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Senior R&D Manager/Director
Dublin
Dublin
Embedded Software Engineer
Dublin
Dublin
Manufacturing Engineer
Wexford
Wexford
Biomedical Engineer
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Dublin
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Galway
Galway
R&D Director
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Technical Transfer Specialist - Remote
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Carlow
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Galway
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Dublin
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Carlow
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Galway
Senior R&D Engineer
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Dublin
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Tipperary
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Galway
Galway
Head of R&D
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Galway
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Carlow
Carlow
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Galway
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Athlone
Athlone
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Galway
Project Manager
Louth
Louth
Quality Manager
Dublin
Dublin
Senior QC Associate
Dublin
Dublin
Analytical Chemist
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Tipperary
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Republic of Ireland
Republic of Ireland
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Athlone
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Limerick
Quality Systems Manager
Dublin
Dublin
Validation Engineer
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Limerick
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Carlow
Carlow
Senior Regulatory Affairs Specialist
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Westmeath
Process Support Specialist
Carlow
Carlow
Senior Operations Manager
Tipperary
Tipperary
Aseptic Process Owner Lead
Dublin
Dublin
Senior Recruitment Consultant
Republic of Ireland
Republic of Ireland
Senior R&D Project Manager
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Galway
Electronic Design Engineer
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Galway
Biomedical Engineer
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Senior Mechanical Engineer
Dublin
Dublin
Senior Quality Engineer
Dublin
Dublin
Principal Process Equipment Engineer
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Dublin South
EHS Systems Specialist
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Dublin
Specialist Operations Engineer
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Tipperary
QA Specialist
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Dublin
Dublin
R&D Senior Program Manager
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Galway
QC Chemistry Analyst (Shift)
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Qualified Person
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Clean Utilities Engineer
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Maintenance Engineer
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Facilities Engineer
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Principal R&D Engineer
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Maintenance Engineer
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Quality Validation Engineer
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Maintenance Reliability Engineer
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Tipperary
Project Engineer
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Republic of Ireland
Senior Associate Quality Control
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Dublin South
R&D Manager
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Sourcing Specialist
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Tipperary
Technical Transfer Specialist - Remote
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Republic of Ireland
Senior QC 24/7 Shift
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Dublin
Manufacturing Engineer
Galway
Galway
Senior Quality Engineer
Galway
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Senior Quality Engineer
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R&D Director
Galway
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Planner/Scheduler
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Lead Maintenance Reliability Engineer
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Senior R&D Engineer
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EHS Systems Specialist
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Chemical Engineer
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Republic of Ireland
Republic of Ireland
Microbiology Manager
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Quality Systems Specialist
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Senior Regulatory Affairs
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R&D Manager
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Senior R&D Engineer
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Carlow
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Tipperary
Apply for this job
Details
Manufacturing Specialist
Reference: | RK3143 | Location: |
Dublin |
Qualification: | Degree | Experience: | 4-5 Years |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Manufacturing Coordinator
Manufacturing Specialist
RK3143
12 Months
Dublin
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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.
Duties:
- Perform as a knowledgeable subject matter expert (SME), and single point of contact on site and network projects and programs, to advance manufacturing and aseptic operations through ownership of the assigned processes and taking a proactive approach to safety, quality, and compliance by actively seeking opportunities to remove error traps.
- Accountable for process documentation (e.g., SOPs, Training, Electronic Batch Records, Risk Assessments) in assigned area of responsibility. Gatekeeper (develop, review and update) of process documentation to maintain structure and control over generation and revision ensuring the documents clearly and correctly direct the process.
- Leading and/or providing input to strategic initiatives that will improve and develop processes for the future.
- Contribute in a team environment to operational issues pertaining to processes as they arise and provide expertise and support to help resolve escalated technical issues as required.
- Use subject matter expertise to identify and lead continuous improvement projects in assigned area of responsibility. Ensure project timelines are met, challenges identified, mitigations are in place and communication plans delivered to all stakeholders.
- Involved in the daily business management systems and reporting, have a clear understanding of what is happening in the assigned area of responsibility. Monitor any process trends including business performance metrics. Identify actions that will enable the process and the Manufacturing areas better achieve and surpass metrics in the future.
- Lead and/or Support investigations that impact on safety, quality and/or compliance of the processes, ensuring thorough investigations are conducted and actionable CAPAs, to prevent future reoccurrence, are implemented within agreed timeline.
- Remain current on state-of-the-art for systems and processes and advise on the appropriate adoption and use of new techniques and technology.
Education and Experience :
- Bachelor’s degree in Science, Engineering or related discipline with 5 + years’ experience in aseptic Drug Product Manufacturing or related cGxP manufacturing experience.
- Experience with regulatory compliance in cGMP manufacturing and in-depth knowledge of Eudralex Volume 4, Annex 1 Manufacture of Sterile Medicinal Products.
- Interacts well with diverse groups (Manufacturing, Validation, Engineering, Quality etc) and maintains strong working relationships with internal and external collaborators.
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.
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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
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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
Valid XHTML - CSS