Manager, Validation & Laboratory Operations (Filtration, Pharmaceutical, GLP)
Madrid
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.
The Manager, Validation and Laboratory Operations for Cytiva is responsible for leading paid service customer specific technical projects.
What you will do: Lead, delegate, and review projects of intermediate to complex complexity with no guidance and direction.Co-Lead or Lead Technical consultation with customers (internal and external), involving validation testing plans and data review, and test recommendations based on regulatory knowledge and expectations, leveraging SMEs.Lead team collaboration and communication with the lab team to ensure all test requirements are in place.Travel to customer sites for technical meetings and co-lead or lead customer trainings/presentations, using SMEs.Establish project priorities and decide appropriate action 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.Update management on the status of assigned projects, including completion, delays, or problems – lead development and implementation of countermeasures. Who you are: Bachelor's, Masters Degree, or PhD in Science or Life Science.Long standing years of working experience in the biotech industry.Background in Microbiology and Chemistry Validation testing with an understanding of Filter/Filtration concepts.Skilled in advanced laboratory techniques and measurement methods / Ability to perform complex test work / Application of GLP as appropriate and familiar with GMP requirements.Fluent in English (reading and writing).Ability to travel – 10% travel, overnight.Must have a valid driver's license with an acceptable driving record.
At Cytiva, we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement.
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