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Senior Specialist Api Inspector Jobs in Riverside, CA

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA · On-site

$84K - $120K/yr

We are seeking an experienced Sr. Regulatory Affairs Specialist to support global regulatory ... Conducts audits and inspections of GMP and non-regulated documentation. * Tracks internal and ...

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA · On-site

$84K - $120K/yr

Description Position at Prismatik We are seeking an experienced Sr. Regulatory Affairs Specialist ... Conducts audits and inspections of GMP and non-regulated documentation. * Tracks internal and ...

Karman Space & Defense

Senior EHS Specialist

Corona, CA · On-site

$90 - $120/hr

Senior EHS Specialist Full Time Professional Corona, CA, US 16 days ago Requisition ID: 3807 Salary ... Standardizes inspection programs focused on identifying and eliminating safety, health, and ...

Esri

Sr. Generative AI Software Developer

Redlands, CA

$54.75 - $72.50/hr

... specialists to create robust, production-ready software that transforms and advances geospatial ... Strong understanding of object-oriented principles, software architecture, and API design * Ability ...

Esri

Sr. Software Development Engineer - Gen AI

Redlands, CA

$123K - $162K/yr

... specialists to create robust, production-ready software that transforms and advances geospatial ... Strong understanding of object-oriented principles, software architecture, and API design * Ability ...

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Showing results 21-40

All JobsSpecialist Api Inspector JobsSenior Specialist Api Inspector JobsSenior Specialist Api Inspector Jobs in Riverside, CA

Senior Specialist Api Inspector information

See Riverside, CA salary details

$45.9K

$102.3K

$141.4K

How much do senior specialist api inspector jobs pay per year?

As of Sep 3, 2026, the average yearly pay for senior specialist api inspector in Riverside, CA is $102,332.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,100.00 and $118,400.00 per year, depending on experience, location, and employer.

What is the difference between Senior Specialist Api Inspector vs Api Inspector?

AspectSenior Specialist Api InspectorApi Inspector
CertificationsAPI certifications, possibly advanced or specializedAPI certifications, entry to mid-level
Work EnvironmentInspection of pipelines, refineries, industrial facilitiesInspection of pipelines, industrial plants, field sites
Employer & IndustryOil & gas, energy, industrial sectorsOil & gas, energy, industrial sectors
Job ResponsibilitiesSupervising inspections, reviewing compliance, mentoringPerforming inspections, documenting findings, ensuring safety

The main difference is that a Senior Specialist Api Inspector typically has more experience, advanced certifications, and supervisory responsibilities compared to an Api Inspector. Both roles work in similar environments within the oil and gas industry, but the senior role involves leadership and oversight functions.

What are popular job titles related to Senior Specialist Api Inspector jobs in Riverside, CA?

For Senior Specialist Api Inspector jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Senior Specialist Api Inspector jobs in Riverside, CA look for?

The top searched job categories for Senior Specialist Api Inspector jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Senior Specialist Api Inspector jobs?

Cities near Riverside, CA with the most Senior Specialist Api Inspector job openings:

Senior Specialist Api Inspector jobs near you
Infographic showing various Senior Specialist Api Inspector job openings in Riverside, CA as of July 2026, with employment types broken down into 91% Full Time, 3% Part Time, and 6% Contract. Highlights an 76% Physical, 5% Hybrid, and 19% Remote job distribution, with an average salary of $102,332 per year, or $49.2 per hour.

Regulatory Affairs Specialist, Sr.

Prismatik

Irvine, CA • On-site

$84K - $120K/yr

Full-time

Re-posted 22 days ago

Job description

We are seeking an experienced Sr. Regulatory Affairs Specialist to support global regulatory compliance and drive highimpact submissions. In this role, you'll lead FDA 510(k)/PMA filings, maintain international registrations, support audits, develop SOPs, and partner closely with technical teams to ensure products meet regulatory and quality standards. If you excel at interpreting regulations, managing complex documentation, and guiding teams through compliance requirements, this is an opportunity to make a meaningful impact in a fastmoving, innovative environment.
Essential Functions:
  • Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.
  • Maintains company registrations and device listings in the US, Canada, and the EU.
  • Analyzes and reports department metrics.
  • Supports and maintains technical files, MDD certifications, and declarations of conformity in support of EU product registrations/CE mark.
  • Informs coordinator of product recalls.
  • Performs and supports internal, external, and third-party audits.
  • Maintains knowledge on current regulations and guidelines.
  • Evaluates compliance with applicable regulations, project policies, and procedures
  • Reviews and writes standard operating procedures (SOPs) and other RA/QA policies as necessary.
  • Collaborates with technical staff to foster understanding of SOPs and guidance documentation.
  • Composes audit plans and reports.
  • Conducts audits and inspections of GMP and non-regulated documentation.
  • Tracks internal and external corrective and preventive actions.
  • Performs other related duties and projects as business needs require at direction of management.
Knowledge and Abilities:
  • Proficient knowledge of general office procedures.
  • Proficient skills in the MS Office Suite (Excel, Word, PowerPoint, and Outlook).
  • Proficient quantitative and analytical skills.
  • Demonstrated prioritization and time management skills.
  • Demonstrated negotiation abilities.
  • Demonstrated knowledge and understanding of related State and Federal regulations and procedures.
  • Demonstrated high standard of quality of work.
  • Demonstrated knowledge of FDA 510K and ISO 13485 Standards.
  • Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections).
  • Demonstrated reliability, dependability, and flexibility in work habits.
  • Demonstrated attention to detail and accuracy.
  • Ability to analyze and collate data for presentations and reports.
  • Ability to prioritize and organize project tasks and goals effectively.
  • Ability to maintain confidentiality, exhibiting high level of integrity, and trustworthiness.
  • Ability to interpret and collate data to present an accurate picture of market potential.
  • Ability to research new and emerging technologies and practices.
  • Ability to read technical diagrams, graphs, and instructions.
Education and Experience:
  • Bachelor's degree in related field preferred
  • Minimum five (5) years of experience in Regulatory Affairs.
Pay Range: $84,716.01 - $120,000.00/YR
Employment Type: full-time

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