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QC Analyst II - NTO Large Molecules x2

Posted 18/11/2022
£83,200 per annum

Our leading pharmaceutical compay client is looking to hire 2 QC Analyst II to focus on Large Molecules projects on initial 18 months contracts.

Main responsibilities

  • Storage and management of samples

  • Analytical testing and documentation of API/active ingredient/drug/final product/complaints/stability/packaging material samples

  • Ensuring all activities in compliance with cGxP, incl. data integrity

  • Stability (if not centralized)

o Storage and management of tests/samples

o Analytically document stability samples according to cGxP standards

Financial Responsibility:

(Budget, costs, turnover, etc.) • According to financial competence

Impact on the organization Direct impact on the quality, compliance and timely delivery of products

Relevant experience

• Preferred: Previous experience in the laboratory environment of the pharmaceutical industry (quality assurance, production), in relation to aseptic processes.


• Completed training as a laboratory assistant or equivalent training


Basic knowledge of English (oral and written); fluent knowledge of the national language (oral and written)


• Collaboration, result-oriented

  • Administrative activities as well as GMP and HSE-compliant, efficient creation and documentation of standardized tasks in the infrastructure

  • breakthrough analysis; resilience; operational excellence; continuous training; digital and technical know-how

  • laboratory equipment; quality control (QC) testing; quality control sampling; Knowledge of TQM and related industry GxP standards and processes; laboratory excellence; quality decision-making

Pay rate: 35 - 40 CHF per hour.

18 months contract.


Achieva Group Limited