Posted:8 hours ago|
Platform:
On-site
Full Time
We are seeking a highly organized and detail-oriented individual to manage and audit sample-related information within our LIMS system. This role involves critical data review, direct client communication, and collaboration with various internal teams to ensure accurate and timely project execution in a bio/pharmaceutical analysis environment. Employee Responsibilities Audit sample information, including the formal review of all protocols, specifications, methods, and other documents submitted by the client or used by the project within a LIMS system . Manage technical information within a LIMS system relating to Sample Management. Send entry instructions to the sample administration regarding incoming samples. Direct client interaction via email. Communicate with Project Management, Inside/Outside Business Development, and Technical groups as necessary to complete assignments. Communicate regular status updates to supervisor. Qualifications Education: M.Pharm / M.Sc. Experience Level 3 - 5 years in Bio/Pharmaceutical Analysis. Key Candidate Attributes Self-motivation; excellent quality of work and attention to detail. Ability to communicate effectively with coworkers and internal/external clients. Ability to learn new tasks quickly and to move easily from task to task. Ability to handle prioritization and multiple tasks simultaneously. Ability to use a personal computer and learn necessary programs. Good communication skills (oral and written). Organizational ability and good judgment. Science background/education and/or laboratory experience.
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