Quality Control Associate Director H/F
vor 2 Wochen
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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