About Us:
At Johnson & Johnson, we are committed to delivering excellence in every aspect of our operations. We adhere to strict federal, state, and local regulations, as well as corporate guidelines to guarantee the highest quality of our products. We're seeking a talented Quality Control Laboratory Technician to join our team and contribute to our commitment to quality and safety.
What You'll Do:
As a Quality Control Laboratory Technician, you will play a vital role in ensuring the quality and safety of our products. Your responsibilities will include:
- Testing and Inspection: Perform raw material, in-process, and finished goods tests and reviews to assess precision and accuracy. This includes inspecting, testing, and evaluating products and testing equipment.
- Environmental Monitoring: Monitor and review environmental charts and numeric data to ensure compliance with standards.
- Microbiology: Execute microbiology analyses on in-process samples and finished products, including microbial counts, environmental monitoring, and sterility tests.
- Documentation: Prepare thorough documentation of test results, calculations, and quality control checks. This includes trend analysis and the preparation of media per USP standards.
- Continuous Improvement: Collaborate with process improvement teams to enhance departmental and company processes, such as Lean and compliance laboratory processes.
- Troubleshooting: Utilize your knowledge of laboratory instrumentation, including UPLC, HPLC, GC, FTIR, pH, KF, particle counters, and RCS, to troubleshoot and maintain equipment.
- Quality Assurance: Ensure systematic control of nonconforming products and recommend revisions, corrections, and changes to procedures and methods.
- Training: Conduct training for lower-level technicians and operations, promoting skill development and knowledge sharing.
- Safety: Adhere to proper safety and environmental procedures, promoting a culture of safety within the laboratory.
Basic Qualifications:
- A Bachelor's Degree or Equivalent with a major in a Science field is required.
- 0-2 years of work experience.
- Strong interpersonal and communication skills.
- Knowledge of Microsoft Office, LIMS, Empower, and other relevant computer software.
- Demonstrated expertise in quality processes and regulatory requirements.
- Experience working in an FDA regulated environment (21 CFR Part 211 and 211, 21 Part 820, ICH Q7, and/or 21 CFR Part 4).
- Basic Spectroscopy knowledge (theoretical and practical) to evaluate and troubleshoot chromatography analysis.
- Familiarity with wet chemistry techniques related to qualitative and quantitative analysis.
Why Join Us:
- Be part of a company committed to excellence and safety.
- Contribute to the quality assurance of life-saving products.
- Collaborate with a dedicated team of professionals in a dynamic environment.
- Competitive compensation and opportunities for growth and development.
If you're excited to be part of a team that upholds the highest standards in quality and safety, we want to hear from you. Apply today and join us in our mission to ensure product excellence!