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QC Analyst

Switzerland   •  £32 - £35 per hour  •  Contract/Temporary, Full time


Our leading pharmacutical client is looing to hire a QC Analyst on an initial 7 month contract in Basel.

QC Analyst I

Department: Quality

Job Purpose

Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.

Major Accountabilities

Operational

? Sample storage and management
? Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
? Ensure all activities in compliance with cGxP, incl. data integrity
? Stability (when not centralized)
o Testing/Sample storage and management
o Analytical documentation of stability samples to cGxP standards

HSE

? Comply with all HSE guidelines
? Detect and report potential accident, risks and propose solutions
? Responsible for participating in initial training and retraining

Key Performance Indicators (Indicate how performance for this role will be measured)

? Orders are processed correctly and quickly
? no waiting times due to wrong or delayed order
? Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time
? Ensure constant readiness for inspection, no critical complaints from superiors and inspectors
? Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities
? Finding and implementing optimization options to reduce costs
? Completed training plan.

Functional: See organizational chart

Financial responsibility:
(Budget, Cost, Sales, etc.) ? According to financial responsibility

Impact on the organization Direct impact on Quality, compliance, and product timely delivery

Ideal Background (State the preferred education and experience level)

Relevant Experience ? Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique.

Education & Qualification ? Completed apprenticeship as a laboratory assistant or equivalent training

Languages Basic (oral and written) in English; fluent in local language (oral and written)

Competencies ? Collaboration; result-oriented
? Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
? Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
? Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making

  • Agency: Achieva Group Limited
  • Reference: BH-33946-1
  • Posted: 23rd November 2022
  • Expires: 21st December 2022

Achieva Group Limited

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