Descripción
Critères de l'offre
* Métiers :
* Quality control Director
* Expérience min :
* 6 à 10 ans
* Diplômes :
* No Diploma
* Compétences :
* English
* French
* Lieux :
* Neuchâtel
* Conditions :
* Permanent contract
* Full Time
Critères de l'offre
* Métiers :
* Quality control Director
* Expérience min :
* 6 à 10 ans
* Diplômes :
* No Diploma
* Compétences :
* English
* French
* Lieux :
* Neuchâtel
* Conditions :
* Permanent contract
* Full Time
## L'entreprise : LHH ##
**The Adecco Group Switzerland**
Plus d'infos sur LHH
## Description du poste ##
LHH Recruitment Solutions is a specialized talent recruitment agency. We provide tailored services to help companies find the best candidates for their staffing needs.
With deep industry expertise and a commitment to excellence, LHH RS is a trusted partner in Switzerland for many years.
Our client is a pharmaceutical company based in Canton de Neuchâtel
**Quality Control Associate Director H/F**
* Guide, mentor & develop your teams to achieve an environment of personal accountability and trust.
* Align with the site to set the strategy & priorities for your teams, ensuring we are working on the right things,
* Manage your teams by setting & tracking goals and tasks. Continuously improve processes to ensure we are doing it right.
* Ensure pro-active priority and daily activity management for team & activities (planning communication, team organization, control, checking of the defined targets),
* Ensure department processes are sufficiently defined and documented. KPIs are implement & monitored, actions are prioritized to ensure KPIs are on target.
* Communicate pro-actively, consistently, and collaboratively with peers, stakeholders, and partners.
* Use risk management & scientific assessments to ensure the depth and breadth of resource allocation (people, duration, documentation, etc. ) is commensurate to the risk, impact, and the ROI.
* Keep up to date with current industry best practices that may give an operational or strategic advantage to the company
* Accountable for the department budget (OPEX and CAPEX).
* Accountably for the on time delivery of all QC activities, to ensure overall on time delivery to the clients
* Review key department documentation, including procedures, reports, deviations, CAPAs, Change controls, etc.
* Ensure that out of specifications and deviations are appropriately investigated and resolved;
* Identify and present business cases to continuously improve, increase capabilities & capacities, to better meet client's, mitigate compliance risks, etc.
* Identify and coordinate continuous improvement & process optimizations within QC and across the site.
* Responsible for proposing solutions to client's requests, especially where there is a conflict with other department activities.
* Immediate escalation of client concerns to the project manager and site head
* Accountable for the planning, execution and tracking of all compliance activities (GxP as well as other regulatory requirements). Including:
* Accountable for the departments related topics during audits & inspections (including regulatory, compliance, client and corporate)
* Process definition, and management of documentation (SOPs, Job Descriptions, etc.), ensuring alignment to corporate policies, regulatory requirements and best practices.
* Training Curriculum definition and on-time completion of training,
* Follow up, coordination and management of CAPAs, deviations and Change Controls.
* Lead complex deviation investigations, change management, and critical quality complaint resolution activities.
Profile :
* University Degree in scientific field
* 10 years experience in a pharmaceutical company or other related GMP industry.
* Fluent in French and English
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