Laboratory Analyst 1 Quality Control
Date de publication :
30 septembre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :San Angelo
Johnson & Johnson is currently seeking a Laboratory Analyst 1 Quality Control to join Ethicon located in San Angelo, TX.
About Johnson & Johnson
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Summary
Responsible for conducting complex test and analysis to assure that product comply with established specifications.
Duties and Responsibilities
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
- Performs raw material, in-process and/or finished goods tests and reviews.
- Able to work in an environment with chemicals safely.
- Inspects, tests and/or evaluates the precision and accuracy of products, and/or testing equipment.
- Monitors and reviews environmental charts and/or numeric data.
- Performs chemical and sterility release of product.
- Performs sterility, environmental, moisture, residual ethylene oxide, and triclosan testing.
- Carries out difficult calculations and prepares documentation that shows the results for the test performed.
- Prepares media and performs quality assurance control checks per USP.
- Investigate and write out of specification reports.
- Read and interpret results, performs trend analysis as required.
- Recommends, amends and analyzes sampling procedures, test methods, standard operating procedures, and/or inspection measures in order to lean processes or simplify current practices.
- Performs other duties assigned as by any member of Laboratory Management.
- Execute simple microbiology analyses in-process sample and finish products (Microbial count, Environmental Monitoring and sterility test) to comply with current procedures and Pharmacopoeias.
- Basic knowledge on microbiology principles, theories, practices and methodology.
- Basic Technical writing techniques knowledge to perform preliminary laboratory investigation.
- Completes record of inspection results, acceptance, rejection and disposition for entry into logbooks or computer systems (i.e. LIMS).
- Support process improvement teams for departmental and company continuous improvement activities (Lean, compliance laboratory processes, etc.)
- Responsible to ensure adequate systematic control of nonconforming product.
- Recommends and implements revisions, corrections and changes to test equipment, procedures and methods.
- Experience on proper use and basic troubleshooting on the following laboratory instrumentations: UPLC, HPLC, GC, FTIR, pH, KF, Particle counter, RCS.
- Participates on special requests for product testing, such as qualification protocols
- Initiates and coordinates discussions with quality, engineering and other relevant departments to develop corrective actions for reoccurring problems
- Conducts training for lower level technicians and operations.
- Cross-trains to support other functional areas.
- Ensures proper safety and environmental procedures and practices are utilized
- Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).
- The San Angelo Plant is a 24/7 operation; weekends and holidays are included in the work schedule.
- Due to the nature of the San Angelo plant operation, there will be times that working outside your standard working hours will be expected and/or mandatory to ensure there is no interruption in the business performance. All such time will be compensated according to local law and procedures