Pharmaceutical Development Specialist
vor 3 Stunden
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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