This job posting is anticipated to close on Sep 02 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.
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:
QualityJob Sub Function:
Quality ControlJob Category:
Business Enablement/SupportAll Job Posting Locations:
Gurabo, Puerto Rico, United States of AmericaJob 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 Coordinator located in Gurabo, PR.
The QC Incoming Coordinator is responsible for sampling, inspecting, and approving Packaging Components. Also responsible for testing Packaging Components and some Raw Materials.
The Coordinator must ensure compliance with all quality control policies, procedures, and systems to facilitate the timely release of high-quality products to support the supply chain process. Failure to effectively perform their functions may lead to product recall, production delays, and/or back-order status.
Key Responsibilities:
Coordinates and executes (when necessary) sampling, inspection, testing, and approval activities of Packaging Components in accordance with internal and external regulations, policies, and supply chain cycle time goals.
Ensures that the sampling and testing of Raw Materials is performed in compliance with internal and external regulations, policies, and supply chain cycle time goals.
Coordinates and executes (when necessary) the inspection of labeling, quantity, and material or product to be shipped.
Maintains a well-organized Retention Room.
Audits the Certificate of Analysis and Certificate of Compliance Receiving Report of Raw Materials and Packaging Components in accordance with internal and external regulations, policies, and supply chain cycle time goals.
Keeps accurate and organized records of all work performed.
Collaborates with the Technical Development group during the validation activities and transfer of new products.
Assigns appropriate disposition to materials/products through the Computer System within established cycle time and schedules.
Verifies data/results generated by another Incoming Inspector as a Peer Reviewer.
Maintains and controls documents in safe files, ensuring that active records are protected.
Comply with the goals of the quality team and overall business and process goals.
Follows Safety and Environmental procedures in all areas.
Adheres to the principles of conduct expressed in the Company Credo and policies.
Coordinates and performs other duties as necessary to support the supply chain process.
Support Internal and External Audit process as applicable.
As an Environmental Trainer Auditor, the following responsibilities apply:
Acts as a member of the OMP ISO 14001 Team, providing support to the Environmental Management System Coordinator in implementing, training, and improving the EMS in their operational area and other required activities.
Conducts monthly environmental audits in their operational area.
Delivers environmental talks to their operational area on a bi-monthly basis.
Conducts weekly inspections of chemical cabinets in their operational area.
Assists in conducting semi-annual Environmental Management System audits at the Gurabo site.
Qualifications:
A minimum of an Associate Degree or BS Natural Sciences (with a major in Biology or Chemistry preferably) is required.
A minimum of 6 years of experience in pharmaceutical GMP Environment is required, preferable in the Incoming Area.
Availability to provide support by working in external locations as per business needs is required.
Knowledge of SAP, eLIMS applications is preferred
Forklift certification is desired.
Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and/or other work shifts, including weekends and holidays.
This position may require up to a 10% of domestic and/or international travel.
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.
Required Skills:
Preferred Skills:
Communication, Compliance Management, Execution Focus, ISO 9001, Problem Solving, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Standard Operating Procedure (SOP), Teamwork, Technologically Savvy