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MS&T Associate Director
| Reference: | RK23012 | Location: |
Dublin |
| Qualification: | Degree | Experience: | 7-9 Years |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
MS&T Associate Director
RK23012
Contract – 11 months
Dublin
Hybrid
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.
This role supports the development of the site, providing leadership and Drug Substance technical support, in the Process Sciences Laboratory. Leads/participates in cross functional teams to deliver all project and investigational activities on schedule. The successful candidate will develop a talented team of Manufacturing Science & Technology Scientists in delivery of new products for commercial operations.
Duties:
• Manage, coach, and mentor the MS&T drug substance team in performing advanced technical experiments. Inspire, reward and develop individuals, helping them to reach their potential.
• Technical Lead for MS&T Process Sciences and the site.
• To provide proactive, technical oversight of the biologics inline & pipeline products.
• Lead technical assessments for process investigations, risk assessments, evaluation of specifications and material qualification.
• Coach the team on development and execution of technical studies, continuous improvement of existing biologics processes and for new product launch.
• Complete experimental design, execution, data analysis and interpretation for improvement programs.
• Oversight of the product robustness trends observed in commercial operations and alignment with laboratory models, such as SIMCA for multivariate data analyses.
• Lead and/or support deployment and use of various digital tools at Biotech Dublin facility: Leverage these tools to deliver business value through predictive/proactive issue resolution, rapid investigation closure, improved yield/throughput.
• Assist in the regulatory authoring and review of technical documentation, technical report writing and global regulatory submissions.
• Support creation of the laboratory budget and review actual performance against forecast.
Educational and Experience:
• Ideally a Master’s in Biological Sciences/ Chemical Engineering/ Biological Engineering/Chemistry.
• 8+ years directly related working knowledge in academia, pharmaceutical or biotechnology company – along with a working familiarity of current regulatory requirements and current Good Manufacturing Practices.
• The successful candidate will also have demonstrated the ability to deliver projects and programs, with a strong understanding of lean and laboratory operations.
If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.
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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