Oct 26, Q-Sourcing Production Supervisor (Medical Devices Manufacturing) Jobs in Uganda

oct-26,-q-sourcing-production-supervisor-(medical-devices-manufacturing)-jobs-in-uganda

Q-Sourcing Production Supervisor (Medical Devices Manufacturing) Jobs in Uganda

Job Summary

The role of a Production Supervisor in a medical devices manufacturing facility is to supervise the manufacturing and production processes of medical devices.

Duties and Responsibilities

  • Analyzing production data and metrics to identify trends, issues, and opportunities for process improvements.
  • Set daily/weekly/monthly objectives and communicate them to employees
  • Organize workflow by assigning responsibilities and preparing schedules
  • Oversee and coach employees
  • Ensure the safe use of the equipment and schedule regular maintenance
  • Check production output according to specifications
  • Ensuring compliance with environmental, health, and safety regulations and guidelines.
  • Developing and implementing policies and procedures that improve production efficiency, quality, and safety.
  • Ensuring that manufacturing processes and equipment are maintained and repaired to minimize downtime and ensure high levels of productivity.
  • Enforce compliance with QA processes, Equipment Qualification, and Computer System Validation principles. Support all regulatory and customer quality audits.
  • Gather, organize & analyze data to develop solutions & alternative methods of proceeding; execute continuous improvement projects to optimize operations to deliver process improvements
  • Assist CAPA teams, and other project teams, in the development of action plans and implementation schedules, and the verification of completed actions.
  • Identify compliance issues that require follow-up or investigation.
  • Conduct or direct the internal investigation of compliance issues.
  • Conduct or direct the internal investigation of customer complaints.
  • Track compliance issues within all departments and ensure completion within defined timelines.
  • Assess product, compliance, or operational risks and develop risk management strategies.
  • Disseminate written policies and procedures related to compliance activities.
  • File appropriate compliance reports with regulatory agencies.
  • Evaluate testing procedures to meet the specifications of environmental monitoring programs.
  • Verify that software technology is in place to adequately provide oversight and monitoring in all required areas.
  • Maintain documentation of compliance activities, such as investigation outcomes.
  • Consult with corporate attorneys as necessary to address difficult legal compliance issues.
  • Discuss emerging compliance issues with management or employees.
  • Advise internal management or business partners on the implementation or operation of compliance programs.
  • Provide assistance to internal or external auditors in compliance reviews.
  • Prepare management reports regarding compliance operations and progress.
  • Monitor compliance systems to ensure their effectiveness. Oversee internal reporting systems such as corporate compliance hotlines and inform employees about these systems.
  • Develop or implement environmental compliance plans for programs, such as air, surface and personnel sampling.
  • Set daily/weekly/monthly objectives and communicate them to employees,
  • Organize workflow by assigning responsibilities and preparing schedules,
  • Oversee and coach employees, Ensure the safe use of equipment and schedule regular maintenance,
  • Check production output according to specifications, Train new employees on how to safely use machinery and follow procedures

    Qualifications & Experience

  • In science-related fields such as Pharmacy, Chemical/Mechanical/Biomedical Engineering, and Biotechnology.
  • 5+ years of production in BioPharma/biotech or similar technology-based industries such as cell and gene therapy.
  • Experience with SAP for production & manufacturing a plus
  • The applicant should have a High degree of integrity.
  • Ability to work as part of a team.
  • Ability to deliver accurate results in a timely manner and in an environment with multiple and challenging tasks.
  • Knowledge of Occupational Safety and Health Administration regulations
  • Strong verbal and written communication skills

    How to Apply

    For more information and job application details, see; Q-Sourcing Production Supervisor (Medical Devices Manufacturing) Jobs in Uganda

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