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:
1. 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.
2. Support Equipment Design/ HAZOP and Room programming reviews as per requirements.
3. Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
4. Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
5. Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
6. Generate SOPS/Electronic Batch Records for start-up.
7. Adhere to Right First-Time principles.
8. Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
9. Escalate issues as appropriate to Process Lead.
10. 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.
11. 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:
1. Demonstrated successes in a team environment, such as project teams, Lean Six Sigma team, etc.
2. Demonstrated problem solving capabilities.
3. Knowledge of applying Lean Six Sigma and Lean methodologies in a workplace environment.
4. Experience in a highly regulated pharmaceutical manufacturing environment is desirable.
5. Start-up experience in a large-scale commercial drug substance facility desirable but not essential.
6. Good understanding of Upstream/Downstream Processing and experience an advantage.
7. Ability to interact with multiple stakeholders across numerous departments.
8. Excellent communication skills and the ability to work in a cross functional collaborative environment.
9. Good interpersonal skills, attentiveness, and an approachable manner for interactions with inter departmental colleagues.
10. Minimum of a Level 7 qualification in a science or engineering discipline.
11. 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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