Quality Specialist GMP

Quality Specialist GMP (m/f/d) Your next career move in pharmaceutical quality awaits you Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a GMP-regulated environment where precision and compliance meet innovation? Join a dynamic team and make a real impact in bringing life-changing therapies to patients worldwide. Duration: 01.01.2026 to 30.06.2026 (extension possible based on fincancial approval)Location: BaselType: Temporary positionRemote Working: NoPay Rate: CHF 34/h to CHF 43/h About our client For our client, a globally recognized pharmaceutical company specializing in cutting-edge oncology and ophthalmology treatments, we are seeking a dedicated Quality Specialist (m/f/d). This innovative organization is at the forefront of developing novel therapies and maintains the highest cGMP standards in their state-of-the-art facilities in Basel. With a strong commitment to quality excellence and patient safety, they offer a collaborative environment where your expertise will directly contribute to advancing healthcare. Your responsibilities Review and release GMP documentation including batch records, packaging documents, and investigational medical product files to ensure regulatory complianceFacilitate timely batch release of labels, primary packaging materials, and clinical trial supplies according to strict quality standardsProvide functional expertise to cross-functional teams and support quality assurance activities across the technical research and development unitManage document workflows by receiving, scanning, filing, and archiving quality-critical documentation such as Certificates of Compliance and review checklistsContribute to quality improvement projects including tool development, process optimization, quality risk assessments, and validation activitiesEnsure cGMP adherence by applying internal SOPs, regulatory guidelines, and health authority requirements in all quality-related tasksSupport qualification activities for facility upgrades, IT validation projects, and implementation of quality management systems Your profile Technical or scientific education with a Bachelor's degree and minimum 3 years of pharmaceutical/biotech experience, or Technician diploma with at least 5 years of relevant experienceSolid cGMP knowledge and understanding of regulatory requirements in pharmaceutical quality assurance and batch release processesExperience in GMP documentation review, batch record evaluation, or quality control in a regulated pharmaceutical environmentStrong communication skills to effectively collaborate with production, quality control, and cross-functional teams on compliance mattersFluent English (written and spoken) is essential; proficiency in German is advantageousOrganizational excellence with the ability to manage multiple priorities and meet critical deadlines in a fast-paced environmentBasic understanding of drug development processes and investigational medicinal product manufacturingCompleted GMP training or willingness to undergo comprehensive training before task assignment What nemensis offers you Nemensis AG is your specialized personnel consultant in the Life Sciences sector with headquarters in BaselComprehensive consultation and support throughout the entire application process by our experienced consultantsAccess to an extensive client network and exciting opportunities in Northwestern SwitzerlandFast and uncomplicated entry through individual guidance and professional advice during the application process Ready to elevate your quality career?At nemensis ag, we've connected thousands of professionals with their dream jobs, giving 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 We're looking forward to hearing from you for the position as Quality Specialist GMP (m/f/d) in Basel. Apply now and become part of a team that sets the standard in pharmaceutical quality  Branche: Pharma-IndustrieFunktion: QualitätsprüfungAnstellungsart: Temporäre ArbeitKarrierestufe: Angestellte/r