- Job title QC Analyst (Analytical Instrument and Lab Systems)
- Function Quality
- Sub function Quality Control
- Category Experienced Analyst, Quality Control (P5)
- Location Wilson / United States of America
- Date posted
- Requisition number R-029184
- Work pattern Fully Onsite
This job posting is anticipated to close on Sep 03 2025. 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 https://www.jnj.com
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 Large Molecule Drug Substance Manufacturing facility in Wilson North Carolina (BioNC). In this key role, you will be responsible for laboratory equipment lifecycle management and CSV support, 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 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.
- Author SOP’s, Work Instructions and protocols.
- Responsible for the quality control laboratory equipment lifecycle management and CSV support.
- Participate in activities to introduce technologies and computer base applications to a new site, for example eLIMS/iLABS, SDMS, Empower and SoftMax Pro, to improve laboratory efficiency and promote a culture of Innovation.
- Interact with the QC Global organization for the different center of excellence for equipment and information technologies.
- 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 4+ 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.
- Working knowledge of laboratory systems.
- Strong technical knowledge in and experience with QC analytical equipment is required.
- 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.