Sr Production Supervisor

Achieve given team performance goals for Production. The goals will include efficiency, DPU, hour’s accuracy, scrap; time lost accuracy, DHR accuracy, as well as inventory metrics.

Roles & Responsibilities :

  • Hire, train, develop, and motivate production personnel to follow procedures, meet high quality standards, production schedules, and productivity requirements
  • Update and revise Manufacturing Process Instructions to ensure that MPIs are accurate and complete
  • Address line support issues as they arise (including technical-related issues)
  • Work closely with Engineering to resolve production issues and actively participant in quality improvement initiatives.
  • Document and report any variances, problems, issues, or concerns
  • Provide production personnel with expectations and performance feedback quarterly
  • Write and conduct formal annual performance reviews for production personnel
  • Plan, supervise, drive improvement, and report production performance including output, yields, root cause failures, efficiencies, and trends
  • Understand, train personnel, and enforce strict adherence to the applicable DOPs and SOPs of the Quality System, as well as the Manufacturing Guidelines
  • Assist in setting and attaining quarterly and annual production goals
  • Learn and enforce company safety policies and practices
  • Lead or support various Lean Manufacturing initiatives that involve a Mfg. based team.
  • Support sub-assembly or process outsourcing initiatives
  • Generate / Review / approve ECOs to determine impact on manufacturing.
  • Review and disposition discrepant material. Implement corrective actions to prevent recurrences.
  • Evaluate designs for manufacturability (with respect to tooling and assembly methods). Provide suggested change proposals, or tooling concepts during early design process phase.
  • Drive our Culture Strategy by fostering our mission, founding principles, individual and leadership expectations.
  • Work closely with corporate engineering on production line transfer or improvements.
  • Support corporate Quality improvement CAPA implementations
  • Assist engineering with Final Manufacturing Review.
  • Assist budget spending to preprocess and execution.
  • Education and / or Experience : Bachelor's degree on related fields.
  • Five years of either supervisor and / or engineering experience. Experience in the medical device industry is preferred, specifically in high-volume manufacturing area.
  • Strong working knowledge of Lean Manufacturing, DFT, and 6 Sigma (GB / BB - highly recommended).
  • Proficient in the use of personal computers to perform daily work. Familiar with the Microsoft Office suite of programs and MRP systems.
  • SAP and Agile experience preferred.

  • Superb communication skills, including written and verbal instruction.
  • The ideal candidate will have a love for a fast-paced and multi-focused work environment.
  • Bilingual English / Spanish
  • Shift : Shift 2 - Evening

    Travel : Yes, 10 % of the Time

    Travel Requirements : Yes, 10 % of the Time Shift : Shift 2 - Evening

    Publicada el 04/06/2021

    Finaliza el 04/07/2021

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