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At European Recruitment, our sectors cover a wide range of industries within the field of technology
At European Recruitment, our sectors cover a wide
range of industries within the field of technology
At European Recruitment, our sectors cover a wide
range of industries within the field of technology
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At European Recruitment, our sectors cover a wide range of industries within the field of technology
MSAT Engineer (Process Chemist)
Recruitment Consultant
Adam Chapman
Contact Details
Posted
1 month ago
Responsibilities
Process Optimization and Monitoring:
- Perform laboratory scale experiments to support manufacturing non-conformances and lead continuous improvement projects (CIPs) including impurity purging capability, yield improvement, cycle time reduction and particle size distribution (PSD) optimisation.
- Serve as the Subject Matter Expert (SME) for Process Analytical Technology (PAT) initiatives, including plant-based MID-IR and Lasentec (FBRM) technology for monitoring critical parameters.
- Mobilize cross-functional teams to deploy live Multivariate Analysis (MVA) models, facilitating continuous process improvement.
Investigations and Innovation:
- Act as the Technical Process SME for Manufacturing Operations, providing expertise on investigations related to impurity deviations, low yields, emulsions, and PSD issues, while ensuring compliance with cGMP standards.
- Collaborate with internal and external stakeholders, including Regulatory Owners and Technical Owners, to support investigations, change controls, and CAPA development.
- Lead complex investigations with cross-functional teams, applying analytical and problem-solving skills to determine root causes, assess impacts, and implement process improvements.
Requirements
- PhD in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field.
- Minimum of 3 years of experience in a similar role within the pharmaceutical industry or equivalent.
- Experience in PAT techniques, MVA, and process optimization methodologies preferred.
- Strong understanding of cGMP regulations and experience in supporting investigations and regulatory audits.
- Excellent communication and collaboration skills, with the ability to lead cross-functional teams and drive process improvement initiatives.
- Demonstrated leadership abilities, including experience in project management and team coordination.
Industry
Life Sciences
Contract Type
Contract
Location
Ireland
Work Model
On-Site
Apply Now
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