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Apply for this job
Details
Upstream Manufacturing Process Specialist (hybrid)
Reference: | AS0083 | Location: |
Cork |
Qualification: | Degree | Experience: | 4-5 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Biomedical Engineer, Bioprocess Engineer, EHS Specialist, Engineering Manager, Maintenance Engineer, Pharmaceutical Engineer, Process Engineer
Upstream Manufacturing Process Specialist (hybrid)
AS0083
Contract – 12 months
Cork
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
This position is responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within Operations.
Duties:
- Represent Operations on cross functional project implementation teams.
- Monitoring and troubleshooting of the manufacturing process and equipment issues and process optimization.
- Monitoring and reporting of process performance using statistical process control.
- Troubleshooting of DCS (e.g Delta V) and PLC control systems.
- Investigating and resolving issues raised within the Manufacturing Department.
- Participate in/ Lead Cross Functional teams when required.
- Support of Commissioning and Qualification activities.
- Preparation and updating of Batch Records, Procedures and Work Instructions.
- Provide process and equipment related training as required within the Manufacturing Department.
- Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements.
- Bachelors Degree in a scientific/technical discipline required.
- A minimum of 5 years’ experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
- Industry experience in upstream fed batch bioreactors.
- Experience of DCS (e.g. Delta V), SCADA and PLC systems.
- Manufacturing experience within a GMP regulated environment.
- Experience of the cell culture or purification processes and Project / New equipment installation experience.
If interested in this posting please feel free to contact Avishek Singh on +353 (0)87 282 7991 [email protected] further information.
Engineering Chemistry Biotechnology Dublin Packaging Engineer Project Manager Quality Assurance Allied Healthcare Medical Device Scientist Supply Chain Supply Chain Life Science Microbiology Manufacturing Executive Clinical Research Academic Limerick PhD Connected Health Cork City Diagnostics Academic Medical Affairs Cork Quality Engineering Scientific Mayo Sales and Marketing Biopharmaceutical Laboratory Scientist IT Sales and Marketing Pharmaceutical Quality Control Pharma Sales Validation Engineer Product Development Engineer
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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