QAO / Pharma / Biotech / Region Amsterdam / GMP + GDP + Lean

Bedrijfsnaam: -
Plaatsingsdatum: 11/03/2019
Standplaats: -


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 and Biotechnology organisation, based in Noord-Holland Netherlands.The CompanyOur client is a company that focused on the development of innovative immunotherapies. The company works on engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors.

Our client is currently searching for an talent that will ad value to the development of the European Region. This way the company can help as many patients as possible that are in need.

Role DescriptionYou will be joining a newly formed QA operations team! You will work together with your new team on saving lives, by finding a (better) cure!

But... Our client is not like other companies. The have a unique product, so they search for a Quality Assurance Specialist that is as unique and is able to think outside of the box.

You will be a part of the international team that is located in Amsterdam. One of your jobs will be reporting to the QA Manager EU.

ResponsibilitiesWhat you will be doing if you get the job:
- Review batch-related documentation
- Inspect the product disposition process for EU.
- Complete preparations for product disposition
- Inspect the packaging and shipping process for EU.
- Secure that associated CAPAs are initiated and resolved.
- Secure Change Controls are initiated.
- Use lean thinking for improvement project.
- Help with the implementation and maintenance of the GMP training system in EU.

So that's a hole list, and that will not be all of your responsibilities! Your responsibilities are variable en dynamic. You will help where you are needed and communicating with different department will ensure that there will not be a colleague you do not know.

RequirementsOk, Ok, Ok...

Before deciding this is the best job for generating a lot of experience, it's good to know that our client had a few requirements:
- Minimum of 2 years’ progressive quality or manufacturing experience (Pharm or Bio)
- Knowledge of GMPs, GDP, GMP, CAPAs and Lean principles (U.S. and EU standards)
- Good communication skills in English and Dutch
- Everything is possible mentality
- A team-player, leader and the ability to motivate others

Other informationHave in mind, what makes you unique and different for the job? That's one of the questions you can expect!

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.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :