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Contact Info
Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Manufacturing Process Specialist


Reference:RK8883 Location: Cork
Qualification:DegreeExperience:3-4 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Manufacturing Coordinator

Manufacturing Process Specialist
RK8883
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.



Main duties and responsibilities:

• 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.

• Lead by example and strive to perform to high standards at all times.

• Responsible and accountable for assuring the safe accomplishment of job activities, following

good environmental practices and procedures.

• Carry out routine and non-routine tasks delegated by the Operations Manager according to

appropriate procedures, values, and standards.

• Lead, support and participate in commissioning and qualification activities both current and

future projects (and annual re-qualification activities).




Experience and Education:

  • A relevant third level qualification in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science or Engineering
  • Manufacturing experience within a GMP regulated environment.
  • Experience of the cell culture or purification processes, Project / New equipment installation experience
  • Process engineering, DCS (e.g. Delta V), SCADA and PLC systems



If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.