_The Production Supervisor is able to achieve and maintain the standards of safety, quality, productivity and efficiency in the defined time; comply with the production programs through the coordination of the activities of its personnel, through an effective administration and communication with the rest of the support departments, all within the compliance of our Quality System._
- **ESSENTIAL DUTIES AND RESPONSIBILITIES**_
- _Reporting to the Technical Director of Manufacturing, this role will support Centerpiece's growth and Centerpiece's operational excellence strategies through:_
- _Overseeing policies and procedures related to the manufacturing process and quality system, ensuring compliance on the production floor._
- _Ensuring the effectiveness of the execution of policies and procedures related to their work and subordinates that may affect product and service quality._
- _Develop, motivate and guide personnel in charge of meeting the objectives of the turnover, absenteeism and recognition plans._
- _Ensure that the manufacturing process is in control (using statistical process tools), maintaining continuous improvement programs for key operational indicators._
- _Coordinate the transfer of responsibilities and information between both shifts._
- _Responsible for the correct execution of line clearance procedures in their areas._
- _Maintain records of production, production line efficiency, loss time, documentation required by the process and DHR, etc._
- _Ensure the correct administration of the payroll of your personnel._
- _Comply with following safety policies and procedures._
- _Responsible for meeting EHS, Quality and Productivity objectives and integrated_ _support groups to work on tasks or projects necessary to organize improvement activities and achieve area objectives._
- _Promote training of own and subordinates._
- _Verify the applicable trainings of his personnel in charge, according to the activities executed._
- _Responsible for verifying the applicable curricula of their personnel in charge according to the activities carried out._
- _Comply with the regulations and policies on the C-TPAT program and the safety of the facilities._
- **QUALIFICATIONS**_
- Required Knowledge, Skills, and Experience:_
- _Bachelor's degree in engineering or related scientific discipline._
- _+5 years of progressively experience in a medical device industry or similar regulated industry._
- _English_
- _Office / BPCS/5's/GMP'S/ Six Sigma GB_
- _Ability to successfully manage multiple projects simultaneously._
- _Has professional presence with a level of comfort interacting with associates at all levels of an organization (internal and external), including executive management._
- _Fosters and actively contributes to a positive team working environment._
- Highly _motivated, self-starting person who takes pride in the quality outcome of their work._
- _Excellent interpersonal skills and a collaborative management style._
- _A demonstrated commitment to high professional ethical standards and a diverse workplace._
Tipo de puesto: Tiempo completo
Sueldo: $700.00 - $1,400.00 al día
Horario:
- Nocturno
- Rotativo
- Turno de 12 horas
Prestaciones:
- Estacionamiento de la empresa
- Opción a contrato indefinido
- Seguro de gastos médicos mayores
- Vales de despensa
Puede trasladarse/mudarse:
- 22740, Playas de Rosarito, B.C.: Trasladarse al trabajo sin problemas o planear mudarse antes de comenzar a trabajar (Obligatorio)
Experiência:
- Industria medica: 1 año (Obligatorio)
- GDP: 1 año (Obligatorio)
Idioma:
- Inglés (Obligatorio)
Lugar de trabajo: Empleo presencial
Fecha de inicio prevista: 29/04/2024
