Johnson Johnson is currently seeking a QC Associate Analyst located in Malvern, PA.

There is an internal pre-identified candidate for consideration. However, all applications will still be reviewed.

About Johnson Johnson

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/.

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.

Job Summary

The QC Associate Analyst conducts biochemical, microbiological, and/or general chemical testing of raw material, in-process, or final product samples submitted to the QC laboratories. The position requires testing to be completed in compliance with all applicable procedures, standards and GMP regulations

Principal Responsibilities

Perform analytical testing in compliance with all applicable procedures and GMP regulationsMaintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations

Analytical Testing (70%)

Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratoriesPerform peer review of laboratory dataUtilize electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing

Laboratory Support (20%)

General housekeepingSample and reference standard managementInstrument Calibration and/or Preventative MaintenanceTraining new laboratory personnelUpdate QC documents using the Document Management SystemSupply ordering/receipt

Quality Compliance (5%)

Maintain individual training completion in a compliant stateComplete invalid assay investigation recordsComplete corrective and preventative actions (CAPA) as assigned

Projects/Meetings (5%)

Provide input to functional laboratory meetingsParticipate on and make contributions to continuous improvement teams

Johnson Johnson is currently seeking a QC Associate Analyst located in Malvern, PA.

There is an internal pre-identified candidate for consideration. However, all applications will still be reviewed.

About Johnson Johnson

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/.

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.

Job Summary

The QC Associate Analyst conducts biochemical, microbiological, and/or general chemical testing of raw material, in-process, or final product samples submitted to the QC laboratories. The position requires testing to be completed in compliance with all applicable procedures, standards and GMP regulations

Principal Responsibilities

Perform analytical testing in compliance with all applicable procedures and GMP regulationsMaintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations

Analytical Testing (70%)

Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratoriesPerform peer review of laboratory dataUtilize electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing

Laboratory Support (20%)

General housekeepingSample and reference standard managementInstrument Calibration and/or Preventative MaintenanceTraining new laboratory personnelUpdate QC documents using the Document Management SystemSupply ordering/receipt

Quality Compliance (5%)

Maintain individual training completion in a compliant stateComplete invalid assay investigation recordsComplete corrective and preventative actions (CAPA) as assigned

Projects/Meetings (5%)

Provide input to functional laboratory meetingsParticipate on and make contributions to continuous improvement teamsBA/BS Degree Scientific or related field0-2 years of Laboratory related experienceBasic knowledge of analytical technologies used in the QC laboratorySkilled in performing basic testing within the functional laboratoryExperience using Good Laboratory Practices (GLP) and basic knowledge of current Good Manufacturing Practices (cGMP) related to the QC laboratoryAbility to read and interpret documents such as SOPs, work instructions, test methods and protocolsProficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)Makes GMP decisions primarily under the guidance of QC supervisionPerforms basic troubleshooting and works directly with supervision for problem resolutionInnovation/Creativity is typically not required for effectively performing the job. The QC Associate Analyst shall have the capability to develop improvement ideas but may not necessarily be required to implement the associated solutions.Frequently requires supervisory guidance/directionMay have basic influencing skills

Physical Requirements:

Required to work with chemical and biological substances on a daily basisRequired to work on feet or seated for extended periods of time in a laboratory settingRequires sufficient vision to adequately perform visual inspections of materials (color, appearance, particles, etc.) and to document observations during laboratory testingOccasionally required to lift up to 20 poundsInfrequently (< 5%) required to travel to other sites/locations

There is an internal pre-identified candidate for consideration. However, all applications will still be reviewed.

Johnson Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

BA/BS Degree Scientific or related field0-2 years of Laboratory related experienceBasic knowledge of analytical technologies used in the QC laboratorySkilled in performing basic testing within the functional laboratoryExperience using Good Laboratory Practices (GLP) and basic knowledge of current Good Manufacturing Practices (cGMP) related to the QC laboratoryAbility to read and interpret documents such as SOPs, work instructions, test methods and protocolsProficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)Makes GMP decisions primarily under the guidance of QC supervisionPerforms basic troubleshooting and works directly with supervision for problem resolutionInnovation/Creativity is typically not required for effectively performing the job. The QC Associate Analyst shall have the capability to develop improvement ideas but may not necessarily be required to implement the associated solutions.Frequently requires supervisory guidance/directionMay have basic influencing skills

Physical Requirements:

Required to work with chemical and biological substances on a daily basisRequired to work on feet or seated for extended periods of time in a laboratory settingRequires sufficient vision to adequately perform visual inspections of materials (color, appearance, particles, etc.) and to document observations during laboratory testingOccasionally required to lift up to 20 poundsInfrequently (< 5%) required to travel to other sites/locations

There is an internal pre-identified candidate for consideration. However, all applications will still be reviewed.

Johnson Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.