Senior Process Engineer

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. The Senior Process Engineer for Cytiva is responsible for: •   Analyze customer process user requirements specification for Cytiva equipment used in the Biopharmaceutical industry, which will focus on downstream system. •   As technical lead of a project team discusses, propose, define final technical system solution with the customer including writing technical part of quotation and associated costing. After Order placement execute the proposed engineered system solution based on agreed and defined contractual specification together with a defined project team as project manager or process engineer. •   Make sure the projects are delivered in accordance to specification, on time and within budget. •  Take ownership of very complex technical tasks and issues. •   Manage and co-ordinate small to large-size projects •   It will be preferred that the candidate has systems engineering competence within the automation & electrical area and can advise vendors & customers on automation potential in manufacturing and assembly systems. •    It will be also preferred that the candidate support validation tests in accordance with test requests, specifications, have good knowledge of system manufacturer’s specifications and GMP validation standard for biotech devices.   This position is part of the Custom Engineering, BioProcess China, located in Shanghai, China and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. In this role, you will have the opportunity to: Pre order Activities (Time Spent 30 %) •   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 •   Request, analyze and implement quotations for all main sub suppliers and include in technical proposal •    Develop Project schedules •    Perform Project Risk assessments •    Present and discuss technical solution with customer Project Execution (Time Spent 60 %) •    Contract review following customer order •    Magic project creation and maintenance •    Develop Project Quality Plan •    Complete basic design including process and instrumentation diagram, component lists and process functional specifications •    Obtain valid quotations for all materials and initiate orders with procurement. •    Cross functional communication, progress monitoring, co-ordination of sub supplier activities (e. g. mechanical fabricators, electrical fabricators and software companies). •    Progress monitoring, reporting and control •    Financial status monitoring, reporting and control •    Coordination of incoming goods inspection •    Assessing and resolving complex technical/process issues •    Coordination of Qualification/Verification activities at the various