Sr. Quality Assurance Officer / Perm / Pharma / Full-time / nearby Utrecht / GMP, GCP and GLP

Bedrijfsnaam: -
Plaatsingsdatum: 05/03/2019
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 Utrecht Netherlands.The CompanyOur client is a clinical-stage company developing innovative antibody therapeutics. The innovative antibody therapeutics are manufactured using industry standard processes and have been observed in pre-clinical studies.

It's a interesting company, they are searching for interesting people!

Role DescriptionFor the Quality Assurance team our client is searching for a Sr. Quality Assurance Associate. Together with the team you support projects relating to the development of our client clinical products. As a member of their small QA team, you will have a significant impact when it comes to promoting quality and compliance, and you will be exposed to a very broad range of QA activities from GMP and GCP to GLP. This is a role for an experienced QA professional!

Do you like to keep on learning and be involved in many activities? Do you have a proven project management track record?
Then you are the one they are looking for!

ResponsibilitiesIf you are considering the job, it's is handy to know your responsibilities:
- Providing QA advice
- Oversight to different kinds of projects (investigational products);
- Managing quality processes (improve the internal Quality Management System)
- Ensure GXP compliance;
- Contractor management (audits, quality agreements);
- GXP-related activities QA-standard activities (including method validations, internal audits, changes, deviations, CAPAs, training, documentation on GXP operations, stability, and release of batches for clinical use).

RequirementsWhat do you need to have for the job...?

- You need to have a MSc. Biosciences or in the pharmacy;
- You need to have 6-8 years of QA experience in GMP and/or GCP;
- You need to have experience in developing quality systems and auditing GXP contractors;
- You need to be quality and compliance driven, eager to learn.
- You need to have strong analytical skills;
- You are fluent in English;
- Knowledge of the German and/or Chinese language is a plus;
- Willingness to travel up to 15% of the time.

Other informationOur client offers a competitive salary and flexible working hours. Our client also offers an excellent pension scheme, company bonus, and 30 days’ annual holiday based on a full-time position.

Are you the one for this role? Don't wait or hesitate...Apply!

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 :
5 - 10 jaar
Contactgegevens :