Associate Scientist II

Grow with Cytiva - Innovate for Better Health

At Cytiva youll be part of a global life sciences company dedicated to advancing human health. Youll work alongside passionate colleagues to support customers driving breakthroughs - from cuttingedge research to vaccines medicines and cell and gene therapies. With a strong culture of learning collaboration and care for people and the environment Cytiva offers a place where you can grow your career while making a real impact on lives around the world.

What youll do

• Execute basic-complexity validation testing in accordance with lab requests SOPs and regulatory requirements ensuring accuracy and compliance.

• Prepare testing activities by reviewing lab requests and MSDS and ensuring all required materials and equipment are available and ready.

• Operate and troubleshoot laboratory instruments to ensure accurate and compliant test execution promptly communicate any deviations or issues to the Lab Manager (and Project Manager when necessary).
• Accurately record raw data and generate clear complete and reliable lab reports ensuring ontime delivery.
• Ensure test equipment and work areas are properly disassembled cleaned and maintained in compliance with 5S requirements.
• Handle filter performance complaint testing (POR Cases) as required and within defined timelines including integrity testing and destructive analysis conduct troubleshooting and collaborate with the global QE/QA team to support issue resolution when necessary.

• Take responsibility for assigned validation projects of basic complexity supporting project planning execution and delivery under guidance.
• Review interpret and prepare project protocols and reports in accordance with requirements and update related templates as needed.
• Work with internal and external customers to clarify project scope provide basic technical input and ensure testing plans meet regulatory and quality expectations.
• Maintain regular communication with customers and internal stakeholders providing project updates and addressing basic technical questions.
• Track project progress and report status and issues to management in a timely manner.
• Support internal projects related to R&D NPI/NPD and QC release testing as required.
• Other daily management work if necessary

Who you are

• Bachelors or Masters degree in Life Science Biology Chemistry or a related discipline.
• 1 - 2 years of experience in a biotech pharmaceutical or laboratory environment.
• Hands-on experience with basic laboratory techniques and measurement methods.
• Familiarity with GLP GMP and validation experience are a plus.
• Strong analytical skills with the ability to identify issues and propose solutions.
• Strong time management skills with the ability to prioritize tasks and meet deadlines.
• Excellent written and verbal communication skills proficiency in spoken English is a plus.
• Desire to work closely with a diverse team and team player.

Join our winning team today. Together well accelerate the real-life impact of tomorrows 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 .