Senior Operations Manager

1 week ago

Mangalore, Karnataka, India beBeeLeadership Full time ₹ 1,80,00,000 - ₹ 2,25,00,000
Job Overview

The Assistant General Manager is responsible for overseeing large teams of 30+ members in Quality Control (QC), including the Analytical Method Validation (AMV) team.

This role involves leading the LC-MS, Nasal analytical, and FT-NIR analytical teams for regular testing/method validation activities, as well as supporting the QC-HOD with daily updates, monthly sample status, lab management, training, and monthly review meetings.

Key Responsibilities
  • Lead the QC-AMV team (LC-MS, Nasal, and FT-NIR) for regular testing/method validation activities.
  • Support the QC-HOD with daily updates, commercial output, monthly sample status, training, and monthly review meetings.
  • Execute and approve different types of Quality Management Systems (QMS), identify scientific root causes with effective Corrective Actions and Preventative Actions (CAPA).
  • Design and execute planning of analysis (routine work, method validation, and method transfer), data interpretation, and presentation to HOD.
  • Provide guidance to team members for improving work quality and monitoring/reporting on key performance indicators (KPIs).
  • Lead all types of QC-AMV work in the absence of QC-HOD and actively participate in departmental improvement programs to enhance output and quality.
  • Collaborate and coordinate with cross-functional teams (QA, RA, R&D, and PMI) to proceed with allocated tasks with ownership and accountability.
  • Stay updated on industry developments and emerging trends to ensure competitiveness for LC-MS and FT-NIR techniques.
Required Skills & Qualifications
  • Master's degree in Science or Bachelor's/Master's in Pharmaceutical sciences.
  • Strong analytical knowledge and expertise in modern analytical instruments (HPLC, GC, LC-MS, NIR, Nasal performance testing, etc.).
  • Mix work experience in QC, AMV, and AD departments.
  • Strong leadership skills with proven ability to motivate and develop team members.
  • Exceptional problem-solving skills and strategic mindset. Solid organisational and time management skills.
  • Knowledge of Chromeleon 7.2 and Sciex software an added advantage.
  • Good working experience in Good Manufacturing Practice (GMP) and USFDA/EU Audit faced.
  • Able to achieve deliverable tasks with minimum support for analysis.
  • Excellent written and verbal communication skills.

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