(Junior) Quality Manager
Location: BelgiumThe Company
.Role Description
You will be working in a rapidly expanding company where innovation is key to make the next step. You are a person who has excellent communication skills, you have a minimum of two years experience in a similar role, you have knowledge of ISO 13485 and you are used to being the point of contact of customersResponsibilities
- 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
Requirements
- 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.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
Job Description
The Company
.Role Description
You will be working in a rapidly expanding company where innovation is key to make the next step. You are a person who has excellent communication skills, you have a minimum of two years experience in a similar role, you have knowledge of ISO 13485 and you are used to being the point of contact of customersResponsibilities
- 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
Requirements
- 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.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control