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Cytiva

Senior Product Engineer, Strategic Projects, Cytiva Filtration

Posted Yesterday
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In-Office
2 Locations
Senior level
In-Office
2 Locations
Senior level
Lead product engineering initiatives globally to enhance customer satisfaction and improve business growth in filtration technologies. Train teams and implement lifecycle processes while ensuring compliance and quality standards are met.
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Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry 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.

Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

What you’ll do:

The senior product engineer, strategic projects is executing initiatives globally with deep impact on customer satisfaction and business growth across a technological broad range of consumable products, including filtration membrane, hollow fibers, sterile connectors, filtration devices, single use systems and hardware. Main responsibilities of the senior product engineer are:

  • Drives the product engineering team and wider filtration quality and operations teams to execute processes in the best way ensuring customer expectations are met, this includes but not limited to:
    • Support the implementation of Filtration Product Lifecycle Process in Cytiva global system
    • Develop standard documentation practices aligned across all filtration manufacturing sites within process owned by product engineering
    • Support engineering team with the implementation of standard process, procedures and documentation to ensure product claims, specifications and their evidence are maintained and align with regulatory and customer’s requirements
  • Lead filtration product engineering teams training on global Filtration process and documentation.
  • To look for and implement opportunities for continuous improvement of processes to reduce cost and improve efficiency.
  • Support Customers Regulatory Support and Quality Assurance teams with customers communication as part of change control (data sharing, questions).

Who you are:

  • Master’s degree or equivalent in Biotech, Engineering or Chemistry or related discipline.
  • At least 5 years in Biotech industry (project management, process validations, product engineering, technical support or validation services).
  • Know the Biopharmaceutical manufacturing process, related technology (filtration devices, single-use technologies) and product validations (risk assessment, validation master plan) and qualifications (IQ, OQ, PQ).
  • Experienced with working in a matrix environment and managing several projects with dynamic timelines to execution (ability to prioritize, manage and execute multiple projects simultaneously, strong organizational skills, focused and results oriented).
  • Excellent interpersonal and communications skills (training skills, communication in front of a large audience globally, lead cross functional teams globally, interacting with scientific and technical personnel, including operations personnel, engineers and end users).
  • Apply critical thinking to challenge old ways and find new efficient solutions, to solve problems and to manage conflicts.
  • Fully proficient in English (writing and speaking).

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

  • Customers facing role such as Marketing, product management, technical support, sales specialist or technical inside sales.
  • Understanding cGMPs and pharmaceutical regulatory requirements.
  • Documentation management systems or tools implementation.

TRAVEL:

Punctual travel as needed up to 40%, including domestic and international travel to factories, centers of excellence and customers punctually. 

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.

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.

Top Skills

Biotech
Chemistry
Documentation Management Systems
Engineering
Filtration Devices
Single-Use Technologies

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