Ethicon, a member of the Johnson Johnson Family of Companies, is recruiting for a Quality Assurance Technician located in its manufacturing site at San Lorenzo, Puerto Rico.

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 https://www.jnj.com/. 

The Quality Assurance Technician reports to the Quality Team Leader or Designee, with the objective of maintaining high Quality Standards for Product Quality Control and operations compliance with regulatory requirements. Conducts routine physical inspection procedure to in-process material, as well as finished goods, as needed. Inspection involves the use of skilled specifications and established quality standards. Performs audits to ensure product and processes comply with requirements.

Responsibilities:

Maintains high Quality Standards for Product Quality Control and operations compliance with regulatory requirements.Conducts routine physical inspection, testing, or evaluation to ensure quality of products according to current specifications/procedures.Performs product and process audits.Notify any product or process non-conformance and escalates as appropriate.Segregates and inspects Finished Goods samples and Retain Samples according to the requirements. Delivers samples to Finished Goods QA Lab if needed.Performs data analysis and executes final disposition of the material as required.Performs batch records review accordingly with compliance requirements and complete record retention process.Maintain knowledge of all procedures, change to specifications and new regulations related to their areas of responsibility.Support associates on defect awareness and specifications requirements.Support validation activities as required.Comply with the OPCERT program for the certification of manufacturing associates.Evaluate and approve control and disposition of material to determine if it is according to the requirements and Quality System Regulations.

Ethicon, a member of the Johnson Johnson Family of Companies, is recruiting for a Quality Assurance Technician located in its manufacturing site at San Lorenzo, Puerto Rico.

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 https://www.jnj.com/. 

The Quality Assurance Technician reports to the Quality Team Leader or Designee, with the objective of maintaining high Quality Standards for Product Quality Control and operations compliance with regulatory requirements. Conducts routine physical inspection procedure to in-process material, as well as finished goods, as needed. Inspection involves the use of skilled specifications and established quality standards. Performs audits to ensure product and processes comply with requirements.

Responsibilities:

Maintains high Quality Standards for Product Quality Control and operations compliance with regulatory requirements.Conducts routine physical inspection, testing, or evaluation to ensure quality of products according to current specifications/procedures.Performs product and process audits.Notify any product or process non-conformance and escalates as appropriate.Segregates and inspects Finished Goods samples and Retain Samples according to the requirements. Delivers samples to Finished Goods QA Lab if needed.Performs data analysis and executes final disposition of the material as required.Performs batch records review accordingly with compliance requirements and complete record retention process.Maintain knowledge of all procedures, change to specifications and new regulations related to their areas of responsibility.Support associates on defect awareness and specifications requirements.Support validation activities as required.Comply with the OPCERT program for the certification of manufacturing associates.Evaluate and approve control and disposition of material to determine if it is according to the requirements and Quality System Regulations.High School Diploma and one (1) year of experience in a regulated industry is required; or Bachelor’s Degree in a technical or science field is required.One (1) year of quality assurance experience is preferred.Knowledge of QSR's and ISO Standards is preferred.Verbal and written communication skills in English and Spanish are required.PC literacy including MS Office and use of other software and applications is requiredAnalytical and problem-solving skills are required.Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and/or 12-hour daily shifts, including weekends and holidays is required.

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belong.

High School Diploma and one (1) year of experience in a regulated industry is required; or Bachelor’s Degree in a technical or science field is required.One (1) year of quality assurance experience is preferred.Knowledge of QSR's and ISO Standards is preferred.Verbal and written communication skills in English and Spanish are required.PC literacy including MS Office and use of other software and applications is requiredAnalytical and problem-solving skills are required.Availability to work overtime, various work schedules, which may include 1st, 2nd, 3rd shifts and/or 12-hour daily shifts, including weekends and holidays is required.

For more than 130 years, diversity, equity inclusion (DEI) has been a part of our cultural fabric at Johnson Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson Johnson, we all belong.