Associate Director / Bioprocess Lead in MS&T
- Ireland, Dublin
- Contract
- CAPEX Projects
Do you want to be involved with exciting pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Associate Director / Bioprocess Lead in MS&T.
Essential Duties and Responsibilities for this role include, but are not limited to, the following:
- 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.
- Ideally a Master’s in Biological Sciences/ Chemical Engineering/ Biological Engineering/Chemistry.
- Extensive 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.
- Excellent oral and written communication skills, with the ability to effectively articulate understanding of process science to drive decision making, impact assessments, design of studies in a multi-disciplinary team environment.
#LI-DH1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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Dawn
I manage this role.