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Location

Göttingen | Germany

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Job description

Analytical Scientist (all genders) - iPSC based Therapies page is loaded

Analytical Scientist (all genders) - iPSC based Therapies

Apply locations Goettingen time type Full time posted on Posted 4 Days Ago job requisition id REQ-06286

At Evotec’s site in Goettingen, Germany, the iPSC Cell Therapy department is seeking a highly motivated and dedicated

Analytical Scientist (all genders)

iPSC based Therapies

Full-time and permanent

We are seeking a dynamic and collaborative Analytical Scientist to play a pivotal role in advancing our state-of-the-art iPSC-based cell therapy products. The ideal candidate will be responsible for establishing and refining a diverse range of analytical methods. In this role, the selected candidate will be a key contributor to process development, process characterization, and product characterization. A deep understanding of method suitability for Quality Control implementation is essential for success in this position. The responsibilities include collaborating within a cross-functional team to ensure that the developed analytical methods can be seamlessly transitioned to GMP manufacturing and meet the highest quality standards.

Your key responsibilities:

• Independently design and develop complex molecular and cellular assays for characterization, in-process control (IPC), and release testing for cell therapy products
• Lead method qualification and optimization activities to ensure accuracy and reliability
• Independently and collaboratively design, execute, and troubleshoot experiments and proficiently analyze and present data
• Maintain meticulous records and author/review technical and regulatory documents for completeness, accuracy, consistency, and clarity
• Provide technical leadership and mentorship to less experienced team members.
• Drive method transfer and implementation into the Quality Control process
• Collaboratively drive projects to meet established timelines while upholding the highest quality and data integrity standards
• Assist in tech transfer activities and serve as a subject matter expert for matters relating to analytical methods
• Continually identify areas for improvement in project work and methods
• Contribute to the execution of development studies and routine laboratory operations and maintenance tasks

Your ideal qualifications:

• University degree in the biosciences, with several years of experience for candidates with a PhD, or at least 5 years of experience for candidates with a Master's degree, in analytical development within the pharmaceutical or biotechnology sector, particularly in the field of cell therapy
• Preferred familiarity with Good Manufacturing Practices (GMP) for biological products or Advanced Therapy Medicinal Products (ATMPs) or experience working in a regulated environment, e.g. GLP is a plus
• Strong expertise in several of the following methods: flow cytometry, dPCR/qPCR, ELISA, cell-based cytotoxicity/proliferation assays, and NGS. Expertise in method qualification/validation in a GMP environment would be highly desirable
• Experience in applying quality by design principles and Design of Experiments (DOE) approaches for analytical method development
• Working knowledge of statistical software tools, such as JMP or MODDE, is advantageous.
• Demonstrated ability to work independently to accomplish tasks
• High degree of initiative and flexibility, with the ability to work under challenging timelines
• Excellent communication skills with ability to interact professionally with all levels of staff, collaborators, and customers
• Fluency in written and spoken business English is necessary

Our offer:

• A position within a vigorous and exciting professional environment promoted by an open culture and a spirit of community
• A diverse, international workforce with a dynamic working environment that fosters creativity, innovations and teamwork
• 30 days of annual holiday, capital forming benefits, flexible working hours, holiday pay, annual variable bonus payment, and in-house canteen

To apply, please click on the “ Apply ” button and provide your application documents (CV, certificates and cover letter, including earliest possible start date and salary requirements). We are looking forward to get to know you and to your application.

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.

About Us

Evotec is a life science company with a unique business model that delivers on its mission to discover and develop highly effective therapeutics and make them available to the patients. The Company’s multimodality platform comprises a unique combination of innovative technologies, data and science for the discovery, development, and production of first-in-class and best-in-class pharmaceutical products. Evotec leverages this “Data-driven R&D Autobahn to Cures” for proprietary projects and within a network of partners including all Top 20 Pharma and over 800 biotechnology companies, academic institutions, as well as other healthcare stakeholders. Evotec has strategic activities in a broad range of currently underserved therapeutic areas, including e.g. neurology, oncology, as well as metabolic and infectious diseases. Within these areas of expertise, Evotec aims to create the world-leading co-owned pipeline for innovative therapeutics and has to-date established a portfolio of more than 200 proprietary and co-owned R&D projects from early discovery to clinical development. Evotec operates globally with more than 5,000 highly qualified people. The Company’s 17 sites offer highly synergistic technologies and services and operate as complementary clusters of excellence. For additional information please go to and follow us on X/Twitter @Evotec and LinkedIn .

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