This job posting is anticipated to close on Jul 22 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 AssuranceJob Category:
ProfessionalAll 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 a Quality Systems Specialist Complaints to be located in Gurabo, PR.
The Quality Systems Specialist – Complaints is responsible for ensuring that the handling of complaints complies with established company and corporate standard operating procedures, policies, rules, and regulations, as well as current Good Manufacturing Practice (GMP) guidelines.
Key Responsibilities:
Collaborates with the Operations Department to facilitate the investigation of customer complaints.
Conducts physical field sample receiving activities, including decontamination if necessary.
Analyzes data to generate weekly metrics for the Quality System Complaints Department.
Utilize statistical techniques to track and analyze processes.
Edits, reviews, and approves QA System documentation, such as Work Instructions, Standard Operating Procedures, Reports, and forms, as required.
Actively participates in projects, programs, safety and environmental training, cGMP, SOPs, and other activities to foster employee involvement and professional development.
Escalate issues to the Site Quality Head, Senior Manager, and/or the Complaint Lead of the Quality Assurance unit.
Actively engages in Credo initiatives.
Proactively seeks improvements and welcomes new assignments.
Support regulatory inspections by providing subject matter expertise and assisting with data gathering and evaluations.
Participate regularly with management team to identify solutions to common issues and prioritize solutions.
Qualifications:
A bachelor’s degree in engineering or a Science field such as Pharmacy, Chemistry, Biology, or a related discipline is required. An MA/MS/MBA or a related science degree is desirable.
A minimum of 1 to 2 years of experience in Quality Complaint Investigation process in the pharmaceutical industry, preferably in QA compliance areas, with comprehensive knowledge and understanding of domestic and international guidelines, cGMPs, pharmaceutical manufacturing and packaging, and quality control activities for various dosage forms is required.
Professional experience in Quality Assurance, Regulatory Compliance, or other related areas within a highly regulated industry, such as pharmaceuticals, food and dairy processing, or medical devices, is required.
A thorough understanding of FDA regulations and requirements applicable to drug products, as well as international regulatory requirements, is essential.
Extensive knowledge of cGMPs and compliance standards is required.
Excellent technical writing skills, including the ability to organize information in a logical and coherent manner.
Excellent oral and written communications skills and fully bilingual in both English and Spanish.
Expert understanding of cGMP, Good Documentation Practices, and Regulations.
Expertise in JSC document management and change control 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.
Required Skills:
Preferred Skills:
