수평: Mid-Senior level
직업 종류: Full-time
작업 내용
Job description
• Responsible for the planning and coordination of the analytical experimental work (method
development, -validation, -transfer, titrations, certification of reference standards) to be done in
support of assigned projects.
• Manages multiple assigned projects and tasks, establishes priorities, in line with the projectcustomer requirements and agreed timelines.
• Informs supervisor about potential technical/scientific challenges and risks, prioritization or
resources conflicts.
• Review, interpretation and reporting of the obtained analytical data.
• Certificate of Analysis, report and protocol writing/approval
• Ensures that applicable guidelines, established operating procedures and safety regulations adhering
to company work standards are being followed.
Qualifications
Education & experience
• You hold a bachelor degree with at least 2 years of relevant experience in chromatographic (UHPLC,
HPLC and GC) method development- validation and relevant experience in Non chrom tests like
titrations.
• In-depth knowledge and experience in GMP regulations and working in a GMP environment.
• In-depth technical knowledge and technical proficiency of different (instrumental) analytical
techniques (like UHPLC – HPLC, GC, titrations), including data handling systems (i.e. Empower).
• Knowledge and experience in analytical report writing using electronic document management
systems
• Previous experience in working in a global and/or matrix organization and collaboration with
external partners (e.g. contract research organizations, academics) is a plus.
Competencies
• Self-Awareness & Adaptability
• Ensure high scientific quality standards for experiments and take on responsibility for these
experiments.
• Efficient, flexible and dynamic
• Customer focus and results and performance driven
• Sense of Urgency
• Excellent communication skills (verbally and written)
• Excellent English written proficiency
마감 시간: 31-12-2025
무료 후보 신청 클릭
작업 보고
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