Process Engineer

Posted 3 Days Ago
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Shanghai, Shanghai Municipality, Shanghai, CHN
In-Office
Junior
Biotech
The Role
The Process Engineer will lead technical projects for Single Use Customized hardware, involving design, execution, and innovation in biopharmaceutical processes.
Summary Generated by Built In

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 Process Engineer for Cytiva is responsible for the Single Use Customized hardware project and consumables designing. Including single use mixing and storage system, single use bulk filling system and single use filtration system and so on.

Being the technical lead of a project team to 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 with specification, on time and within budget.

This position is part of the Customer Engineering located in Shanghai. 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
    - Analyse Customer User Requirements specifications.
    - Communication with customer about SUT consumables and finish drawing of SUT consumables for upstream & downstream applications,   including single use mixing bags/storage bags/filtration manifolds/final filling manifolds/transfer sets…
    - Define technical solutions including 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 cost .
    - Request, analyze and implement quotations for all main sub suppliers and include in technical proposal .
    - Present and discuss technical solution with customer .
     
  • Project Execution
    - 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
    - Assessing and resolving complex technical/process issues
    - Execution and coordination of Qualification/Verification activities at the various project stages (pre-FAT, FAT, SAT, IV/OV)
    - Creation of technical documents and co-operate with Documentation team to assemble final technical documentation package.
    - Drive and Participate in Continuous improvement processes
     
  • New Technology Innovation
    - Drive and Participate in Continuous Technology improvement processes

The essential requirements of the job include:

  • BSc/MSc 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
  • Adequate industry knowledge on biopharmaceutical processes, technologies, products and their applications and in-depth knowledge and experience on hardware used in pharmaceutical GMP factories.
  • 1-3 years of experience in the design and engineering of process equipment for bioreactor, filtration, separation and purification equipment (Single use technology, direct or tangential flow, filtration etc.) used in a upstream & downstream process.

It would be a plus if you also possess previous experience in:

  • It will be preferred having 1-3 years of concept, knowledge and experience in system
  • Hardware validation work in which confirm what the team have designed and
  • Manufactured for the customer.
  • Experience in qualification activities (FAT/SAT) for process equipment in the
  • Biopharmaceutical industry.

Join our winning team today. Together, we’ll 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.

For more information, visit www.danaher.com.

Skills Required

  • BSc/MSc or equivalent in Biochemical engineering, Process engineering, chemical engineering or equivalent
  • 1-3 years of experience in process equipment design and engineering for biopharmaceutical applications
  • Adequate industry knowledge on biopharmaceutical processes and technologies

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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