BioProcess Associate
- Ireland, Dublin
- Contract
- Life Sciences
One of the top 10 best companies to work in Ireland is looking for BioProcess Associate for their large-scale new facility in Dublin. Is this you?
An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.
Responsibilities include:
- Execution of commercial manufacturing processes according to established work instructions
- Creation of operating procedures & other relevant documentation for large scale manufacturing
- Operating production equipment within the assigned functional area
- Adhering to Good Manufacturing Practices and Standard Operating Procedures
- Taking part in investigations and optimisation of processes using scientific, engineering and lean principles
- Proficient use of process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.)
- Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activities
- Working with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation and operation of the MPCC manufacturing facility
- Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and a safe working environment
- The successful candidate will ideally possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred)
- Working experience in a large-scale biopharmaceutical manufacturing facility would be a distinct advantage
- Experience with Delta V and MES or similar control and data acquisition systems would be desirable
- The candidate must demonstrate an ability to work independently and also as part of a team.
- A successful candidate will have a demonstrated problem-solving ability and the ability to adhere to scheduled timelines
- Excellent communication skills and the ability to work in a cross-functional, collaborative and fast-paced environment are essential
If this role is of interest, please apply now!
#LI-JS4
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
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
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