You are successfully logged out of your my randstad account

You have successfully deleted your account

finished product quality assurance.

detalles del trabajo

resumen

    detalles del trabajo

    ¡Esta propuesta te puede interesar!

    En Randstad nos moviliza ayudar a las personas y a las organizaciones a desarrollar todo su potencial. Ese es el compromiso que asumimos como compañía en todo el mundo, un compromiso que nos impulsa a ir más allá para lograr que nuestros clientes y candidatos alcancen el éxito. ¿Cómo lo hacemos?, combinando nuestra pasión por las personas con el poder de la tecnología, creando experiencias más humanas, que nos permitan ser una fuente de inspiración y apoyo para quienes nos eligen. Porque estamos convencidos de que mejores personas hacen mejores empresas.

     

    From our Healthcare & Life Science division, we are looking for an Important Multinational Pharmaceutical Company, for a Physical Chemical Analyst for product quality control, in the area of Pilar.

    Key Tasks & Responsibilities:

    • Adhere to all aspects of Corporate and Plant safety programs, GMP’s, ISO standards or other regulatory requirements.

    • Perform and support standard qualitative and quantitative analysis on in-process products, packaging components, bulk and finished products in accordance with the approved testing procedures.

    • Adhere to Regulatory guidelines for documentation, ensuring accurate, clear, legible and complete records of all information related to the sample login and release, analytical testing and investigations, preventive maintenance and instrument calibration, inventory and training.

    • Trained/qualified on basic and various analytical techniques, instruments and equipment, for qualitative and/or quantitative analysis.

    • Prepare laboratory reagent solutions for in process and finished products per monograph procedures as needed to support the laboratory. Prepare sample placebos for method development and validations.

    • Perform glassware washing to support the laboratory. Distribute and maintain adequate levels of clean glassware as required for testing needs. 

    • Prepare and file retain samples for bulk products. Maintain the sample file room. Manage the monthly retains for all tested samples.

    • Responsible for filing the laboratory documentation and the review of the laboratory documentation prior to filing.

    • Update the records for testing procedures and monographs when revised or replaced. Responsible for returning the obsolete monographs to QA.

    • Assist supervisor with revising SOPs, testing procedures and training material, with non-compliance investigations for in-process work and other special assignments as directed.

    • Participate in laboratory safety audits and solvent dumping schedule.

    • Participate in QC weekly PSS dialogue.

    • May perform other duties as assigned, including housekeeping tasks.

    Qualifications and Competencies: 

    • University degree (Chemical, Biotechnology, Physico-Chemical) or advanced degree in science/ engineering.

    • At least 3 years of GMP Lab experience required, showing demonstrated ability to accurately conduct routine QC tests in accordance with approved written procedures and demonstrated ability to follow production schedule with minimal direction from her/ his manager.

    • Demonstrated ability to give direction to contingent labor, vendors, contractors in support of laboratory goals.

    • Previous experience effectively training new personnel required.

    • Knowledge of and effective use of Standard Operating Procedures (SOPs) is required.

    • Must be able to basically read, write, and speak English; ability to understand verbal and written instructions.

    • Must have good organizational skills, high degree of accuracy in testing and completing paperwork, and legible handwriting.

    • Demonstrated ability to adhere to safety and Personal Protective Equipment (PPE) is required.

    • Good interpretive judgment and skills to coordinate timing of testing and material flow by following production schedule is required.

    • Personal computer (PC) skills required, including skills in Microsoft Word, Excel and Laboratory Information Management systems (SAP-QM) and Empower HPLC.

    In addition, we will value: a Proactive, Curious, Result Focused person with Efficient Communication.

    We await your application


     

    Si consideras que reunís los requisitos para el puesto y te gustan los desafíos, no lo dudes…. ¡Envíanos tu CV!

     

     

    Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.

    ¡Esta propuesta te puede interesar!

    En Randstad nos moviliza ayudar a las personas y a las organizaciones a desarrollar todo su potencial. Ese es el compromiso que asumimos como compañía en todo el mundo, un compromiso que nos impulsa a ir más allá para lograr que nuestros clientes y candidatos alcancen el éxito. ¿Cómo lo hacemos?, combinando nuestra pasión por las personas con el poder de la tecnología, creando experiencias más humanas, que nos permitan ser una fuente de inspiración y apoyo para quienes nos eligen. Porque estamos convencidos de que mejores personas hacen mejores empresas.

     

    From our Healthcare & Life Science division, we are looking for an Important Multinational Pharmaceutical Company, for a Physical Chemical Analyst for product quality control, in the area of Pilar.

    Key Tasks & Responsibilities:

    • Adhere to all aspects of Corporate and Plant safety programs, GMP’s, ISO standards or other regulatory requirements.

    • Perform and support standard qualitative and quantitative analysis on in-process products, packaging components, bulk and finished products in accordance with the approved testing procedures.

    • Adhere to Regulatory guidelines for documentation, ensuring accurate, clear, legible and complete records of all information related to the sample login and release, analytical testing and investigations, preventive maintenance and instrument calibration, inventory and training.

    • Trained/qualified on basic and various analytical techniques, instruments and equipment, for qualitative and/or quantitative analysis.

    • Prepare laboratory reagent solutions for in process and finished products per monograph procedures as needed to support the laboratory. Prepare sample placebos for method development and validations.

    • Perform glassware washing to support the laboratory. Distribute and maintain adequate levels of clean glassware as required for testing needs. 

    • Prepare and file retain samples for bulk products. Maintain the sample file room. Manage the monthly retains for all tested samples.

    • Responsible for filing the laboratory documentation and the review of the laboratory documentation prior to filing.

    • Update the records for testing procedures and monographs when revised or replaced. Responsible for returning the obsolete monographs to QA.

    • Assist supervisor with revising SOPs, testing procedures and training material, with non-compliance investigations for in-process work and other special assignments as directed.

    • Participate in laboratory safety audits and solvent dumping schedule.

    • Participate in QC weekly PSS dialogue.

    • May perform other duties as assigned, including housekeeping tasks.

    Qualifications and Competencies: 

    • University degree (Chemical, Biotechnology, Physico-Chemical) or advanced degree in science/ engineering.

    • At least 3 years of GMP Lab experience required, showing demonstrated ability to accurately conduct routine QC tests in accordance with approved written procedures and demonstrated ability to follow production schedule with minimal direction from her/ his manager.

    • Demonstrated ability to give direction to contingent labor, vendors, contractors in support of laboratory goals.

    • Previous experience effectively training new personnel required.

    • Knowledge of and effective use of Standard Operating Procedures (SOPs) is required.

    • Must be able to basically read, write, and speak English; ability to understand verbal and written instructions.

    • Must have good organizational skills, high degree of accuracy in testing and completing paperwork, and legible handwriting.

    • Demonstrated ability to adhere to safety and Personal Protective Equipment (PPE) is required.

    • Good interpretive judgment and skills to coordinate timing of testing and material flow by following production schedule is required.

    • Personal computer (PC) skills required, including skills in Microsoft Word, Excel and Laboratory Information Management systems (SAP-QM) and Empower HPLC.

    In addition, we will value: a Proactive, Curious, Result Focused person with Efficient Communication.

    We await your application


     

    Si consideras que reunís los requisitos para el puesto y te gustan los desafíos, no lo dudes…. ¡Envíanos tu CV!

     

     

    Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.