Regulatory Jobs
Hero Gradient Background
Crowds of Johnson & Johnson employees outside the company's world headquarters in New Brunswick
Johnson & Johnson logo

New · posted Oct 27

Johnson & Johnson · Pharmaceuticals

QC Incoming Inspector

  • Gurabo, PR
  • On-site
  • Full-time
  • Associate & Specialist
Save
EmploymentFull-time
DeadlineCloses Nov 2, 2026

The role

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.

You will be responsible for

  • Performs sampling, inspection, testing, and approval of packaging components in accordance with internal and external regulations and policies, ensuring compliance with supply chain approval cycle time goals.
  • Performs sampling and testing of raw materials in accordance with internal and external regulations and policies, ensuring compliance with supply chain cycle time goals.
  • Inspects labeling, quantity, and materials or products to be shipped.
  • Maintains the Retention Room in an organized manner.
  • Audits the Certificate of Analysis and Certificate of Compliance Receiving Report for raw materials and packaging components, in accordance with internal and external regulations and policies, to meet supply chain cycle time goals.
  • Maintains accurate and orderly records of all work performed and collaborates with the Technical Development group during product validation activities and the transfer of new products.
  • Assigns appropriate disposition to materials/products through the Computer System within established cycle time and schedules.
  • Verifies (Peer Reviewer) data/results generated by another Incoming Inspector.
  • Maintains and controls documents in safe files, ensuring the protection of active records.
  • If the associate acts as an Environmental Trainer Auditor, the following responsibilities apply:
  • Acts as an OMP ISO 14001 Team Member, supporting the Environmental Management System Coordinator in the implementation, training, and continuous improvement of the EMS in their operational area and any other activities where required.
  • Conducts monthly environmental audits in their operational area.
  • Provides environmental talks on a bi-monthly basis to their operational area.
  • Conducts weekly inspections of chemical cabinets in their operational area.
  • Provides assistance in conducting semi-annual Environmental Management System audits at the JSC-Gurabo site.

We are searching for the best talent for QC Incoming Inspector.

Purpose: The Quality Incoming Inspector is responsible for the sampling, inspection, and approval of packaging components, as well as the testing of both packaging components and some raw materials. Ensure compliance with all quality control policies, procedures, and systems to facilitate the timely release of high-quality products that support the supply chain process. It is essential to perform functions effectively to avoid potential consequences such as product recalls, production delays, and backorder status.

What you need

3 ways to qualify

  1. Bachelor’s

    + 0–2 years of experience

    Bachelor’s Degree in Natural Science, preferably with a major in Biology or Chemistry, and 0–2 years of experience in a pharmaceutical GMP environment is required; or

  2. or

    Associate

    + 2–4 years of experience

    Associate’s Degree in Natural Science and 2–4 years of experience in a pharmaceutical GMP environment is required; or

  3. or

    High school

    + 4+ years of experience

    High School Diploma and a minimum of 4 years of experience in a pharmaceutical GMP environment is required.

Qualifications / Requirements

  • Knowledge of cGMPs and safety regulations is required.
  • Fluent in both Spanish and English is required.
  • Basic computer, software knowledge, and word processing is required.
  • Knowledge use ANSI Inspectors Rule is required.
  • Knowledge of Product & Body function is preferred.
  • Availability to work 1st, 2nd, 3rd, and 12-hour shifts, including overtime, weekends, and holidays is required.

Johnson and 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, please email the Employee Health Support Center ([email protected]) or contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.

Preferred Skillsnice to have

Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

Where you'll work

Gurabo, PROn-siteOpen in Maps (opens in a new tab)

More jobs in Gurabo, PR

Working conditions

Job Function

Quality

Job Sub Function

Quality Control

Job Category

Professional

All Job Posting Locations

Gurabo, Puerto Rico, United States of America

Smiling Johnson & Johnson employees waving from red picnic blankets on the lawn at J&J Day

From the posting

About Johnson & Johnson

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Johnson & Johnson company page · 45 open roles
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word

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.

Job intelligence

The context around this role

Live data · October 28, 2026

Salary intelligence

How the pay compares

Associate & Specialist roles in the US130 roles publishing pay

Middle half $49,125 to $78,500, median $61,250
Annual base pay
Annual base payLowMedianHigh
All US$49,125$61,250$78,500

Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Inspector · Quality Control Inspector

    $61K median192 open
  2. Next step

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $96K median88 open
  3. Later

    Manager

    Often: Supervisor, Quality Control · Manager, Quality Control

    $112K median36 open
  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $198K median25 open

Skills DNA

What this role leans on

How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 13 linesLab testing and methods: 4 linesDocumentation and SOPs: 6 linesValidation and qualification: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 2 linesData and digital systems: 2 linesCollaboration and leadership: 3 linesGMPLab testingDocumentationValidationSubmissionsQuality systemsData systemsTeamwork
  • GMP and compliance13
  • Documentation and SOPs6
  • Lab testing and methods4
  • Collaboration and leadership3
  • Quality systems and risk2
  • Data and digital systems2
  • Validation and qualification1
  • Regulatory submissions1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

Johnson & Johnson on Regulatory Jobs

45
Open roles
44
Distinct roles
22
Locations

By discipline

  • Quality31 69%
  • Regulatory11 24%
  • Compliance & Safety3 7%

By level

  • Associate & Specialist16 36%
  • Senior & Principal15 33%
  • Manager11 24%
See all 45 Johnson & Johnson roles

More roles at Johnson & Johnson

All 45 Johnson & Johnson roles

Similar Quality Control roles elsewhere

QC Incoming Inspector at Johnson & Johnson

Applications close November 2.

Job alerts