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Project Analyst NPI (all genders) | Befristeter Vertrag für 2 Jahre | (Vollzeit)

Ludwigshafen, RP, de💼 Full-time🗓 2026-09-01 → 2026-09-26

Core

Ensure and execute GMP-compliant testing of intermediate products, bulk/final pharmaceuticals, and stability samples.

Role type

Senior IC pharmaceutical quality analyst

Builds

Validated test results and stability data for pharmaceutical manufacturing

Domain

Life sciences / Pharmaceutical manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

HPLC, UV/VIS spectrometry, Bioanalytical methods (ELISA, Reporter Gene Assays), GMP documentation, chemical reagent management, analytical problem solving

Preferred skills

Method validation, method transfer, new technique implementation

Technologies

HPLC, UV/VIS spectrometry, ELISA, Reporter Gene Assays

Responsibilities

Execute established and specialized analytical methods independently, plan and conduct validations and method transfers, evaluate and document results ensuring traceability and accuracy, manage procurement of chemicals and consumables, solve analytical problems proactively

Seniority

Senior, hands-on IC

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