Senior QA Consultant (Freelance)
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Antwerpen Belgium.
- Handle cancelations, reviewing and investigating
- Train employees in GMP activities
- Generate and review SOP’s
- Supporting CSCM
- Participate in different projects and global Quality initiatives
- Knowledge of GMP, GDP and/ or GCP
- 3-5 years of experience in related area
- Experience with the processes
- Fluent in English and Dutch is preferred
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
The Company
The company is an international organization who focus on a medical need for a better life of people by producing medicines. This to help patients with different diseases.Role Description
Currently we are looking for a talented and ambitious QA Senior Associate Consultant. You will be responsible for the whole process of the incoming materials and products. Furthermore, you will function as a point of contact for different departments and their requirements. The duration of this project is ± one year.Responsibilities
Your responsibility is to support the QA for clinical products. You will make sure that the requirements will be performed to deliver the right product batches. This has to be GMP compliance. Look into the in- and out coming distribution and resolve complaints.- Handle cancelations, reviewing and investigating
- Train employees in GMP activities
- Generate and review SOP’s
- Supporting CSCM
- Participate in different projects and global Quality initiatives
Requirements
- BSc. or MSc. in life science related field or equivalent- Knowledge of GMP, GDP and/ or GCP
- 3-5 years of experience in related area
- Experience with the processes
- Fluent in English and Dutch is preferred
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
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Job Description
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Antwerpen Belgium.
- Handle cancelations, reviewing and investigating
- Train employees in GMP activities
- Generate and review SOP’s
- Supporting CSCM
- Participate in different projects and global Quality initiatives
- Knowledge of GMP, GDP and/ or GCP
- 3-5 years of experience in related area
- Experience with the processes
- Fluent in English and Dutch is preferred
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
The Company
The company is an international organization who focus on a medical need for a better life of people by producing medicines. This to help patients with different diseases.Role Description
Currently we are looking for a talented and ambitious QA Senior Associate Consultant. You will be responsible for the whole process of the incoming materials and products. Furthermore, you will function as a point of contact for different departments and their requirements. The duration of this project is ± one year.Responsibilities
Your responsibility is to support the QA for clinical products. You will make sure that the requirements will be performed to deliver the right product batches. This has to be GMP compliance. Look into the in- and out coming distribution and resolve complaints.- Handle cancelations, reviewing and investigating
- Train employees in GMP activities
- Generate and review SOP’s
- Supporting CSCM
- Participate in different projects and global Quality initiatives
Requirements
- BSc. or MSc. in life science related field or equivalent- Knowledge of GMP, GDP and/ or GCP
- 3-5 years of experience in related area
- Experience with the processes
- Fluent in English and Dutch is preferred
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 / Production Audit