Production Supervisor
Philips
Alajuela
hace 4 días

Job Description

In this role, you have the opportunity to

Supervises the implementation of activities in production area(s) to meet production goals, quality, and cost objectives.

Plans and administers procedures within the assigned production department. Develops schedules and manpower requirements for assigned areas.

Selects, develops, and evaluates personnel to ensure the efficient operation.

Administrative :

  • Ensure all procedures utilized in manufacturing are current and up to date
  • Track employee attendance records on a daily basis
  • Train employees in new documents as required
  • Communicate vital information and company communications
  • Write and deliver employee performance reviews
  • Logistical Responsibilities;
  • Ensure all procedures utilized in manufacturing are current and up to date
  • Track employee attendance records on a daily basis
  • Communicate vital information and company communications
  • Write and deliver employee performance reviews
  • GMP / Safety / Documentation;
  • Communicate effectively with management and other support teams
  • Ensure GMP guidelines are followed at all times
  • Communicates process improvement suggestions to engineering and management
  • Ensure a safe work environment is maintained at all times
  • General Duties;
  • Makes recommendations regarding staffing
  • Writes production reports based on yields, issues, process controls
  • Properly balances staffing per production area
  • Manages WIP inventories
  • You are a part of

    A leading health technology company with a multinational workforce of approximately 77,000 employees and globally present with sales and services in more than 100 countries worldwide.

    To succeed in this role, you should have the following skills and experience

    EDUCATION :

  • Requires a bachelor’s degree in related field or equivalent training.
  • Adequate combination of educational background and / or experience in Medical or electronic Companies to effectively perform self-training.
  • KNOWLEDGE AND EXPERIENCE DESIRABLE :

  • 2+ years’ experience in manufacturing process; preferred but not limited to medical device industry or electronic industries.
  • Proven experience in leading others with a proactive attitude.
  • Strong manufacturing background with evidence of process evaluation knowledge is a plus.
  • Desirable working knowledgeable of FDA regulations, Quality System Regulations (QSR), ISO 13485 and Japan regulations are a plus.
  • In return, we offer you

    In order to develop your full potential, we will offer you the flexibility, encouragement and opportunities to keep you inspired and engaged.

    After all, working at Philips is more than a job. It is an experience full of amazing moments that will transform you in a lasting and positive way, since together we can improve the world.

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