Technical Development Specialist (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Lead and manage CAPAs and actions from deviations, ensuring timely and effective implementation
• Conduct thorouh investigations of deviations to determine root causes and develop appropriate CAPAs. Document all CAPA activities in compliance with GMP regulations and company procedures.
• Maintain inspection readiness by continuously improving compliance processes and documentation
• Work closely with QC-CLs to ensure alignment on CAPA implementation and compliance improvements
• Provide expert guidance and support to QC-CLs in addressing GMP issues and enhancing quality systems
• Identify areas for improvement within the quality systems and lead initiatives to enhance compliance
• 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
• Compile and present regular reports on CAPA status, trends, and improvement initiatives to senior management

• MSc in Pharmaceutics, Analytical Chemistry, or a related field. A PhD is an advantage
• First 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
• Hands-on experience with additional analytical techniques
• Previous experience in a leadership or project management role
• Familiarity with electronic laboratory information management systems (LIMS, LES, SAP)
• English fluent, German advantageous

• You will work in an international environment
• A very renowned company

Ihr Kontakt

Referenznummer
801503/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

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