Bio Process Associate
- Ireland, Dublin
- Contract
- CAPEX Projects
This vacancy has now expired
Would you like to grow your career, whilst contributing to scientific innovations that are transforming patients’ lives? Our client, a globally renowned biotechnology organisation, and voted one of the top 10 best companies to work for in Ireland, is looking to recruit a Bio Process Associate to join their team.
Responsibilities:
- Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps to facilitate the implementation of the project design and validation of the MPCC manufacturing facility.
- Creation of operating procedures & other relevant documentation for large scale manufacturing
- Execution of commercial manufacturing processes according to established work instructions.
- Adheres to Good Manufacturing Practices and Standard Operating Procedures.
- Takes part in investigations and optimisations of processes using scientific, engineering and lean principles
- Operates all production equipment within the assigned functional area
- Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.).
- Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative and provide input to related investigations and QA audit activities.
- Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment.
Requirements:
- 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)
- Ideally possess 1-3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility
- Experience with Delta V and MES would be considered an advantage.
- The successful candidate must demonstrate an ability to work independently and also as part of a team.
- The successful candidate must demonstrate problem solving ability and to adhere to scheduled timelines.
- Excellent communication skills and the ability to work in a cross functional collaborative environment are required.
If this role is of interest to you, please apply now!
#LI-JS4
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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