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Production Operator

  1. Ireland, Dublin
County Dublin
  1. Contract
Competitive
  1. CAPEX Projects
36065
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Production Operator - Pharma - Dublin - 11 months + possible extension 

This is a fantastic opportunity to be part of a fast-paced, €700 million project; with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.  

This is a truly exciting project, which when complete will contribute to the manufacturing of a life changing treatment.


Role Functions:
  • Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the Biotech facility manufacturing facility.
  • Support Equipment Design/ HAZOP and Room programming reviews as per requirements.
  • Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
  • Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
  • Work as part of a dedicated process team where flexibility and teamwork are a key requirement
  • Generate SOPS/Electronic Batch Records for start-up.
  • Adhere to Right First-Time principals
  • Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
  • Escalate issues as appropriate to Process Lead
  • 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.

Experience, Knowledge, Skills, and Qualifications:
  • Demonstrated successes in a team environment, such as project teams, Lean Six Sigma team, etc.
  • Demonstrated problem solving capabilities.
  • Knowledge of applying Lean Six Sigma and Lean methodologies in a workplace environment
  • Experience in a highly regulated pharmaceutical manufacturing environment is desirable.
  • Start-up experience in a large-scale commercial drug substance facility desirable but not essential.
  • Good understanding of Upstream/Downstream Processing and experience an advantage.
  • Ability to interact with multiple stakeholders across numerous departments
  • Excellent communication skills and the ability to work in a cross functional collaborative environment.
  • Good interpersonal skills, attentiveness, and an approachable manner for interactions with inter departmental colleagues.
  • Minimum of a Level 7 qualification in a science or engineering discipline.
  • A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.

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

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