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Source Inspection Jobs in Florida (NOW HIRING)

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Source Inspection information

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How much do source inspection jobs pay per hour?

As of May 30, 2026, the average hourly pay for source inspection in Florida is $16.76, according to ZipRecruiter salary data. Most workers in this role earn between $13.46 and $18.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Source Inspector, and why are they important?

To thrive as a Source Inspector, you need strong knowledge of quality assurance principles, inspection procedures, and relevant industry standards, often supported by certifications such as ASQ or ISO auditor credentials. Familiarity with inspection tools, measurement devices, and reporting systems like SAP or QMS software is typically required. Attention to detail, integrity, and effective communication are crucial soft skills for accurately evaluating products and collaborating with suppliers. These skills ensure products meet required specifications, prevent costly defects, and maintain customer trust throughout the supply chain.

What are the typical challenges faced by professionals in Source Inspection roles, and how can they be addressed?

Professionals in Source Inspection often encounter challenges such as balancing strict adherence to quality standards with production deadlines, managing clear communication between suppliers and internal teams, and keeping up with evolving compliance requirements. To address these, it's vital to maintain organized documentation, proactively clarify specifications with all stakeholders, and stay updated on industry standards. Building strong relationships with suppliers and fostering a collaborative approach can also help mitigate misunderstandings and ensure quality outcomes.

What is source inspection?

Source inspection is a quality assurance process where products or materials are inspected at the supplier's facility before they are shipped to the buyer. This helps to ensure that goods meet specified standards, requirements, and contractual agreements, reducing the risk of defects or non-conformities upon delivery. Source inspections are commonly used in industries like manufacturing, construction, and aerospace to maintain high-quality standards and avoid costly rework or delays.

What is the difference between Source Inspection vs Quality Control Inspector?

AspectSource InspectionQuality Control Inspector
CertificationsOften requires certifications like ASQ CQI or specific industry standardsMay require similar certifications, but focus is on inspection procedures
Work EnvironmentConducted at supplier sites or during manufacturing processesPerformed at various stages, including in-house or at production lines
Industry UsageCommon in manufacturing, aerospace, and construction industriesWidely used across manufacturing, automotive, and industrial sectors

Source Inspection focuses on verifying materials and components at the supplier or manufacturing site before delivery, ensuring compliance with specifications. Quality Control Inspectors perform inspections throughout the production process or final product to maintain quality standards. While both roles involve inspection and certifications, Source Inspection emphasizes supplier verification, whereas Quality Control Inspectors focus on ongoing quality assurance during production.

What job categories do people searching Source Inspection jobs in Florida look for? The top searched job categories for Source Inspection jobs in Florida are:
Infographic showing various Source Inspection job openings in Florida as of May 2026, with employment types broken down into 86% Full Time, 8% Part Time, 3% Contract, and 3% Nights. Highlights an 100% In-person job distribution, with an average salary of $34,864 per year, or $16.8 per hour.
Sr. Source Regulatory Compliance Specialist

Sr. Source Regulatory Compliance Specialist

Johnson and Johnson

Palm Beach Gardens, FL • On-site

Full-time

Retirement, PTO

Posted 6 days ago


Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Quality
Job Sub Function:
Quality & Compliance Audit
Job Category:
Professional
All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
DePuy Synthes is recruiting for a Sr. Source Regulatory Compliance Specialist, located in Palm Beach Gardens FL, Raynham MA or West Chester PA. RAYNHAM .
Job Overview
The Sr. Source Regulatory Compliance Specialist is responsible for executing and supporting regulatory compliance activities related to sourcing, suppliers, and externally provided processes. This role ensures that suppliers, contract manufacturers, and sourced materials comply with applicable regulatory requirements, quality system standards, and internal policies. The position plays a key role in safeguarding product quality, supporting audit readiness, and enabling compliant supply continuity by partnering closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams.
Key Responsibilities
  • Execute source regulatory compliance activities to ensure adherence to regulatory and quality system requirements.

  • Support compliance oversight for suppliers, contract manufacturers, and externally provided processes.

  • Partner with Supply Chain, Procurement, Quality, and Regulatory Affairs teams to support compliant supplier qualification and lifecycle management.

  • Interpret regulatory requirements and support translation into sourcing and supplier compliance expectations.

  • Support internal audits, external audits, and health authority inspections related to sourcing and supplier compliance.

  • Monitor compliance risks, trends, and supplier performance metrics; support corrective and preventive actions.

  • Ensure accurate maintenance of compliance documentation, records, and reports.

  • Contribute to continuous improvement initiatives to strengthen sourcing compliance governance and effectiveness.

Qualifications
Education:
  • Bachelor's degree in Regulatory Affairs, Quality, Engineering, Life Sciences, Supply Chain, or a related discipline (required).

  • Advanced degree in a scientific or regulatory field (preferred).

Experience and Skills:
Required:
  • Typically 4-6 years of experience in Regulatory Compliance, Quality, Supply Chain, or related roles within a regulated industry.

  • Working knowledge of regulatory and quality requirements impacting sourcing and supplier operations.

  • Experience supporting supplier audits, inspections, or compliance assessments.

  • Ability to manage complex compliance topics and documentation with strong attention to detail.

Preferred:
  • Experience in medical devices, healthcare, or other highly regulated industries.

  • Familiarity with U.S. regulatory and supplier compliance expectations.

  • Experience working in a global or matrixed organization.

  • Exposure to regulatory inspections involving supplier or contract manufacturing oversight.

  • Quality or Regulatory certifications (e.g., RAC, ASQ).

  • Strong analytical, organizational, and problem-solving skills.

  • Effective written and verbal communication skills.

Other:
  • Language: English required.

  • Travel: Limited; occasional domestic travel.

  • Certifications: Quality or Regulatory certifications preferred but not required.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
#DePuySynthesCareers
Required Skills:
Preferred Skills:
Agile Internal Audit, Analytical Reasoning, Audit and Compliance Trends, Communication, Compliance Management, Compliance Policies, Compliance Risk, Controls Compliance, Critical Thinking, Problem Solving, Quality Auditing, Quality Control (QC), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)
The anticipated base pay range for this position is :
$94,000.00 - $151,800.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
• Vacation -120 hours per calendar year
• Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
• Holiday pay, including Floating Holidays -13 days per calendar year
• Work, Personal and Family Time - up to 40 hours per calendar year
• Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
• Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
• Caregiver Leave - 80 hours in a 52-week rolling period10 days
• Volunteer Leave - 32 hours per calendar year
• Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits