Johnson & Johnson Innovative Medicine Hiring QC Specialist – Apply Now!
Johnson & Johnson Innovative Medicine is seeking a dedicated QC Specialist – Lab Services for its Raritan, New Jersey facility. This full-time position is ideal for candidates with a Bachelor’s degree in Biology, Chemistry, Biochemistry, Microbiology, or a related field, and a minimum of 2 years’ experience in pharmaceutical or biopharma QA/QC environments. This role involves sample management, compliance with cGMPs, documentation review, and regulatory audit support—offering a competitive salary range of $59,000 to $74,000 annually.
About Johnson & Johnson Innovative Medicine:
Johnson & Johnson Innovative Medicine, a part of Johnson & Johnson, is at the forefront of creating life-changing treatments through science and innovation. With a focus on complex diseases and patient-driven solutions, J&J is dedicated to delivering smarter, less invasive, and more personalized therapies. The Raritan, NJ site plays a pivotal role in its mission to profoundly impact health for humanity.
About the Job
Job Post: Quality Control (QC) Specialist
Job Location: Raritan, NJ
Job Category: Quality Control – Professional
Sub Function: Lab Services
Salary Range: $59,000 – $74,000 annually
Work Hours: May include weekends and evenings
Job Description
Purpose: The QC Specialist, Lab Services, is responsible for sample management. The QC Specialist is encouraged to work independently on routine tasks and have a conceptual understanding of all Quality Control functions and business areas. They will serve as a technical specialist within the job function.
You Will Be Responsible For
- Prepares and reviews documentation independently.
- Responsible for QC sample and retention management.
- Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems.
- Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and lab management software system (LIMS).
- Prepare documents and coordinate sample shipments (both internal and external).
- Review logbooks and/or LIMs to ensure the physical quantities of samples in freezers are aligned.
- Periodic inspection and consolidation of retaining walls.
- Document and perform sample management-related non-conformance investigations.
- Document and handle corrective and preventive action records.
- Supports internal and regulatory audits.
- Conduct an annual off-site visual inspection of the retaining walls.
Qualifications / Requirements
- Minimum of a Bachelor’s or equivalent University degree with a focused degree in Biology, Biochemistry, Microbiology, Chemistry, or related field preferred.
- Minimum of two (2) years related experience in the medical device, biopharmaceutical, or pharmaceutical industry.
- Ability to accommodate weekend and evening work as required by the manufacturing process.
Preferred Qualifications
- Solid understanding of regulatory requirements, policies, and guidelines.
- Experience with Quality Control document reviews and regulatory inspection processes.
- Working knowledge of Quality systems.
- Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint), and LIMS.
Additional Information
This position may require up to 10% domestic travel. Occasional heavy lifting up to 20 pounds may be required.
The anticipated base pay range for this position is $59,000 to $74,000.
Keywords: Johnson & Johnson, QC Specialist, Lab Services, Raritan, New Jersey, Healthcare, Quality, Innovative Medicine
