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Senior Quality Assurance Specialist.

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For our client, an internationally-active pharmaceutical company, specializing in niche areas such as hematology and oncology, we are looking for a:

Senior Quality Assurance Specialist
Location: Basel-Country
Contract: permanent

Your tasks:
Your main responsibilities will include:
  • Managing the Quality Management Manual documentation independently
  • Monitoring and tracking complaints, deviations, and resulting measures (CAPA)
  • Implementing changes (Change Control) within the quality assurance system
  • Conducting and accompanying internal and external audits and their documentation
  • Supporting quality-relevant aspects in projects as Project Quality Manager
Your role is crucial in driving the continuous improvement of our client's processes and their implementation, contributing to their commitment to excellence in the pharmaceutical industry.

Requirements
To be considered for this role, you must have:
  • An educational background in a science-related field (BSc, MSc or PhD)
  • Minimum of 3 years of professional experience in quality assurance within a GMP-regulated company, preferably in the pharmaceutical industry
  • Proficient in MS Excel and MS Word
  • Fluency in both German and English
Additionally, it's advantageous if you have:
  • Experience working in a regulated environment or quality assurance system (ISO 9001, GMP)
  • Database knowledge
  • Knowledge of additional languages

For our client, an internationally-active pharmaceutical company, specializing in niche areas such as hematology and oncology, we are looking for a:

Senior Quality Assurance Specialist
Location: Basel-Country
Contract: permanent

Your tasks:
Your main responsibilities will include:
  • Managing the Quality Management Manual documentation independently
  • Monitoring and tracking complaints, deviations, and resulting measures (CAPA)
  • Implementing changes (Change Control) within the quality assurance system
  • Conducting and accompanying internal and external audits and their documentation
  • Supporting quality-relevant aspects in projects as Project Quality Manager
Your role is crucial in driving the continuous improvement of our client's processes and their implementation, contributing to their commitment to excellence in the pharmaceutical industry.

Requirements
To be considered for this role, you must have:
  • An educational background in a science-related field (BSc, MSc or PhD)
  • Minimum of 3 years of professional experience in quality assurance within a GMP-regulated company, preferably in the pharmaceutical industry
  • Proficient in MS Excel and MS Word
  • Fluency in both German and English
Additionally, it's advantageous if you have:
  • Experience working in a regulated environment or quality assurance system (ISO 9001, GMP)
  • Database knowledge
  • Knowledge of additional languages

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AB

Audrey Bisch

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