Berlin Berlin Germany
Job Type: Regular Full-time
Division: Precision for Medicine
Business Unit: Translational Sciences
Requisition Number: 5912

QUALIFICATIONS

Minimum Requirements:

• PhD in biological sciences or equivalent, with current laboratory experience in IHC and mIF, ideally in a regulated laboratory (GLP/GCLP).
• Significant and current experience in generating, analysing and reporting high quality research data using automated IHC and mIF.
• Excellence in scientific writing for communication and reporting.
• Evidence of scientific project management experience preferred.
• High degree of computer literacy for research and reporting. Competent in MS Office and the use of databases

ADDITIONAL REQUIREMENTS:

• Previous experience working in a customer-oriented research (CRO) environment
• Proficient in basic computer applications such as MS Office, Word, Excel, PowerPoint and other relevant industry computerized systems, eg databases
• Proficiency in written and spoken English and German
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• Effectively design, develop, validate and execute automated IHC and mIF assays to support services projects, ensuring assays encompass relevant tissues, reagents and controls.
• Lead the implementation of molecular pathology assay and platforms to support current and new service lines.
• Provide high quality intellectual and practical expertise for services projects by designing, performing, analysing, interpreting and reporting experimental data, including the development of algorithms and spatial analyses following multiplex staining.
• Responsible for generating, protecting, and maintaining integrity (quality control) of raw, analyzed, reported data and associated metadata, including samples, reagents, methodology details and results.
• Keep organised, accurate and up-to-date paper and electronic scientific records and other operational records required.
• Actively seek new methodology and approaches, transferring new techniques to Precision
• Provide scientific support for commercial activities when required e.g. presentations and scientific discussions at face-to-face meetings with clients, supporting marketing materials.
• Act as Analytical Project Manager for GCLP regulatory studies, ensuring that all studies are performed in compliance with the principles of GCLP as required and maintain current knowledge of the regulatory requirements relevant to the role.
• Comply with quality management and regulatory requirements
• Effectively manage direct report(s) and across matrix when required.
• Train others in molecular pathology assays and assist team members in areas of own expertise
• Endeavour to continually improve working efficiency.
• Actively participate in performance review and personal development processes required.