Non-Sterile Operator – Cleaning & Equipment Preparation

Zoetis Spain SL

Tallaght

On-site

EUR 32,000 - 42,000

Full time

14 days+
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Job summary

Zoetis in Ireland is seeking a Production Operator to perform cleaning and sterilization tasks in line with the production schedule, helping meet targets for OEE, quality, and health and safety standards.

You will manage line changeovers, material handling, documentation and handovers between shifts, supporting continuous improvement and adherence to cGMP throughout manufacturing operations on site in Tallaght.

Qualifications

  • Experience in a pharmaceutical environment is desirable.
  • Knowledge and understanding of cGMP principles and manufacturing desirable.
  • Lean manufacturing experience desirable.

Responsibilities

  • Primary responsibility for providing cleaning and sterilization services as per production schedule while ensuring they meet all relevant targets including line OEE, Quality, right first time, adherence to schedule, health & safety. (20%)
  • Responsible for Booking in, storage and distribution of the cleanroom garb and maintenance of consumables stocks in all areas, e.g. cleanroom supplies. (20%)
  • Providing cover for manufacture, sampling and dispensing of batches. Supporting the formulation, filling and packing process. (25%)
  • Effectively resolve or upscale problems in the manufacturing area to ensure problem solving can occur when and where issues happen. (5%)
  • Completion of all relevant documentation, batch EBR (electronic batch record) and training records. (5%)
  • Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and contribute to continuous improvement projects. (5%)
  • Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and lead / contribute to continuous improvement projects. (5%)
  • Work effectively with their colleagues through timely and relevant communication to ensure the shift meets its production goals and that a smooth handover exists between shifts. (5%)
  • Assist in 5S activities and help sustain the required 5s standards within their area. (5%)
  • Organize, prepare for, and participate in Line Changeovers in order to maximize the OEE potential. (5%)

Skills

Pharmaceutical environment experience
cGMP knowledge
Lean manufacturing experience

Job description

POSITION RESPONSIBILITIES
  • Primary responsibility for providing cleaning and sterilization services as per production schedule while ensuring they meet all relevant targets including line OEE, Quality, right first time, adherence to schedule, health & safety. (20%)
  • Responsible for Booking in, storage and distribution of the cleanroom garb and maintenance of consumables stocks in all areas, e.g. cleanroom supplies. (20%)
  • Providing cover for manufacture, sampling and dispensing of batches. Supporting the formulation, filling and packing process. (25%)
  • Effectively resolve or upscale problems in the manufacturing area to ensure problem solving can occur when and where issues happen. (5%)
  • Completion of all relevant documentation, batch EBR (electronic batch record) and training records. (5%)
  • Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and contribute to continuous improvement projects. (5%)
  • Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and lead / contribute to continuous improvement projects. (5%)
  • Work effectively with their colleagues through timely and relevant communication to ensure the shift meets its production goals and that a smooth handover exists between shifts. (5%)
  • Assist in 5S activities and help sustain the required 5s standards within their area. (5%)
  • Organize, prepare for, and participate in Line Changeovers in order to maximize the OEE potential. (5%)
ORGANIZATIONAL RELATIONSHIPS
  • Production Lead
  • Production Operator
  • Warehouse Personnel
  • Quality Personnel
EDUCATION AND EXPERIENCE
  • Experience in a pharmaceutical environment desirable.
  • Knowledge and understanding of cGMP principles and manufacturing desirable.
  • Lean manufacturing experience desirable.
PHYSICAL POSITION REQUIREMENTS

Note the physical conditions in which work will be performed, if applicable to the position. Examples: Lifting, sitting, standing, walking, ability to travel, drive, unusual attendance requirements, weekend work or travel requirements, etc. Lifting, sitting, standing, shift-hours. Full time Regular Colleague

Why Zoetis

Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers.

Zoetis work environment

At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow.

Your opportunities at Zoetis

We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health.

Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses.

Results that matter

Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face.

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