(Junior)QA Manager / region Gent / Permanent / GMP / ISO13485
Location: BelgiumThe Company
Our client offers innovative brands & products, they create new or alternative ways to make life better and healthier. By focussing on fundamental research & development, They're not only innovative in formula and design, but also in marketing. They match scientific progress with consumer insights.Their goal? To improve not only our lives, but also those of the next generation.
Role Description
You will be working in the Quality team with 2 other colleagues, reporting to the Head of Quality.Responsibilities
Want 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
Requirements
Everything 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 information
OW! 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!
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Diana Prieto Reyes
Opis stanowiska
The Company
Our client offers innovative brands & products, they create new or alternative ways to make life better and healthier. By focussing on fundamental research & development, They're not only innovative in formula and design, but also in marketing. They match scientific progress with consumer insights.Their goal? To improve not only our lives, but also those of the next generation.
Role Description
You will be working in the Quality team with 2 other colleagues, reporting to the Head of Quality.Responsibilities
Want 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
Requirements
Everything 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 information
OW! 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!
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Diana Prieto Reyes
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości / Audyt produkcji