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Pharma Auditor Jobs (NOW HIRING)

TecTammina

Staff/ Senior Financial Auditors

Jersey City, NJ · On-site

$84K - $103K/yr

Look no further.....become part of this top Pharma's Internal Audit Group Leadership Development ... We are looking for several Staff and Senior Auditors, you will be responsible for the completion of ...

West-Rhein-Treuhand Zacharias & Demmer oHG

$70.28 - $93.71/hr

... aktuell Unterstützung durch einen Erfahrenen Prüfer / Prüfungsleiter ... Bereichen Pharma, Metallverarbeitung, Handel, Medizintechnik, Chemische Industrie und ...

Mayne Pharma

Compliance Operations Manager

Raleigh, NC · Hybrid

The Compliance Operations Manager executes the day-to-day operations of Mayne Pharma's Compliance ... Execute compliance monitoring and auditing activities, analyze trends, and communicate findings and ...

Mayne Pharma

Compliance Operations Manager

Raleigh, NC · On-site

The Compliance Operations Manager executes the day-to-day operations of Mayne Pharma's Compliance ... Execute compliance monitoring and auditing activities, analyze trends, and communicate findings and ...

RIS Rx

Be Seen First

Pharmacy Auditor

Irvine, CA · On-site

$21 - $25/hr

Pharmacy Auditor Location: Irvine, CA Reports to: Program Supervisor/Solutions Manager FLSA Status ... pharma manufacturers we serve. We've built the industry's first real-time, pharmacist-led GTN ...

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Pharma Auditor information

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$38.5K

$92.8K

$151K

How much do pharma auditor jobs pay per year?

As of Aug 24, 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?

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What job categories do people searching Pharma Auditor jobs look for?

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Pharma Auditor jobs near you
Infographic showing various Pharma Auditor job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 8% Part Time, 2% Contract, and 1% Nights. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $92,797 per year, or $44.6 per hour.

Quality Auditor III / Pharma External Manufacturing

Pioneer Data

Andover, MA • On-site

Contractor

Re-posted 8 days ago

Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for an Quality Auditor III to join their expanding team.
Job Title: Quality Auditor III / Pharma External Manufacturing
Duration: 15 months contract, extendable up to 48 months
Location: Andover, MA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
External Supply Operations Quality (ESOQ Manager)
 
Role Description:
The Global External Quality Operations Mission is to be a proactive partner, driving a science and risk-based compliant quality culture that is flexible, innovative, and customer oriented, maximizing the contribution of Quality Operations to Our Path Forward initiatives.?
External Supply Operations Quality (ESOQ) is committed to supporting Pfizer Global Supply (PGS) as an innovative and competitive advantage for client by assuring the quality of products manufactured and packaged by other companies (Contractors) for Pfizer.
ESOQ is responsible for the Quality & Regulatory management of approximately 300 contract manufacturers, packagers, and supply partners globally.
 
Responsibilities:
The ESOQ Manager holds overall accountability for assigned CMOs, with primary responsibility for quality oversight (approximately 80%) and secondary responsibility for regulatory oversight (approximately 20%) across operational activities.
The ESOQ Manager is accountable for providing quality assurance management of key contractors for client and for assuring that the products supplied to our patients are manufactured & tested in accordance with c-GMPs, the registration file and any additional country specific requirements.
This is highly independent position operating with minimal supervision, interacting with high levels of management both at contract manufacturers and within client.
(S)he will operate as spokesperson for ESOQ and will focus on developing relationships, independently negotiating, developing and communicating client quality requirements with contract manufacturers.
ESOQ Manager will have significant interactions with many internal business and manufacturing organizations (e.g. External Supply, Regulatory, Technical Support, Quality, PGS sites and R&D) and will lead virtual cross functional teams.
Initiate, review and approve regulatory changes through client enterprise system (i.e. PDM) for changes initiated by or impacting ESOQ managed contractors.
Provide support for the closure of the deficiency letters, CMC Commitments, Regulatory requests for Renewals, New Product Registrations and Post approval variations.
Main point of contact for Global Chemistry, Manufacturing & Controls (CMC) or Local Regulatory Affairs in client Country Offices (Single market prods) for the regulatory activities involving the ESOQ contractors.
As the Quality & Regulatory Expert, participate in Virtual Site Operating Teams (VSOT) for ESOQ managed contractors and if needed, participate in Site Quality visits at the contractors.
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable).
 
Qualifications:
Minimally BA/BS Science, Engineering, or related technical discipline with at least 7 years in a GXP setting and/or Regulatory Affairs role.
At least 4 years of Product Quality Assurance experience in a GMP environment with Aseptic manufacturing experience.
Advanced computer skills, MS Office and enterprise systems such as SAP, QTS, PDM, Documentum platforms.
Command of English language required and multi-lingual is a benefit.
Strong verbal and written communication including presentation skills.
Shows strong negotiation skills and is diplomatic in communication with internal and external customers.
Demonstrated ability to manage multiple projects and priorities.
Demonstrated ability to prioritize work, to act and work independently and to escalate items as required to Team leader.
Demonstrated excellent organization skills.
Demonstrated experience managing complex quality and compliance activities in a manufacturing plant or with a contractor.
Developing personal leadership to manage cross functional projects.
Developing ability to resolve conflicts.
Takes initiatives and is proactive, persistent.
Has a broad GMP and technical know-how to handle emerging issues.
Able to report remotely and deliver work independently.
Up to 20% travel may be required.