Qualified Person / Brussel - Elsene / Permanent Contract / 2 - 5 years of experience
Location: BelgiumSIRE® 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 Bruxelles-Capitale Belgium.
- Deviation management
- Product complaint handling
- Notification to management
- Local contractor Quality oversight
- Inspections and Internal Audit
- Oversight of local Repackaging and Relabeling Operations
- Development and Maintenance of Consistent Quality Culture
- Local BU support
o Qualified Person certification according to the Royal Decree of 14 December 2006 article 84 and recognized by the Belgian Agency is an asset.
o Have appropriate quality and technical experience to manage expectations.
o Assess risk and make sound & effective quality decisions under pressure through analysis of data.
o Diplomatic in communication with internal and external customers.
o Show strong negotiation and effective communication skills.
o Self-motivated individual who is comfortable with working independently.
o Able to lead and work effectively in cross-functional team & collaborate.
o French or Dutch and English verbal and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
The Company
Biopharmaceutical client who is dedicated to bring therapies that will significantly improve patients lives.Role Description
The key role of the QP is to maintain, update and continuously improve an appropriate and sustainable Product Quality System and Quality Culture at the client in order to ensure compliance with the company and Regulatory Authority expectations at all time. In absence or by delegation of the QO Lead, the main point of contact, for the investigation and resolution of all (product) quality issues and for interacting with the relevant local stakeholders .Responsibilities
- Product Quality Systems- Deviation management
- Product complaint handling
- Notification to management
- Local contractor Quality oversight
- Inspections and Internal Audit
- Oversight of local Repackaging and Relabeling Operations
- Development and Maintenance of Consistent Quality Culture
- Local BU support
Requirements
o Master Degree in Pharmaceutical Scienceso Qualified Person certification according to the Royal Decree of 14 December 2006 article 84 and recognized by the Belgian Agency is an asset.
o Have appropriate quality and technical experience to manage expectations.
o Assess risk and make sound & effective quality decisions under pressure through analysis of data.
o Diplomatic in communication with internal and external customers.
o Show strong negotiation and effective communication skills.
o Self-motivated individual who is comfortable with working independently.
o Able to lead and work effectively in cross-functional team & collaborate.
o French or Dutch and English verbal and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
