QA Release Engineer / Freelance / Pharma / East Flanders
Location: BelgiumThe Company
They are a worldwide company in the biotechnological field. They focus on ensuring the safety and quality of medicines, vaccines and health care products.Role Description
It is your passion to ensure the safety and quality of their health care products? Do you want to be a part of an important team that contributes on the continuous improvement of those health care products? Are you willing to do an extra step to make sure everything gets done on time? Then this is the job for you! This job will last for 6 months with the possibility to extend.Responsibilities
You will be responsible for Reviewing documents and releasing products. You will be involved during the audits and ensuring the guidelines are followed. Next to that you will be responsible for the following:- Implementing new processes to improve and ensure this quality
- Maintaining contact with colleagues from production and participate in the daily operational consultation
- Contribute to the existing projects within multidisciplinary teams
Requirements
- BSc or MSc within the biotechnology or pharmaceutical industry- You have experience with recalls and reviewing
- Experience in the pharmaceutical industry and in particular knowledge of GMP
- Knowledge of the relevant computer systems such as Trackwise and SAP
- You have experience with GMP
- Dutch and English are required
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
Job Description
The Company
They are a worldwide company in the biotechnological field. They focus on ensuring the safety and quality of medicines, vaccines and health care products.Role Description
It is your passion to ensure the safety and quality of their health care products? Do you want to be a part of an important team that contributes on the continuous improvement of those health care products? Are you willing to do an extra step to make sure everything gets done on time? Then this is the job for you! This job will last for 6 months with the possibility to extend.Responsibilities
You will be responsible for Reviewing documents and releasing products. You will be involved during the audits and ensuring the guidelines are followed. Next to that you will be responsible for the following:- Implementing new processes to improve and ensure this quality
- Maintaining contact with colleagues from production and participate in the daily operational consultation
- Contribute to the existing projects within multidisciplinary teams
Requirements
- BSc or MSc within the biotechnology or pharmaceutical industry- You have experience with recalls and reviewing
- Experience in the pharmaceutical industry and in particular knowledge of GMP
- Knowledge of the relevant computer systems such as Trackwise and SAP
- You have experience with GMP
- Dutch and English are required
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met 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