IT Project Coordinator in Quality Assurance
Keyrus Life Science is looking for an IT Project Coordinator to support our client’s Quality Assurance (QA) department in authoring and maintaining the IT System documentation. For this purpose, you are going to be in charge of the IT System documentation ensuring its Design Specification, Configuration Specification, Functional Specification, etc. You will manage the review and approval of workflows of those documents and support developers during the implementation. Moreover, you will coordinate the test matrix, ensuring the execution and documentation and analysing the possible defects. As an IT Project Coordinator, you will communicate with IT and non-IT stakeholders and act as an Analyst on QA related projects (small to medium, in a GxP environment).
You have a strong IT background (Computer Science or related technical discipline) and you already gained a minimum of 3 years’ experience in the pharmaceutical/biopharmaceutical sector to be able to understand the needs and how the system works. You are knowledgeable about core Quality Assurance processes in a GxP pharmaceutical environment. You are detail-oriented and focused on quality in your day-to-day work. You have a working knowledge of Computer System Validation (CSV) and you master TrackWise, Veeva, Analytics with Cognos or QlikSense. As an IT Project Coordinator, you have strong interpersonal, oral and written communication skills in order to collaborate with different members of Global QA, IT Compliance as well as other IT or Business functions. Fluency in English is mandatory, fluency in French is a strong plus.
We offer you a permanent contract and after an on-boarding at Keyrus Life Science, a full-time assignment at our client’s site in Braine-l’Alleud is already waiting for you!
What we offer
At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.
We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.
Who we are
Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
Keyrus Belgium Offices:
- Office Park Waterloo - Drève Richelle 161 - 1410 Waterloo
- Nijverheidslaan 3, - Strombeek-Bever