Production Operator
- Ireland, Dublin
- Contract
- CAPEX Projects
This vacancy has now expired
Do you want to be involved with exciting pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Production Operator.
This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.
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
Responsibilities:
- 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.
- 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.
If this role is of interest to you, please apply now!
#LI-AS3
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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