Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
In this role, you will have the opportunity to:
Pre order Activities (Time Spent 20 %)
Analyze Customer User Requirements specifications
Define technical solutions including analysis of process mass balance, equipment selection and sizing, drafting process and instrumentation diagrams.
Write technical proposals including clarification and exclusion lists.
Create Project Costing sheets including material and manpower costs
Project Execution (Time Spent 70 %)
Develop Project Quality Plan & SAP project creation and maintenance.
Complete basic design including process and instrumentation diagram as per ASME BPE, component lists and process functional specifications
Cross functional communication, progress monitoring, co-ordination of sub-supplier activities (e. g. mechanical fabricators, electrical fabricators and software companies).
Execution and coordination of Qualification/Verification activities at the various project stages (pre-FAT, FAT, SAT, IV/OV)
General Administration & Specialized Activities (Time Spent 10 %)
Specialized responsibilities such as SAP key user, design authority and technical key account manager can be assigned to individuals based on their capabilities talents and interests.
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The essential requirements of the job include:
Minimum Qualifications:
BSc/MSc Biotechnology or equivalent in Biochemical engineering, Process engineering, chemical engineering or equivalent. A higher degree or secondary degree in a related subject would be an advantage
Experience of process engineering / project management of equipment used in Biopharmaceutical manufacturing
It would be a plus if you also possess previous experience in:
To work safely and to comply with the company’s health, safety and environmental (HSE) policies and procedures.
Position Competencies:
• Ability and willingness to work in a multinational and interdisciplinary team with a high degree of travelling.
• Ability to communicate effectively on complex technical / engineering issues at the highest level. Cytiva internal as well as with the customer.
• Knowledge and understanding of the current industry guidelines for designing, manufacturing, testing and documenting biopharmaceutical process equipment. (ASME BPE, GAMP, cGMP, ISPE, etc.)
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.