QC Incoming Inspector

Johnson & Johnson Co.; Gurabo (PR); Presencial; USD 42.000 - 64.000; Jornada completa

Descripción de la vacante

Johnson & Johnson is seeking an QC Incoming Inspector in Gurabo, Puerto Rico, to sample, inspect, and approve packaging components and some raw materials for release in a GMP environment. The role emphasizes compliance with quality systems and timely cycle times to protect the supply chain.

Responsibilities include reviewing COA/CoC, maintaining records, and collaborating with product validation teams. Flexibility for 1st-3rd shifts is required, with regulatory knowledge and strong bilingual

Formación

• Bachelor’s degree in natural science with biology or chemistry is preferred; 0–2 years GMP experience required.
• Associate’s degree in natural science with 2–4 years GMP experience required.
• High School Diploma with at least 4 years GMP experience required.

Responsabilidades

• Performs sampling, inspection, testing, and approval of packaging components per regulations.
• Performs sampling and testing of raw materials per regulations.
• Inspects labeling, quantity, and materials or products to be shipped.
• Maintains the Retention Room orderly.
• Audits COA and COC Receiving Report for materials.
• Maintains records and collaborates with Technical Development during validation and transfers.
• Assigns disposition in the Computer System within cycle time.
• Verifies peer data/results.
• Maintains controlled documents in safe files.
• If Environmental Trainer Auditor: acts as EMS team member and conducts audits.
• Conducts environmental talks and weekly inspections of chemical cabinets.

Conocimientos

Spanish & English fluency

cGMP knowledge

Safety regulations knowledge

Basic computer skills

ANSI Inspectors Rule knowledge

Shift work availability

Educación

Bachelor’s Degree in Natural Science (Biology or Chemistry)

Associate’s Degree in Natural Science

High School Diploma with GMP experience

Herramientas

Word processing software

Descripción del empleo

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 Control

Job Category

Professional

All Job Posting Locations

Gurabo, Puerto Rico, United States of America

Job Description

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

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.

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.

Qualifications / Requirements

• 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
• Associate’s Degree in Natural Science and 2–4 years of experience in a pharmaceutical GMP environment is required; or
• High School Diploma and a minimum of 4 years of experience in a pharmaceutical GMP environment is required.
• 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 & 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 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 ([e-mail]) 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 Skills

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