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Analyst 1, Chemistry Lab Jobs
Company | Johnson & Johnson |
Address | San Angelo Area, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-08-04 |
Posted at | 10 months ago |
- Able to work in an environment with chemicals safely.
- Recommends and implements revisions, corrections and changes to test equipment, procedures and methods.
- Performs raw material, in-process and/or finished goods tests and reviews.
- Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001)
- Completes record of inspection results, acceptance, rejection and disposition for entry into logbooks or computer systems (i.e. LIMS).
- Performs chemical and sterility release of product.
- Carries out difficult calculations and prepares documentation that shows the results for the test performed.
- Monitors and reviews environmental charts and/or numeric data.
- Support process improvement teams for departmental and company continuous improvement activities (Lean, compliance laboratory processes, etc.)
- Conducts training for lower level technicians and operations.
- Execute simple microbiology analyses in-process sample and finish products (Microbial count, Environmental Monitoring and sterility test) to comply with current procedures and Pharmacopoeias.
- Initiates and coordinates discussions with quality, engineering and other relevant departments to develop corrective actions for reoccurring problems
- Performs sterility, environmental, moisture, residual ethylene oxide, and triclosan testing.
- Responsible to ensure adequate systematic control of nonconforming product.
- Cross-trains to support other functional areas.
- Ensures proper safety and environmental procedures and practices are utilized
- Basic Technical writing techniques knowledge to perform preliminary laboratory investigation.
- Experience on proper use and basic troubleshooting on the following laboratory instrumentations: UPLC, HPLC, GC, FTIR, pH, KF, Particle counter, RCS.
- Performs other duties assigned as by any member of Laboratory Management.
- Investigate and write out of specification reports.o Read and interpret results, performs trend analysis as required.
- Participates on special requests for product testing, such as qualification protocols
- Inspects, tests and/or evaluates the precision and accuracy of products, and/or testing equipment.
- Prepares media and performs quality assurance control checks per USP.
- Basic knowledge on microbiology principles, theories, practices and methodology.
- Recommends, amends and analyzes sampling procedures, test methods, standard operating procedures, and/or inspection measures in order to lean processes or simplify current practices.
- 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 (theorical and practical) to evaluate and troubleshoot chromatography analysis, document and review chromatography and/or spectroscopy (GC, UPLC, HPLC, FTIR, etc.) results that could impact the results for the test performed.
- Demonstrated knowledge and expertise in quality processes and regulatory requirements.
- Basic wet chemistry techniques related to qualitative and quantitative
- Good interpersonal relations and communication skills required
- University / Bachelor’s Degree or Equivalent is required with major on Science preferred
- Knowledge of Microsoft Office, LIMS, Empower and other computer software recommended
- Generally Requires 0-2 Years Work Experience
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