Do you want to progress professionally and desire a job where you are challenged and supported? With regular working hours, good benefits, and diverse opportunities for further development? Then you've come to the right place : Our subsidiary Randstad professional solutions offers an attractive position as technical developer quality lead at a pharmaceutical company in Holzkirchen . Apply online right away. We value equal opportunities and welcome applications from people with disabilities.
Here's what we offer
- Up to 30 days vacation per year
- Option of permanent employment with our business partner
- Extensive social benefits, incl. Christmas and holiday bonuses
Your tasks
Provide robust and clear quality oversight in the following areas of clinical developmentProactively support and collaborate with key stakeholders to ensure clinical Quality-by-Design for the projects under responsibilityEstablish and lead core Quality Issue Management governance for critical or major quality issues pertinent to the programs being assigned and ensure timely escalation when requiredProvide regulatory guidance to day to day questions arising from Clinical trials deliverablesCollaborate with key stakeholders to drive initiatives relevant to internal monitoring and dispense strong Quality oversight for outsourced activitiesSupport inspection preparation and facilitation in collaboration with other QA groups including but not limited to Regulatory Affairs Quality and ComplianceParticipate in audits and inspections, as applicable, and follow-up activities including CAPA preparation and implementationProvide lessons learned from deviations and incidents, audits and inspectionsActively leverage audit and inspection outcomes and trends to sustain improvement in clinical trials conductAct as the point of contact for quality assurance in the defined development projects and audits, attending the relevant meetings and ensuring that quality is included in the decision-making processesYour profile
Several years of solid experience in regulated activities, GCP and GLP, preferably in QA positionsExperience from positions in clinical development and / or compliance, with strong quality mindset in focusSeveral years experience in managing projects, preferably from Clinical Quality Assurance perspectiveSolid understanding of global expectations of Health Authorities in the area of Clinical Development and pro-found understanding of the science of product developmentAbility to work independently in a global and matrix environmentStrong skills in GCP, quality or clinical developmentStrong interpersonal, communication, negotiation, and problem solving skillsFluency in English and German oral and written