This job posting is anticipated to close on May 18 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:
ProfessionalAll Job Posting Locations:
Wilson, North Carolina, United States of AmericaJob Description:
We are currently seeking a highly qualified individual to join our team as a QC Analyst (Analytical Instrument and Lab Systems) at our new Biotherapeutics Manufacturing facility in Wilson, North Carolina (BioNC). In this key role, you will be responsible for laboratory equipment lifecycle management, CSV support, and introducing & maintaining lab systems, among others.
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
Essential Job Duties and Responsibilities:
Participate in activities to introduce and sustain eLIMS at a new site, including user requirements support, master data setup/maintenance (tests, specifications, products, instruments, reagents), workflow configuration, user access/role administration, interface coordination (e.g., instruments/SDMS), and go-live readiness activities (UAT support, training, cutover planning) to improve laboratory efficiency and promote a culture of innovation.
Author SOP’s, Work Instructions and protocols.
Responsible for the quality control laboratory equipment lifecycle management and CSV support.
Interact with the QC Global organization for the different center of excellence for equipment and information technologies.
Participate in the qualification of analytical equipment for related testing functions, for example, IQ/OQ/PQ of HPLC, Spectrophotometry, Endotoxin, Cell Culture and Total Organic Carbon equipment.
The resolution of unexpected complex compliance or lab instrument and system issues as they arise
Qualifications:
Bachelor’s Degree in Chemistry, Biochemistry, Micro or science related field with 2+ years related experience in biopharmaceutical or pharmaceutical industry. And/or an equivalent combination of education and experience.
Working knowledge of regulatory requirements, policies and guidelines. Experience with Quality Control document reviews and regulatory inspection processes.
Strong technical knowledge of laboratory systems/eLIMS is required. Knowledge of the eLIMS LabVantage system is preferred.
Working knowledge in and experience with QC analytical equipment.
Knowledge of cGMP regulations and FDA/EU guidance is required.
Other Requirements:
An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.
Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and communicate complex quality concepts to stakeholders at all levels.
Proven ability to manage multiple priorities and work independently with minimal supervision.
Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.
Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.
The ability to work in a team environment and interact with all levels of the organization.
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, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
#Onsite
Required Skills:
Preferred Skills:
