Validation expert in Mannheim wanted! Are you interested? With the many benefits at our subsidiary GULP solution services, such as competitive compensation and retirement plans, you certainly can't say "no". If that's the case, apply today for the available position at a pharmaceutical company! Here's another advantage: Applying with us is absolutely straightforward, requiring only your name, email address, and resume. People with disabilities are warmly welcomed at our company.
Das dürfen Sie erwarten
* Option of permanent employment with our business partner
* Extensive social benefits, incl. Christmas and holiday bonuses
* Up to 30 days vacation per year
* Free online courses
Ihre Aufgaben
* Performing activities as required to meet Q&R goals and objectives independently and being able to identify improvements and implement with collaboration from the manager
* Document authoring and review as required to support changes
* Perform technical reviews as applicable
* May require collaboration with supervisor on technically complex technical reviews independently
* Preparing documentation for and participating in audits as applicable
* Responsible for training, coaching and mentoring other quality managers or business partners, as applicable in a professional manner to ensure that business needs are being met
* Able to troubleshoot issues as they arise, develop and independently implement solutions to ensure that daily work is completed without jeopardizing compliance
* Communicating significant quality or regulatory issues and risks that may impact product quality or regulatory compliance in a timely manner to Executive Management
Unsere Anforderungen
* Completed Master's degree in natural sciences (e.g. chemistry, biotechnology or pharmacy), alternatively a completed Bachelor's degree in natural sciences with professional experience in a comparable field
* Profound work experience in the GMP environment, ideally in quality assurance and/or quality control in dia- and/or pharmaceutical sector
* Good knowledge of analytical and method development/validation as well as process and method transfer
* Good knowledge of cleaning processes
* Experience in the preparation of process risk analyses and good process understanding
* Ensure implementation of regulatory requirements and review of above validation documents and inspection and test plans
* Experience in the creation or evaluation of process risk analyses
* Knowledge of deviation management and change control
* Good knowledge of MS Office and Google applications (e.g. G Suite)
* Very good English skills (for meetings and documentation)
* Ability to work in a team and experience in agile working