Lead Senior Quality Professional

4 days ago

Vellore, Tamil Nadu, India beBeeQualityManager Full time ₹ 10,00,000 - ₹ 17,00,000

Job Overview

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We are seeking an experienced Senior Quality Manager to lead our QC team and drive quality excellence across the organization. The role requires strong analytical knowledge, leadership skills, and the ability to motivate and develop team members.

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About the Role

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  • Lead the QC team in regular testing/method validation activities with sound analytical knowledge and leadership qualities.
  • Provide back-up support to the HOD with daily updates, commercial output, monthly sample status, training, and coordination with all stakeholders.
  • Execute and approve different types of QMS (OOS, OOT, Investigation etc), identify scientific root causes with effective CAPA, and maintain Lab compliance.
  • Design and execute analysis planning, data interpretation, and presentation to HOD.
  • Be self-driven, make self-decision, and be a good learner, providing guidance to team members for improving work quality and monitoring/reporting KPIs.
  • Lead all types of QC work in the absence of HOD and participate in departmental improvement programs to enhance Output and Quality.
  • Collaborate and coordinate with cross-functional teams like QA, RA, R&D, and PMI to proceed allocated tasks with ownership and accountability.
  • Maintain adherence to GLP and Health, Safety Environment system in Laboratory and face FDA Audit (US, MHRA, EU) individually.
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Required Skills and Qualifications

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  • Maste degree of Science / Bachelors or Master Pharma.
  • Strong analytical knowledge and expertise in modern analytical instruments (HPLC, GC, LC-MS or NIR or Nasal performance testing etc).
  • Preferably 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 will be an added advantage.
  • Good working experience in GMP and USFDA/EU Audit faced.
  • Ability to achieve deliverable tasks with minimum support for analysis.
  • Excellent written and verbal communication skills, presenting findings clearly and effectively.
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Benefits

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  • Opportunity to work in a dynamic environment with a talented team.
  • Professional growth and development opportunities.
  • A competitive salary and benefits package.
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Others

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  • Work may require managing shifts, travelling to other sites as per company policy.
  • Responsible for ensuring compliance with GLP, Health, Safety and Environment requirements.
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