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Quality Control Associate Director H/F in Neuchâtel, Neuchâtel | LHH

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Quality Control Associate Director H/F

Neuchâtel, Neuchâtel

Festanstellung

Life Sciences


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

#boost

RefJN-062024-605738

Quality Control Associate Director H/F

LHH

vor 4 Tagen

Festanstellung

Life Sciences

Neuchâtel, Neuchâtel


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

#boost

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