
Job Information
J&J Family of Companies Technical Expert Analytical Instrument and Lab Systems in Wilson, North Carolina
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:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Wilson, North Carolina, United States of America
Job 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 currently seeking a highly qualified individual to join our team as a Technical Expert Analytical Instrument and Lab Systems at our new Large Molecule Drug Substance Manufacturing facility in Wilson, North Carolina. In this key role, you will be responsible for laboratory equipment lifecycle management and CSV support, among others.
J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience. J&J’s significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.
Key Responsibilities:
Responsible for the quality control laboratory equipment lifecycle management and CSV support.
Participate in the qualification of analytical equipment for related testing functions, for example HPLC, Spectrophotometry, Endotoxin, Cell Culture and Total Organic Carbon.
Participate in activities to introduce new products, technologies and computer base applications to improve laboratory efficiency and promote 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:
Education
- Bachelor’s Degree in Science or Engineering related field is required.
Experience and skills
Required
A minimum of 4 years of related work experience in biopharmaceutical or pharmaceutical industry.
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.
Knowledge of cGMP regulations and FDA/EU guidance.
Preferred
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.
Note: This position description is a general guideline; it does not purport to be an exhaustive list of all elements of the position. Management reserves the right to modify this position description at any time, or to vary the duties and responsibilities of the position to meet production, scheduling or other business needs.
If you are passionate about quality in the pharmaceutical industry and possess the necessary skills and experience, we invite you to apply for this exciting opportunity as a Technical Expert Analytical Instrument and Lab Systems. Join our team and contribute to the development of life-saving therapies in a dynamic and rewarding environment.
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 and 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 email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
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