QA Lead / Pharma / Belgium / Region Brussel / GMP + GDP / RIN
Location: NetherlandsSIRE® 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 Netherlands.
Are you the superhero that is going to make a difference for the patients?
- Be an internal consultant for key regulatory topics
- Editing GMP/GDP content
- Be the GMP/GDP RIN leader and work wih the other leaders.
- Managing GMP/GDP/Device/CMC
- Developing and executing tools
- Strong organizational and project management skills
- Fluent English is a must
- High degree of independence
- Minimum 8 years working in the life science industry
- Minimum 5 years working in quality assurance
- Experience with GMP regulation
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.
The Company
Our client and their employees puts their hearts, souls and high potential skills into making a difference for patients! They work together to accomplish the impossible and they push the boundaries so they can discover innovation. To strengthen their Quality Assurance department, our client is looking to fill the position of a QA Lead.Are you the superhero that is going to make a difference for the patients?
Role Description
As a new employee you will manage changes specific to GMP/GDP. Also will you coordinate the GXP RIN program. You will be responsible for the contact with the stakeholders and experts internally and externally of our client.Responsibilities
Your responsibilities are as followed:- Be an internal consultant for key regulatory topics
- Editing GMP/GDP content
- Be the GMP/GDP RIN leader and work wih the other leaders.
- Managing GMP/GDP/Device/CMC
- Developing and executing tools
Requirements
To be a part of this amazing team and company you need to have:- Strong organizational and project management skills
- Fluent English is a must
- High degree of independence
- Minimum 8 years working in the life science industry
- Minimum 5 years working in quality assurance
- Experience with GMP regulation
Other information
Are you the hero they need? Apply and try!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.
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