Specialist in Process Development v Praha – Holešovice,… - Jobeax
Popis nabídky
Specialist in Process Development v Praha – Holešovice, Česko
SOTIO a.s.
Plný úvazekStandardní týdenní pracovní doba
SmlouvaNa dobu určitou nebo freelance
Czech Republic
Specialist in Process Development v Praha – Holešovice, Česko is listed on Jobeax. Browse 80,000+ vacancies available.
At SCT Cell Manufacturing s.r.o., part of the PPF investment group, we strive to lead the way towards advancing the field of cell therapy and biologics manufacturing, with the goal of delivering benefits to patients.
⏩ We now have a unique career opportunity for you in the Process Development team⏪
What is our goal?
Our goal is to develop, optimize, and transfer robust manufacturing processes and analytical methods for cell and gene therapy products, supporting a wide range of client projects from development to GMP implementation.
What working in the Process Development team brings to you?
A hands-on scientific role combining laboratory work, data interpretation, and technical problem-solving
Experience across a diverse portfolio of cell and gene therapy projects within a multiproduct CDMO
Close cooperation with clients and cross-functional teams, including Manufacturing, QC, QA, PD/AD, and Project Management
The opportunity to develop your knowledge of GMP requirements, technology transfer, and technical documentation
Your Activities 🔬
Act as technical owner of process and analytical development, optimization, and technology transfer projects
Apply molecular biology, cell biology, and immunology knowledge in experimental design, data interpretation, and troubleshooting
Support process and analytical method characterization, validation activities, and GMP readiness
Cooperate on the transfer of processes into GMP manufacturing, including scale-up and implementation
Work closely with Manufacturing, QC, QA, PD/AD, Project Management, and other stakeholders
Support technical discussions with clients, data interpretation, and presentations
Support process investigations and troubleshooting related to product quality and process performance
Prepare and revise technical documentation, including SOPs, batch records, and development reports
Contribute to audits, CAPA, deviations, change control, and documentation for regulatory submissions
Support the technical evaluation of new opportunities and preparation of proposals
Qualification requirements
✅ A university degree or relevant practical experience in immunology, cell biology, molecular biology, biochemistry, or a related field
✅ Experience with process development, analytical development, or technology transfer is an advantage
✅ Previous experience in a GMP-regulated laboratory or manufacturing environment is beneficial but not essential
✅ A positive attitude towards documentation, strong attention to detail, and the ability to work effectively within clear rules and structured processes
✅ Good spoken and written English skills required for communication with international clients, participation in technical discussions, and preparation of technical documentation
Where is our office
Jankovcova 1518/2, 170 00 Prague 7
Are you ready to take on this challenge and become part of our Process Development team?
The selection process usually involves 2-3 rounds, during which we get to know each other and clarify our expectations.
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