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Manufacturing Biotech Associate

  1. Ireland, Dublin
Dublin
  1. Contract
Competitive
  1. Life Sciences
32976

This vacancy has now expired

Manufacturing Biotech Associate - Pharmaceuticals - Dublin - 11-Months+

Do you want to be part of one of the top 10 best companies to work for in Ireland? We have a superb opportunity for Manufacturing Biotech Associate to join our client, a global pharmaceutical organisation in their new multifunctional facility. This is a truly exciting, €400 million project that will contribute to the manufacturing of life changing treatment, offering an abundance of opportunities to work with and learn about cutting-edge technologies.


Responsibilities: 
  • Provide immediate feedback to others at any time to reinforce good safety and improvement behaviours and acts.
  • Execute commercial manufacturing processes according to established work instructions and
  • Standard Operating Procedures (SOPs).
  • Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
  • Routinely talk about any safety issues you are concerned about.
  • Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
  • Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
  • Adhere to Right First-Time principles.
  • Provide assistance and/or support maintenance, engineering, quality, or other colleagues as requested.
  • Escalate issues as appropriate to manager/designer.
  • Maintain a high level of personal expertise and working knowledge of all aspects of the
  • manufacturing process and process equipment through continuous training and development.
  • Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan and site schedule.
  • Challenge and identify improvements to the safety and environmental programmes on site.
  • Celebrate with use of proactive recognition tools that inspire teams and individuals you collaborate with.

Requirements: 
  • Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 1 - 3 years’ experience in a GMP Manufacturing environment.
  • The minimum education/ experience (3 years) plus:
  • Experience of Upstream/ Downstream Processing.
  • Experience in a highly regulated pharmaceutical manufacturing environment.
  • This role will involve working shifts, on a 24/7 basis.
  • Excellent communication skills and the ability to work in a cross functional collaborative environment.

If this role is of interest to you, please apply now! 

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