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International Api Inspector Jobs in Anderson, SC

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International Api Inspector information

See Anderson, SC salary details

$22.4K

$50.3K

$90.6K

How much do international api inspector jobs pay per year?

As of Sep 7, 2026, the average yearly pay for international api inspector in Anderson, SC is $50,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,200.00 and $58,100.00 per year, depending on experience, location, and employer.

What is an International API Inspector?

International API Inspectors are professionals who assess and verify that equipment and processes in industries such as oil, gas, and petrochemicals comply with standards set by the American Petroleum Institute (API). Their work involves inspecting pipelines, storage tanks, pressure vessels, and other infrastructure to ensure safety, reliability, and regulatory compliance. They may travel globally to perform inspections, audits, and certifications, ensuring that operations meet both local and international industry standards.

What are some of the unique challenges faced by an International API Inspector when working across different countries?

International API Inspectors often encounter challenges such as adapting to varying safety standards, regulations, and workplace cultures in different countries. They must be flexible and knowledgeable about both local and international API codes to ensure compliance in each location. Communication barriers and coordinating with diverse teams can also require strong interpersonal skills. Additionally, frequent travel and adjusting to new environments can be demanding, but these experiences also offer valuable professional growth and cross-cultural expertise.

What are the key skills and qualifications needed to thrive as an International API Inspector, and why are they important?

To excel as an International API Inspector, you need in-depth knowledge of API standards, inspection procedures, and a relevant technical background—often with certifications like API 510, 570, or 653. Familiarity with inspection tools, non-destructive testing (NDT) methods, and reporting software is typically required. Attention to detail, strong analytical thinking, and effective communication skills help inspectors identify issues and clearly document findings across diverse teams. These abilities are crucial for ensuring compliance, maintaining safety, and upholding industry standards in global inspection environments.

What is the difference between International Api Inspector vs API Inspector?

AspectInternational Api InspectorAPI Inspector
CertificationsAPI certifications, international safety standardsAPI certifications, local safety standards
Work EnvironmentGlobal projects, international companiesDomestic projects, local companies
Industry UsageOil & gas, petrochemical industries worldwideOil & gas, petrochemical industries locally

The International Api Inspector typically works on global projects requiring international certifications and standards, while the API Inspector focuses on domestic safety standards within local industries. Both roles involve inspection and safety compliance but differ mainly in scope and geographic focus.

What are popular job titles related to International Api Inspector jobs in Anderson, SC?

For International Api Inspector jobs in Anderson, SC, the most frequently searched job titles are:

What job categories do people searching International Api Inspector jobs in Anderson, SC look for?

The top searched job categories for International Api Inspector jobs in Anderson, SC are:

What cities near Anderson, SC are hiring for International Api Inspector jobs?

Cities near Anderson, SC with the most International Api Inspector job openings:

International Api Inspector jobs near you
Infographic showing various International Api Inspector job openings in Anderson, SC as of August 2026, with employment types broken down into 80% Full Time, 18% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $50,290 per year, or $24.2 per hour.

Director, Quality Compliance (DEA)

Kelly Services

Greenville, SC

$180K - $220K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago

Key responsibilities

  • Develop and implement enterprise quality compliance strategies, programs, and policies.

  • Lead inspection readiness programs and provide on-site support during regulatory inspections.

  • Manage internal and external audit programs, review audit observations, and drive CAPA implementation.

Job description

Sr. Director of Quality Compliance (DEA)

Full-Time | Senior Leadership

Location: Greenville, SC (Onsite Role)

Compensation: Approximately $180,000-$220,000 base salary + bonus potential

Position Summary

A growing pharmaceutical manufacturing organization is seeking a Sr. Director of Quality Compliance to lead enterprise-wide compliance strategy, governance, audit readiness, inspection management, escalation processes, and quality risk management activities. This individual will serve as a key member of the Quality Leadership team and will drive continuous improvement initiatives to ensure sustained compliance with cGMP, FDA, DEA, DSCSA, and international regulatory requirements.

This role will oversee quality compliance systems and inspection readiness programs while partnering cross-functionally with Quality, Manufacturing, Regulatory, Supply Chain, and Executive Leadership teams. The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory inspections, auditing, and enterprise compliance strategy within GMP-regulated manufacturing environments.

Key Responsibilities

Quality Compliance & Regulatory Oversight

  • Develop and implement enterprise quality compliance strategies, programs, and policies
  • Ensure compliance with FDA, DEA, cGMP, ICH, DSCSA, and global regulatory requirements
  • Lead inspection readiness programs and provide on-site support during regulatory inspections
  • Serve as the primary escalation point for significant quality and compliance risks
  • Manage quality notification-to-management and escalation programs
  • Interpret evolving regulatory requirements and implement systemic compliance improvements

Audit & Inspection Management

  • Direct internal audit programs across manufacturing and quality operations
  • Lead and manage external audits conducted by FDA, DEA, notified bodies, clients, and global health authorities
  • Review audit observations and drive effective CAPA implementation
  • Maintain audit-ready quality systems and documentation practices
  • Track and trend quality indicators and compliance metrics

Quality Systems & Risk Management

  • Oversee core Quality Management System (QMS) processes including:
  • Change control
  • Deviations
  • CAPAs
  • Document management
  • Supplier quality
  • Escalation management
  • Analyze quality data and trends to identify systemic risks and improvement opportunities
  • Ensure effective statistical monitoring and reporting of quality compliance metrics
  • Support post-market surveillance and ongoing product quality monitoring activities

Leadership & Cross-Functional Collaboration

  • Lead and develop Quality Compliance teams and associated quality personnel
  • Partner with Manufacturing, Quality Control, Regulatory Affairs, and Executive Leadership to drive strategic quality initiatives
  • Foster a culture of compliance, accountability, and continuous improvement
  • Support implementation of quality-focused operational efficiencies and business improvements
  • Present quality compliance updates and risk assessments to senior leadership

Continuous Improvement & Strategy

  • Drive initiatives focused on improving inspection outcomes, audit performance, and overall quality culture
  • Lead implementation of systemic process improvements across manufacturing and quality operations
  • Evaluate and enhance quality systems effectiveness through analytics and risk management principles
  • Support modernization initiatives involving predictive analytics, technology platforms, and quality data visibility

Qualifications

Required Education & Experience

  • Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or related scientific discipline
  • 15+ years of progressive pharmaceutical quality experience within GMP-regulated manufacturing environments
  • Prior senior leadership experience in Quality Compliance, Quality Assurance, or Regulatory Compliance
  • Strong experience interacting directly with FDA and global regulatory agencies

Technical Expertise

  • Deep knowledge of:
  • cGMP regulations
  • FDA and global regulatory requirements
  • DEA compliance
  • Quality systems and auditing
  • Risk management principles
  • Pharmaceutical manufacturing operations
  • Experience supporting API, aseptic, sterile, or OTC manufacturing environments preferred
  • Strong understanding of:
  • Deviations
  • CAPAs
  • Change controls
  • Inspection readiness
  • Supplier quality management
  • Data integrity

Additional Information

  • Travel up to approximately 40% may be required
  • Relocation assistance may be available
  • Experience within pharmaceutical manufacturing, CDMO, or highly regulated GMP environments strongly preferred

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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