Job 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

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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

We are currently seeking a highly qualified individual to join our team as a QC Lab Support/System Specialist at our new Large Molecule Drug Substance Manufacturing facility located in Wilson, North Carolina.

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. 

In this key role, the QC Lab Support/System Specialist is responsible for the Quality Control laboratory services support including lab documentation management, material/supplies purchase, eLims support, among others. 

Key Responsibilities:

• Responsible for the Quality Control laboratory services support including Lab documentation management, material/supplies purchase, eLims support, among others.
• Perform QC project activities to introduce new products, technologies and computer base applications to BioNC to improve laboratory efficiency and promote culture of Innovation.
• Maintain the Quality metrics program, to ensure and proactively enhance compliance and business performance of the site.
• Find resolution to unexpected complex compliance or quality system issues as they arise
• Keep abreast of regulatory changes and industry best practices related to laboratory services.
• Coordinates/Assists in the pick-up of samples and deliveries to the laboratories/ Receives samples in the laboratory systems when necessary
• Services orders for the purchasing, receiving and organizing of laboratory supplies and reagents.

Qualifications:

Education

• Bachelor’s Degree in a science or engineering related field is required.

Experience and skills

Required

• A minimum of 2 years of related 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 Quality systems.

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 QC Lab Support/System Specialist. 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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