
Leadership Team Manager
2 weeks ago
The role of a Leadership Team Manager is to lead large teams in Quality Control, including the Analytical Methods Validation team. The primary responsibility is for leading the LC-MS, Nasal analytical, and FT-NIR analytical teams for regular testing/method validation activities.
Main Responsibilities:- Lead the QC-AMV team size of 30+ members (LC-MS, Nasal, and FT-NIR team) for regular testing/method validation activities with sound analytical knowledge and good leadership qualities to achieve business goals.
- Support the Head of Department with daily updates, commercial output, monthly sample status, training, monthly review meetings, and coordination with all stakeholders to align work as per requirements.
- Execute and approve different types of QMS (OOS, OOT, Investigation, etc.) and identify scientific root causes with effective CAPA and maintain Laboratory compliance.
- Design and execute planning of analysis (routine work, method validation, and method transfer), data interpretation, and present to the Head of Department.
- Making informed decisions, being a good learner, and providing guidance to team members for improving work quality and monitoring key performance indicators (KPIs).
- Lead all types of QC-AMV work in the absence of the Head of Department 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.
- Stay updated on industry developments and emerging trends to remain competitive for LC-MS and FT-NIR techniques.
- Adhere to GLP and Health, Safety Environment system in the Laboratory and face FDA Audit (US, MHRA, EU) individually.
- A Master's Degree in Science or a Bachelor's or Master's degree in Pharma.
- Strong analytical knowledge and expertise in modern analytical instruments (like HPLC, GC, LC-MS, or NIR or Nasal performance testing, etc.) with the ability to interpret complex data and generate insights.
- Preferring 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, with the ability to manage multiple projects and deadlines.
- Knowledge of Chromeleon 7.2 and Sciex software will be an added advantage.
- Good working experience in GMP and USFDA/EU Audit faced.
- Able to achieve deliverable tasks with minimum support for analysis.
- Excellent written and verbal communication skills, with the ability to present findings clearly and effectively.
This role requires managing work in all shifts and may require travel to other sites if needed.
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