Pharmaceutical Development Specialist

vor 3 Stunden


Basel, Basel-Stadt, Schweiz Randstad Vollzeit

Job Overview

Randstad is seeking a highly skilled Technical Development Specialist to join our team. As a key member of our organization, you will play a vital role in ensuring compliance and quality within our IMP QC operations.

Key Responsibilities:

  • Lead and manage Corrective and Preventive Actions (CAPAs) and actions arising from deviations and GMP inspections
  • Work closely with QC-Capability Leads (QC-CLs) to maintain and improve compliance processes and documentation
  • Develop and update SOPs (Standard Operating Procedures) and other quality documentation as needed
  • Conduct training sessions and workshops to reinforce GMP compliance across the organization
  • Monitor the effectiveness of implemented CAPAs and GMP actions, and present regular reports on CAPA status, trends, and improvement initiatives to senior management

Required Skills and Qualifications:

  • MSc in Pharmaceutics, Analytical Chemistry, or a related field (PhD is an advantage)
  • Minimum of 2 years of experience working in a GMP environment with a strong focus on HPLC and GC analytics
  • Demonstrated expertise in analytical method validation, and troubleshooting
  • Strong knowledge of GMP regulations and guidelines
  • Excellent organizational, communication, and problem-solving skills
  • Ability to work effectively in a fast-paced, team-oriented environment
  • High attention to detail and a commitment to maintaining the highest standards of quality and compliance

Benefits:

  • Opportunity to work with a leading company in the pharmaceutical sector
  • Chance to develop and enhance your skills and expertise in a dynamic and supportive environment
  • Competitive salary and benefits package


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