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Bioprocess specialist

Visp
KPC International
Inserat online seit: Veröffentlicht vor 11 Std.
Beschreibung

KPC International - Excellence from Concept to Completion
KPC International began operations in 2001, our team of Engineers and Scientists have helped our clients achieve project success all over the world within the pharmaceutical and biopharmaceutical space.
We specialise in Plant Facility Start-Up from Strategy and Planning to Execution, through to Operational Readiness. We are proud to support our clients in delivering their life changing products to patients.
As a Bioprocessing Specialist your responsibilities will include:
Main duties
Bring energy, knowledge, and innovation to carry out the following:
Reporting to the Manufacturing Science & Technology Laboratory Lead, the responsibilities 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: 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.
Essential Skills/Qualifications:
To excel in this role, you will more than likely have:
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.
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.
KPC -International offers an inclusive environment where you can broaden your experience, perspective and skills to help make an impact on the lives of others.
KPC – International is an Equal Opportunity Employer.
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