QA Specialist / Pharma / Temporary / nearby Breda / GMP

Bedrijfsnaam: -
Plaatsingsdatum: 09/04/2019
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-Brabant Netherlands.The CompanyOur client is a professional organisation, based in Noord-Brabant Netherlands. A leading biotechnology companies who's mission is to discover and innovate medicines for patients with serious illnesses.

Role DescriptionSupporting the product complaint system at Amgen through; leading and managing product complaint investigations, performing data analysis and trending of complaint information to proactively detect signals and take appropriate actions in a timely manner.

Responsibilities- Update the complaints database as soon as factual information is available and summarize closed investigations into the database accurately.
- Ensure complaint related investigations are concise, clear and science-based by reviewing and approving such investigations.
- Follow-up on corrective actions derived from investigations through completion.
- On occasion, depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation.
- Communication and escalation of complaints, site representation on the product complaint network

Requirements- Excellent writing skills to minimize the gap between a highly technical investigation into a simple and concise document that can be understood by non-technical reviewers;
- MSc. or BSc. in the Life Sciences;
- Minimum of 2 years of working experience related to the function;
- Strong project management skills;
- Team-oriented, matrix environment and work effectively with diverse departmental groups
- Customer service skills to operate and deliver results in a matrix-managed GMP environment.
- Computer literacy, independently understand

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 :