Senior Validation Manager

hace 4 semanas


Alcobendas, Madrid, España Cytiva A tiempo completo
Job Summary

As a Senior Validation Manager at Cytiva, you will play a key role in leading paid service customer-specific technical projects. This position involves working directly with external biotech customers and internal commercial teams to define, implement, and complete customer-specific technical projects. Your primary responsibility will be to generate specific test protocols and reports to support customer requests and assigned responsibility for intermediate to complex projects.

Key Responsibilities
  1. Lead, delegate, review, and oversee projects of intermediate to complex complexity with minimal guidance and direction.
  2. Co-lead or lead technical consultations with customers (internal and external), involving validation testing plans and data review, test recommendations based on regulatory knowledge and expectations, and leveraging Subject Matter Experts (SMEs).
  3. Lead team collaboration and communication to ensure all test requirements are in place.
  4. Travel to customer sites for technical meetings and co-lead or lead customer trainings/presentations, utilizing SMEs.
  5. Establish project priorities and decide appropriate actions required to meet required target dates/schedule work into the laboratory in conjunction with the laboratory team leaders/ensure all projects meet or exceed on-time-delivery expectations by the team.
  6. Update management of the status of assigned projects, including completion, delays, or problems – lead development and implementation of countermeasures.
Requirements
  1. Bachelor's, Master's degree, or PhD in Science or Life Science.
  2. Long-standing years of working experience in the biotech industry.
  3. Background in Microbiology and Chemistry Validation testing with an understanding of Filter/Filtration concepts.
  4. Skilled in advanced laboratory techniques and measurement methods/ability to perform complex test work/application of Good Laboratory Practice (GLP) as appropriate and familiar with Good Manufacturing Practices (GMP) requirements.
  5. Fluent in English (reading and writing).
  6. Able to travel – 10% travel, overnight.
  7. Must have a valid driver's license with an acceptable driving record.
About Cytiva

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. We bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. At Cytiva, our vision is to advance future therapeutics from discovery to delivery.

This position is part of the BIS-PDVS and will be fully remote. We offer a comprehensive package of benefits, including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. This job is also eligible for bonus/incentive pay.


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