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Vial Inspector Jobs (NOW HIRING)

Senior Manufacturing Engineer

Bridgeton, MO

$86K - $118K/yr

... finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling lines, cappers ... Support regulatory submissions and inspections by preparing technical packages and defending ...

Senior Manufacturing Engineer

Bridgeton, MO

$86K - $118K/yr

... finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling lines, cappers ... Support regulatory submissions and inspections by preparing technical packages and defending ...

Operator I, Non-Aseptic Production

Raleigh, NC · On-site

$16.25 - $19.75/hr

POSITION OVERVIEW The Non-Aseptic Production Operator I position is working in the roles of Vial Inspectors, Component Prep, & Compounding/Formulation. This person would be responsible for the ...

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Vial Inspector information

See salary details

$24.5K

$54.9K

$99K

How much do vial inspector jobs pay per year?

As of Jun 10, 2026, the average yearly pay for 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 are the key skills and qualifications needed to thrive as a Vial Inspector, and why are they important?

To thrive as a Vial Inspector, you need strong attention to detail, manual dexterity, and a high school diploma or equivalent. Familiarity with visual inspection systems, microscopes, and quality control software is often required. Reliability, focus, and the ability to follow strict procedures are crucial soft skills in this role. These skills are vital to ensure product safety, compliance with regulations, and the prevention of defective pharmaceuticals reaching patients.

What are vial inspectors?

Vial inspectors are professionals responsible for examining pharmaceutical vials to ensure they meet quality and safety standards. They check for defects such as cracks, contamination, improper sealing, or particulate matter inside the vials. Vial inspectors often use both visual and automated inspection methods to detect any issues before the products are distributed. Their role is crucial in the pharmaceutical industry to maintain product integrity and patient safety.

What is the difference between Vial Inspector vs Bottle Inspector?

AspectVial InspectorBottle Inspector
Required CertificationsQuality assurance certifications, GMP trainingQuality assurance certifications, GMP training
Work EnvironmentPharmaceutical manufacturing, cleanroomsPharmaceutical or beverage manufacturing, cleanrooms
Industry UsagePharmaceuticals, biotechPharmaceuticals, beverages, cosmetics
Common Search/ComparisonYesYes

Vial Inspectors and Bottle Inspectors both work in manufacturing environments requiring GMP compliance and quality assurance certifications. Vial Inspectors focus on inspecting small glass containers used in pharmaceuticals, while Bottle Inspectors typically handle larger bottles in beverage or cosmetic industries. Both roles involve ensuring product safety and quality, but they differ mainly in the type of containers inspected and industry specifics.

What are some common challenges faced by Vial Inspectors and how can they be managed?

Vial Inspectors often face challenges such as maintaining high levels of concentration during repetitive tasks and ensuring accuracy while inspecting large volumes of vials. Managing these challenges involves taking regular breaks, adhering strictly to safety and quality protocols, and using available automated systems to reduce manual strain. Collaborating closely with quality assurance teams and participating in ongoing training can also help inspectors stay up-to-date with best practices and industry standards.
More about Vial Inspector jobs
What are the most commonly searched types of Vial Inspector jobs? The most popular types of Vial Inspector jobs are:
Infographic showing various Vial Inspector job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $54,939 per year, or $26.4 per hour.
Director, Formulation and Process Development

Director, Formulation and Process Development

AstraZeneca

New Haven, CT • On-site

$175K - $263K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago


AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical


Job description

You will lead and direct the formulation and process development of patient-centered injectable drug products.These products are for Alexion's diverse portfolio, which spans synthetic, peptide, genomic medicine, and protein-based modalities in multiple formats, including liquid, lyophilized, vial, prefilled, and cartridge-based presentations. You will also lead life cycle development opportunities, provideexpertisein technology transfer and drug product engineering and technology development with internal and external partnerships. You will also ensure the development of portfolio projects in a phase-appropriate manner while managing the budget and interface partners. You will be a member of the Injectable Drug Product Management team and will need to collaborate and network with other departments within Product Development and Clinical Supplies (PDCS). Additionally, it will need to collaborate and network with Alexion Operations, Clinical Development, Quality, and Regulatory organizations.

You Will:

  • Formulation and process development and manufacturing of patient-centered, unique injectable drug products for Alexion's diverse portfolio from pre-clinical to successful licensure.

  • Develop drug productdevelopmentstrategies through internal/external partnerships and product integration into drug/device combination products.

  • Enablethe progression of Alexion'sdiverse portfoliothatspans peptide, nucleic acid, protein-based modalities, as well as modalities for gene deliveryasliquid and lyophilized dosage forms in vial, prefilled syringe, and cartridge-based presentations.

  • Ensure tech transfer of Alexion's portfolio with specialized input on engineering solutions for equipment and processes.

  • Review and develop drug producttechnologyroadmap and manage important investments.

  • Mentorand developcolleagues in a matrix team for efficient and successful drug product development and manufacturing in a phaseappropriate manner.

  • Partner with functions across Alexion to build the best strategies for developing products in Alexion's diverse portfolio.

  • Provide subject matterexpertisefor preparing regulatory filings, regulatory interactions including inspections, audits and is accountable for the technical content of the relevant drug product sections of regulatory submissions.

  • Work with the Head on the developmentondrug product development strategies within PDCS and with partners in Operations, Regulatory Affairs, and Commercial organizations.

You Have:

  • Must have a BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related discipline with relevant experience

  • At least 8 years of experience in managing a group of drug product development scientists or engineers withendtoenddrug product developmentexperience(spanning formulation, process development, quality attribute assessment,techtransferand manufacturing support)formAbs,fusionproteins,injectablepeptides/syntheticsprograms.

  • At least 5 years of experience managing a team of scientists and engineers atdifferent levels(directly or in a matrix team)and ensuring their career growth.

  • Must be proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment,regulatory expectationsand applying these to developing efficient approaches to ensure product licensure.

  • Knowledge of high concentration protein formulation development, aseptic processes, vial, prefilled syringe, cartridge presentations,liquid and lyophilization dosage forms is important.

  • Knowledge of current regulatory guidelines and cGMP requirements is necessary

Benefits offered include:

  • A qualified retirement program [401(k) plan]

  • Paid vacation, holidays, and paid leaves

  • Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans.

Additionaldetails of participation in these benefit plans will be provided if an employee receives an offer of employment.The annual base salary for this position ranges from $175,000 to $263,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility toparticipatein our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).

#LI-Onsite #Alexion

Date Posted

29-May-2026

Closing Date

29-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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