Talent.com
Diese Stelle ist in deinem Land nicht verfügbar.
Technical Developer Quality Lead (f / m / d)

Technical Developer Quality Lead (f / m / d)

GULP – experts unitedHolzkirchen, Oberbayern
Vor 30+ Tagen
Stellenbeschreibung

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 development
  • Proactively support and collaborate with key stakeholders to ensure clinical Quality-by-Design for the projects under responsibility
  • Establish and lead core Quality Issue Management governance for critical or major quality issues pertinent to the programs being assigned and ensure timely escalation when required
  • Provide regulatory guidance to day to day questions arising from Clinical trials deliverables
  • Collaborate with key stakeholders to drive initiatives relevant to internal monitoring and dispense strong Quality oversight for outsourced activities
  • Support inspection preparation and facilitation in collaboration with other QA groups including but not limited to Regulatory Affairs Quality and Compliance
  • Participate in audits and inspections, as applicable, and follow-up activities including CAPA preparation and implementation
  • Provide lessons learned from deviations and incidents, audits and inspections
  • Actively leverage audit and inspection outcomes and trends to sustain improvement in clinical trials conduct
  • Act 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 processes
  • Your profile

  • Several years of solid experience in regulated activities, GCP and GLP, preferably in QA positions
  • Experience from positions in clinical development and / or compliance, with strong quality mindset in focus
  • Several years experience in managing projects, preferably from Clinical Quality Assurance perspective
  • Solid understanding of global expectations of Health Authorities in the area of Clinical Development and pro-found understanding of the science of product development
  • Ability to work independently in a global and matrix environment
  • Strong skills in GCP, quality or clinical development
  • Strong interpersonal, communication, negotiation, and problem solving skills
  • Fluency in English and German oral and written