QC Support Specialist (All genders).
- Entreprise
- Randstad (Schweiz) AG
- Lieu
- Vevey
- Date de publication
- 29.04.2024
- Référence
- 4603562
Description
- Vevey, Vaud
- Temporär
- CDD de 8 mois
Job Details
Your role:
QC Sampling activities:
- Improve the standard time via continuous improvement projects and realization of the activities
- To support and improve the interface with external labs (sample shipment & results handling)
- To support the sampling team in some operational activities (sample reception, aliquoting, worklist corrections)
QC Compliance activities:
- Lead the deviations related to our activities
- Trainer for compliance and operational activities
- Participation in the governance of the compliance community
General and Project Management :
- To ensure adherence to the detailed planning by all stakeholders,
- To ensure KPIs target are reached,
- To ensure compliance during deployment and hyper-care phases,
- To ensure final user's adherence,
- To build detailed deployment and hyper-care planning,
- To monitor activities progress
- To lead and support project team for deployment activities,
- To raise and follow CCP,
- To build change management plan,
- To react on and resolve all technical issues involving the group autonomously in a timely and positive manner,
- Be an actor of the continuous improvement initiatives using a lean process mindset,
- To strongly participate in the management of our performance meeting and contribute to improve it.
Your role:
QC Sampling activities:
- Improve the standard time via continuous improvement projects and realization of the activities
- To support and improve the interface with external labs (sample shipment & results handling)
- To support the sampling team in some operational activities (sample reception, aliquoting, worklist corrections)
QC Compliance activities:
- Lead the deviations related to our activities
- Trainer for compliance and operational activities
- Participation in the governance of the compliance community
General and Project Management :
- To ensure adherence to the detailed planning by all stakeholders,
- To ensure KPIs target are reached,
- To ensure compliance during deployment and hyper-care phases,
- To ensure final user's adherence,
- To build detailed deployment and hyper-care planning,
- To monitor activities progress
- To lead and support project team for deployment activities,
- To raise and follow CCP,
- To build change management plan,
- To react on and resolve all technical issues involving the group autonomously in a timely and positive manner,
- Be an actor of the continuous improvement initiatives using a lean process mindset,
- To strongly participate in the management of our performance meeting and contribute to improve it.
Qualifikationen
Who you are:
- Eng. in sciences (chemistry, Biology.) or at least 1 year of experience in GMP environment
- At least 1 year expertise in Biotech Industry
- Experience in Quality Control and Quality systems
- Experience in planification tools is a plus
- Knowledge in RFID principle is a plus
- Good knowledge in visual management
- Knowledge of applicable cGMPs
- Fluent in French & English
- Process mindset with the appropriate level of customer service
- Able to understand in detail all the activities carried out in the group and its role in the context of the overall site and QC processes
- Able to react and resolve all human & technical issues involving the group autonomously in a timely and positive manner, with an efficient solution
- User of the Problem-Solving tool and ensure its use in the group
- Result driven and a 'can do' attitude, helping organization to deliver stretch goals on lead time
- Autonomous and reliable, highly motivated
- Customer oriented
- Collaborative and positive communication within the team and with partners / customers
- Seeking for proactive implementation of new technologies, new good practices and continuous improvement for the team
