Their goal? To improve not only our lives, but also those of the next generation.
Role DescriptionYou will be working in the Quality team with 2 other colleagues, reporting to the Head of Quality.
ResponsibilitiesWant to get experienced? This is the job to boost your career.
- Support the Design Transfer of new products to Operations - Daily contacts/follow-up of suppliers (subcontractors): Compiling all documentation, necessary for production and QC of final products, approval of master batch records, deviation handling, follow-up process validation - Release of Final Products to the customer - Follow-up of stability studies - Customer Complaint Handling (Investigation, Report, Follow-up) - Initiate and follow-up CAPA reports
RequirementsEverything has his requirements, but if you match, you are the one!
- Knowledge of GMP and/or ISO13485 standard - Minimum 2 years of experience in a similar role in a Pharmaceutical Company - You have a Master’s degree (Pharma, Sciences, Bio..) - Experience in a Production Environment is a plus - You are fluent in Dutch and English - You have a mature personality. You are assertive and like challenges. You are passionate and have strong organizational and analytical skills.
Other informationOW! You need to have a proactively mindset and be solution-oriented. And last but nor least, you are a team player. Through your excellent communication skills, you ensure optimal cooperation within the company with the other departments!
So do you have what it takes? Apply!
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.