Ready to shape the future of pharmaceutical analytics? - Duration: 04/08/2025 to 31/08/2027 - Location: Basel, Switzerland (on-site position) - Type: Temporary Assignment - Salary: CHF 38,75/h - 57,50/h - ID: 01633 About Our Client For our client, a leading pharmaceutical company in the Basel region, we are seeking a dedicated professional. This innovative organization is at the forefront of drug development and analytical research, specializing in small molecule therapeutics and cutting-edge radioligand therapy solutions. The company plays a crucial role in advancing healthcare through state-of-the-art analytical technologies and maintains a strong position in the global pharmaceutical market. Your Responsibilities - Execute and oversee comprehensive analytical experiments for drug substances and drug products, ensuring compliance with cGMP standards and agreed timelines - Document and manage raw data submission in appropriate laboratory information management systems (LIMS) with meticulous attention to detail - Maintain excellence in laboratory practices and documentation standards during all analytical activities - Investigate and evaluate analytical results, including troubleshooting stability test failures and out-of-specification deviations - Review and approve critical analytical documentation including raw data assessments, validation protocols, and method specifications - Mentor and guide laboratory associates, fostering scientific excellence and knowledge transfer - Collaborate effectively with internal teams and external stakeholders to ensure seamless project execution - Support regulatory activities including audits and health authority inspections, maintaining zero critical findings within assigned scope Your Profile - Master's degree in analytical chemistry or equivalent field with minimum 5 years of pharmaceutical industry experience - Proven expertise in advanced analytical techniques including HPLC, particle size analysis, dissolution testing, cleaning validation, X-Ray, and IR spectroscopy - Solid GMP experience with demonstrated knowledge of regulatory requirements and quality standards - Experience in raw data review and approval processes with strong attention to regulatory compliance - Handling of deviations and out-of-specification investigations considered a valuable asset - Excellent English proficiency (written and verbal); German language skills advantageous - Strong analytical mindset with ability to work independently in a fast-paced environment Advantages of nemensis - nemensis AG is your specialized personnel consultant in the Life Sciences sector with headquarters in Basel - Comprehensive consultation and support throughout the application process by our experienced consultants - Access to an extensive client network and exciting positions in Northwestern Switzerland - Fast and uncomplicated entry through individual guidance and consultation in the application process Take the Next Step in Your Career At nemensis ag, we have already connected thousands of applicants with their dream jobs and given them the opportunity to develop further or re-enter the job market. What can we do for you and your career today? Get in touch with us! Branche: Pharma-Industrie Funktion: Forschung und Entwicklung Anstellungsart: Temporäre Arbeit