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$38.5K

$92.8K

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How much do pharma auditor jobs pay per year?

As of Jun 4, 2026, the average yearly pay for pharma auditor in the United States is $92,797.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $112,000.00 per year, depending on experience, location, and employer.

What is the difference between Pharma Auditor vs Quality Control Analyst?

AspectPharma AuditorQuality Control Analyst
Required CredentialsGMP certification, relevant degree (e.g., life sciences)Laboratory certifications, scientific degrees
Work EnvironmentAuditing facilities, reviewing compliance documentsLaboratories, testing environments
Employer & Industry UsagePharmaceutical companies, regulatory agenciesManufacturers, research labs
Common Search & ComparisonYesNo

Pharma Auditors focus on evaluating compliance with regulations and standards through audits, while Quality Control Analysts perform laboratory testing to ensure product quality. Both roles require scientific credentials but differ in daily tasks and work environments.

More about Pharma Auditor jobs
What cities are hiring for Pharma Auditor jobs? Cities with the most Pharma Auditor job openings:
What states have the most Pharma Auditor jobs? States with the most job openings for Pharma Auditor jobs include:
What job categories do people searching Pharma Auditor jobs look for? The top searched job categories for Pharma Auditor jobs are:
Pharma Auditor jobs near you
Infographic showing various Pharma Auditor job openings in the United States as of May 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $92,797 per year, or $44.6 per hour.
Quality Control Auditor

Quality Control Auditor

Catalent Pharma Solutions

Winchester, KY • On-site

Full-time

Life, Retirement, PTO

Posted 2 days ago

Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 71 rated pharmaceutical

Job description

Quality Control Auditor

Position Summary

  • Typical working hours for the position are Monday-Friday 8 AM-5 PM.

  • This position is 100% on-site in Winchester, Kentucky.

Catalent's Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology.

The Quality Control Auditor supports release of all materials from the quality control lab. The Quality Control Auditor is responsible for GMP and technical review of raw materials/in process/finished goods data for release.

The Role

  • Support release of raw materials, in-process, finished product by reviewing GMP documents (data, notebooks, certificate of analysis, validation/qualification reports, etc) for compliance to internal SOPs and approved test methods as well as technical accuracy

  • Read and understand test methods from multiple compendia (i.e. USP/NF, EP, JP), internal Catalent methods, or customer/supplier methods+

  • Participate in customer/agency audits as necessary

  • Assist in training QC Analysts

  • Perform analytical testing as needed

  • Assist in laboratory investigations

  • Draft or review standard operating procedures as needed

  • Draft or review CAPAs and audit responses as needed

  • Other duties as required in support of Catalent Pharma Solutions high performance

The Candidate

  • Bachelor's degree in a scientific field (Chemistry or Biology preferred) with 3+ years in a Quality, Laboratory, Clinical, or Chemical Manufacturing Role (including internships or co-op experience).

  • Ability to work well under pressure and maintain efficiency both on an individual and team basis.

  • General computer literacy including use of Microsoft Word and Excel.

  • Previous analytical testing experience is preferred. Experience in the pharmaceutical industry preferred.

  • Proven ability to support multiple project initiatives or multiple projects (either in-process, finished products or raw materials) simultaneously while meeting customer deadlines and producing high quality work and documentation with minimal training, supervision and direction. Proven track record of success of obtaining high quality results with minimal error problem reports and a minimal amount of write-up corrections

  • Individual may be required to sit and stand for an extended period of time. Specific vision requirements include reading of written documents and frequent use of computer monitor and chemical testing materials.

Why You Should Join Catalent

  • Several Employee Resource Groups focusing on D&I

  • Tuition Reimbursement- Let us help you finish your degree or earn a new one!

  • Generous 401K match

  • 152 hours accrued PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media

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