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Supervisor De Manufactura

Supervisor De Manufactura

BaxterXico, Veracruz, México
Hace más de 30 días
Descripción del trabajo
  • Vantive : A New Company Built On Our Legacy
  • Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company.

    Vantive

    • will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve.
    • We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

      At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre.

      Each of us are driven to help improve patients' lives worldwide.

      Join us as we revolutionize kidney care and other vital organ support.Purpose of the position : Ensure that products comply with current regulations and quality standards through continuous improvement, by monitoring the production program in accordance with quality, safety and quantity standards for the use of materials, coordinating the group's effort to meet the needs of internal and external customers.

      Main activities, responsibilities and authorities : Activities

    • Cover with the production program.
    • Develop improvement projects in the area of healing materials.
    • Achieve efficiency levels.
    • Maximize the use of assigned resources.
    • Maintain a work team 100% trained in assigned operations.
    • Ensure compliance with the safety procedures of the activities and the personnel in charge, with international standards, ISO 14000, OSHAS 18000 and official Mexican standards on safety.
    • Ensure that risks and aspects of their areas of responsibility are identified, evaluated and controlled.
    • Review that the production and packaging of the medical device complies with the established specifications and requirements indicated in this standard.
    • Without prejudice to the obligations and responsibilities that correspond to the health manager, in accordance with the applicable legal provisions.

    • Supervise that the personnel involved in production use the necessary clothing and safety equipment, in accordance with the corresponding PNO production procedure.
    • Carry out all activities adhering to EHS guidelines, Comply with training requirements according to PNO PESMASEG052; as well as participate in internal programs that contribute to the detection of unsafe conditions and opportunities for improvement in terms of safety.
    • Implement continuous improvement within the assigned process.
    • Responsibilities

    • Promote a culture of compliance with standards and ethical business practices in the organization.
    • Drive the implementation of the ethics and compliance program and prevent, detect and correct violations of the law, Baxter policies and code of conduct.
    • Implement Baxter's code of conduct, policies and procedures, including, but not limited to, the Global Interactions Policy and Third Party Policy and support processes, ensuring employee induction and training.
    • Identify Baxter compliance and legal risks in the country / cluster.
    • Monitor compliance with the requirements of Local Health Regulation (NOM-241-SSA1), of countries to which the product is exported, international standards ISO 9001 / ISO 13485 in the current version and corporate requirements.
    • As well as comply with the risk management process when applicable.

    • Comply with the Quality Management System (PECCADN014) - Compliance with the BPD and the applicable SOPs.
    • Positions that report to you : Assistant.

      Janitor.

      Operators of the manufacturing areas (Home Choice, Extrusion, Sets, Twin Bag).

      Certifier.

      Scrap Assistant.

      Collaborator profile Scholarship : Industrial Engineer, Mechanical Engineer, Maintenance Engineer, Chemist, Q.F.B., Biochemist or similar.

      Knowledge : Knowledge of Local Health Regulation (NOM-241-SSA1) and international standards ISO 9001 / ISO 13485.

      Trend analysis.

      Note : This position can be occupied by Workers in a Vulnerable Condition or Situation (TCSV), specifically LGBT+, women and men heads of family and / or older adults.

      Experience : 3 to 5 years as a supervisor, manufacturing facilitator or in the area of process or quality engineering within the organization as a preference, or a person who meets the education and demonstrates the aforementioned knowledge under supervision of a maximum period of 6 months.

    • Reasonable Accommodations
    • Recruitment Fraud Notice
    • Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and / or financial information.

      To learn how you can protect yourself, review our Recruitment Fraud Notice.

      138946

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    Supervisor Manufactura • Xico, Veracruz, México