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 ...
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 ...
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 ...
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 ...
Director of Quality US
Raleigh, NC · On-site
$130 - $200/hr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Director of Quality US
Raleigh, NC · On-site
$130 - $200/hr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Quick apply
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Quick apply
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
Quick apply
Director of Quality US
Raleigh, NC · On-site
$110K - $130K/yr
Euromed Pharma US Inc is looking for a driven and experienced Director of Quality US to lead and ... FDA, EMA, MHRA) * Auditing experience (internal and external) of suppliers, vendors, and ...
... auditing patient records for accuracy and completion of billing, coding, and clinical documentation. This position answers questions from patients and providers regarding dental insurance benefits ...
... auditing patient records for accuracy and completion of billing, coding, and clinical documentation. This position answers questions from patients and providers regarding dental insurance benefits ...
Insurance Specialist
Chapel Hill, NC · On-site
... auditing patient records for accuracy and completion of billing, coding, and clinical documentation. This position answers questions from patients and providers regarding dental insurance benefits ...
Insurance Specialist
Chapel Hill, NC · On-site
... auditing patient records for accuracy and completion of billing, coding, and clinical documentation. This position answers questions from patients and providers regarding dental insurance benefits ...
Automation Engineer
Zebulon, NC · On-site
Provide subject matter expertise to regulatory inspections and interact with auditors as necessary ... Understanding of FDA PAT initiatives and the impact on the Pharma industry. * Six Sigma and Lean ...
Automation Engineer
Zebulon, NC · On-site
Provide subject matter expertise to regulatory inspections and interact with auditors as necessary ... Understanding of FDA PAT initiatives and the impact on the Pharma industry. * Six Sigma and Lean ...
... Control, auditing, document management, CAPA resolution, etc. * Provide strategic Quality ... Minimum of 10 years in a regulated medical device/pharma manufacturing company, including minimum ...
... Control, auditing, document management, CAPA resolution, etc. * Provide strategic Quality ... Minimum of 10 years in a regulated medical device/pharma manufacturing company, including minimum ...
Automation Engineer
Zebulon, NC · On-site
Provide subject matter expertise to regulatory inspections and interact with auditors as necessary ... Understanding of FDA PAT initiatives and the impact on the Pharma industry. * Six Sigma and Lean ...
Automation Engineer
Zebulon, NC · On-site
Provide subject matter expertise to regulatory inspections and interact with auditors as necessary ... Understanding of FDA PAT initiatives and the impact on the Pharma industry. * Six Sigma and Lean ...
Pharma Auditor information
See Raleigh, NC salary details
$37.4K - $47.4K
3% of jobs
$47.4K - $57.3K
11% of jobs
$57.3K - $67.2K
8% of jobs
$70.5K is the 25th percentile. Wages below this are outliers.
$67.2K - $77.2K
11% of jobs
The median wage is $85.8K / yr.
$77.2K - $87.1K
20% of jobs
$87.1K - $97.1K
13% of jobs
$105K is the 75th percentile. Wages above this are outliers.
$97.1K - $107K
12% of jobs
$107K - $117K
11% of jobs
$117K - $126.9K
9% of jobs
$126.9K - $136.8K
3% of jobs
$136.8K - $146.8K
0% of jobs
$37.4K
$90.2K
$146.8K
How much do pharma auditor jobs pay per year?
How do you become a pharma auditor?
What is a pharmaceutical auditor?
What is the difference between Pharma Auditor vs Quality Control Analyst?
| Aspect | Pharma Auditor | Quality Control Analyst |
|---|---|---|
| Required Credentials | GMP certification, relevant degree (e.g., life sciences) | Laboratory certifications, scientific degrees |
| Work Environment | Auditing facilities, reviewing compliance documents | Laboratories, testing environments |
| Employer & Industry Usage | Pharmaceutical companies, regulatory agencies | Manufacturers, research labs |
| Common Search & Comparison | Yes | No |
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.
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Full-time
Posted 5 days ago
Job description
Position Overview:
The Compliance Operations Manager executes the day-to-day operations of Mayne Pharma's Compliance & Risk Program. Working closely with business stakeholders, this role implements compliance initiatives, manages operational processes, leads cross-functional activities, and supports continuous improvement of the compliance program. The position emphasizes execution, operational excellence, and project management across monitoring, transparency reporting, training, policy administration, and investigations to help ensure compliance with applicable healthcare laws, regulations, and company policies.
The position reports to the VP, Global Head Compliance & Risk and is a hybrid position based in Raleigh, NC.
Specific Responsibilities
Compliance Program Operations
- Develop, implement, and maintain compliance policies, procedures, guidance, and training.
- Manage Compliance Committee meetings, materials, and follow-up activities.
- Deliver compliance onboarding and targeted training for employees, as needed.
- Oversee, in conjunction with Global Head Compliance & Risk, compliance risk assessments and implementation of mitigation activities.
- Lead continuous improvement initiatives that enhance compliance program effectiveness.
- Provide practical compliance guidance to business partners while supporting business objectives.
Monitoring & Transparency
- Execute compliance monitoring and auditing activities, analyze trends, and communicate findings and recommendations.
- Manage operational aspects of federal and state transparency reporting, including data validation, certifications, and disclosures.
- Track remediation activities and support ongoing monitoring of corrective actions.
Investigations
- Own internal investigations, including case intake, evidence collection, interviewing, case tracking, and recommendations for corrective action.
Key Competencies/Requirements:
- Bachelor's degree required.
- Minimum of 5 years of compliance experience in the pharmaceutical, biotechnology, or life sciences industry.
- Knowledge of healthcare compliance laws, regulations, and industry codes (e.g., Anti-Kickback Statute, False Claims Act, FDA promotional requirements, PhRMA Code, etc.).
- Experience supporting compliance monitoring, auditing, policy administration, or operational compliance programs.
- Experience with federal and state transparency reporting, including Open Payments.
- Experience with compliance technologies such as learning management systems, case management systems, expense management systems, or transparency reporting platforms.
- Strong project management and organizational skills with the ability to manage multiple priorities.
- Excellent written and verbal communication skills.
- Strong analytical skills with exceptional attention to detail.
- Ability to build collaborative relationships across business functions and influence without direct authority.
Physical Requirements:
- Occasional travel required
Any communication you receive from Mayne Pharma will never come from a personal email domain or chat service such as "gmail" or "Google Chat". All official communication from Mayne Pharma will be received from our company email domain - @maynepharma.com.