regulatory and development processes, regulatory cGMP requirements for pharmaceuticals, regulatory entity inspections requirements, regulatory guidance documents.
  • Knowledge of HACCP and other audit schemes.
  • Skill in handling several projects or tasks at the same time, or within a given time frame.
  • Advanced Problem Safety Sensitivity; the ability to recognize a safety issue or potential safety issue.
  • Skill to use time management techniques in personal daily tasks and that of others.
  • Skill in quality and compliance vigilance.
  • Ability to inspect the work of others and coach performance in line with company standard operating procedures.
  • Ability to apply critical thinking.
  • Advanced interpersonal and communication skills.
  • Ability to effectively articulate and present the company’s quality strategy to our employees, senior management, regulatory bodies and customers.
  • Ability to be flexible in work hours.
  • Ability to provide motivational support.
  • Ability to maintain a professional, positive attitude at all times.
  • Advanced project management and documentation skills.
  • Ability to use training/instructional methods and procedures appropriate for the situation and audience.
  • Ability to instruct/teach one on one on how to perform functions.
  • Ability to trust, develop, maintain, and strengthen partnerships with others inside the organization who can provide information, assistance, and support.
  • Ability to work with minimal supervision and lead by example.
  • Ability to communicate with coworkers, management team members, and other individuals in a courteous and professional manner.
  • Ability to work in a fast-paced environment.
  • Ability to detail and coordinate various activities simultaneously.
#J-18808-Ljbffr

Apply