QP / Pharma / Temporary / region Utrecht / BIG-register / GMP
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, Biotechnology and Clinical Research organisation, based in Utrecht Netherlands.
Sounds interesting, does'n it?
Big responsibilities with great communication skills... For those who loves to socialize!
- ...the training of employees.
- ...the contribution to the policy aspect, the further development and the maintenance of the quality system.
- ...taking care of improving the quality management and production processes.
- ...various improvement projects.
Our client is searching for an enthusiastic Quality Person who is registered in the BIG-register. As Quality Person you have substantive knowledge of production of medicines in a hospital or industrial environment. Having experience in the field of GMP production of cell and gene therapies is a big plus!
As Quality Person you need to have knowledge of the relevant legislation and regulations. You need to be customer-oriented and a real team player. This requires good communication skills.
Our client attach great importance to an independent, accurate, structured working method where you dare to take decisions. It's a temporary job, based on 36 hours a week for a year with possibility of extension.
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 is looking for a Qualified Person. Our client constantly raises the bar. The result is innovative, leading treatments that meet the care needs of today and the future.Sounds interesting, does'n it?
Role Description
As a Quality Person you work closely with the staff of the subsection Clinical Medicines Research, the subdepartment Preparations, the Cell Therapy Facility and analysts of the laboratory pharmaceutical quality control. You report to the Head of Safety and Quality.Big responsibilities with great communication skills... For those who loves to socialize!
Responsibilities
As a Quality person you release research medicines, both the traditional medicines and the ATMPs. You also carry out work in the field of Quality Assurance (QA). You have a leading role in quality management, including the preparation and assessment of deviations, changes, validation reports, QA agreements and management reviews. You are responsible for...:- ...the training of employees.
- ...the contribution to the policy aspect, the further development and the maintenance of the quality system.
- ...taking care of improving the quality management and production processes.
- ...various improvement projects.
Requirements
What are you waiting for? Read the requirements and Apply!Our client is searching for an enthusiastic Quality Person who is registered in the BIG-register. As Quality Person you have substantive knowledge of production of medicines in a hospital or industrial environment. Having experience in the field of GMP production of cell and gene therapies is a big plus!
As Quality Person you need to have knowledge of the relevant legislation and regulations. You need to be customer-oriented and a real team player. This requires good communication skills.
Other information
Are you the one?Our client attach great importance to an independent, accurate, structured working method where you dare to take decisions. It's a temporary job, based on 36 hours a week for a year with possibility of extension.
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.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
