Senior Analytical Manager

1 day ago

Jodhpur, Rajasthan, India beBeeAnalytical Full time ₹ 1,50,00,000 - ₹ 2,00,00,000
Job Description

The ideal candidate will have the ability to handle large teams in Quality Control, including an Analytical Method Validation team. The primary responsibility for leading the LC-MS, Nasal analytical, FT-NIR analytical teams for regular testing/method validation activities. The secondary role is responsible for backup support to the Quality Control Head of Department with daily updates, monthly sample status, Lab management, training, monthly review meetings and coordination with all stakeholders to align the work as per requirements.

Main Responsibilities:

  • Primarily responsible for leading the QC-AMV team size of 30+ members (LC-MS, Nasal and FT-NIR team) for regular testing/method validation activities and with sound analytical knowledge and good leadership qualities to achieve company goals.
  • Secondary responsible for backup support to the QC HOD with daily update, commercial output, monthly sample status, Training, monthly review meeting and coordination with all stakeholders to align the work as per requirements.
  • Responsible for Execution & approval of different types of Quality Management System (OOS, OOT, Investigation etc) and identify scientific root causes with effective CAPA and maintain Lab compliance.
  • Responsible to design and execute planning of analysis (Routine work, Method validation and Method transfer), data interpretation and presenting to HOD.
  • Should be self-driven, have the capability to make self-decision and be a good learner. Providing guidance to team members for improving the work quality and monitoring and reporting on key performance indicators (KPIs).
  • Shall be responsible for leading all types of QC-AMV work in the absence of QC-HOD and actively participate in departmental improvement programs to enhance the Output and Quality.
  • Collaborating and coordinating with cross-functional teams like QA, RA, R&D and PMI to proceed the allocated task with ownership and accountability.
  • Stay updated on industry developments and emerging trends to ensure they remain competitive for LC-MS and FT-NIR techniques.
  • Responsible for adherence to Good Laboratory Practice (GLP) and Health, Safety Environment system in Laboratory and responsible for facing the FDA Audit (US, MHRA, EU) individually.

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