Make your mark for patients
We are seeking a Visual Inspection Specialist with strong communication & organization skills to join our Quality Control team based in Braine-l'Alleud, Belgium.
About the role :
The main scope of this position is:
1. to write report of identification of particles identified during our manufacturing processes.
2. to lead investigations in term of visual inspection of our injectables products and identification of particles.
3. to manage the QC Visual Inspection team as back-up of the team leader.
4. to support audit and product launches (data sharing with authorities, updates of batches, sampling plan, etc).
5. to handle actions, deviations and realize investigations in close collaboration with QA team members.
6. to smoothly communicate with stakeholders about the leadtimes and the investigations.
Who you’ll work with:
You'll join a dynamic and experienced team dedicated to maintaining the highest standards of quality and safety in pharmaceutical product manufacturing.
What you will do :
7. You apply the company's Health and Safety policy.
8. You ensure a safe working environment to meet campus safety objectives.
9. You increase team’s competency by ensuring adequate training, coaching and development of team members in function of the team and people potentials.
10. You ensure the day-to-day operational planning and coordination in order to satisfy the client needs based on a montly forecast.
11. You ensure required corrective actions are taken and put in force.
12. You implement, follow-up and communicate on KPI with its related corrective actions.
13. You inform stakeholders and/or head of the department if deviations from the day-to-day-planning occur.
14. You are prepared and participate actively to weekly/monthly planning meetings, propose solutions, demonstrate creativity and pro-activity to ensure adherence to plan and performance.
15. You are accountable for a pro-active collaboration with different stakeholders.
16. You support the general objectives of the QC Visual Inspection, Devices & Packaging department in accordance with the company’s objectives and formally assess the results with the adequate KPI (Key Performance Indicators) : safety, quality, lead time, social and environment.
17. You participate / do the update of procedures and instructions.
18. You ensure Follow-up or is responsable of corrective actions and preventive actions.
19. You participate to the preparation, the follow-up and the realization of the audits.
20. You ensure adequate training/coaching of the team members.
Interested? For this role we’re looking for the following education, experience and skills :
21. You are fluent in English and French
22. You have a Bachelor's Degree in the field of chemistry, biochemistry, biotechnology,…
23. A previous experience in a similar role is an asset.
24. You have the capacity to cope with change management, high sense of empathy and the capacity to motivate and make people grow through proper training and delegations.
25. You are capable to make one’s proper decisions by utilizing strong analytical skills, troubleshooting and problem-solving approach.
26. You can smoothly communicate and work with technicians, managers, and stakeholders, to lead and influence people in a complex matrix environment.
27. You can manage interfaces with stakeholders (development, quality assurance and analytical product owner,…) and escalade road blockers or any information.
28. You have presentation and meeting facilitation skills.
29. You are customer and results oriented.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!