Analyst Jr. Group Leader - Bioanalytical Research

Veeda CR; Ahmedabad District; On-site; INR 1,000,000 - 2,000,000; Full time

Job summary

Veeda CR in Ahmedabad is seeking an experienced analytical scientist to lead the team in GL absence, design experiments, and coordinate resources for bioanalytical development. The role emphasizes LC-MS calibration and strict adherence to GxP guidelines.

You will develop methods, document SOPs, train staff, and ensure timely trials. The position involves handling diverse matrices and presenting findings with strong problem-solving leadership.

Qualifications

• Leadership and team coordination
• Strong problem-solving abilities in analytical chemistry
• Knowledge of GxP and regulatory requirements
• Development and validation of analytical methods
• Experience with LC-MS and related techniques

Responsibilities

• Lead the team with GL or in absence of GL
• Design experiments for development
• Resource planning and shift/manpower coordination
• Handle specialized bioanalytical techniques (peptide, liposomal methods)
• Manage endogenously present molecule work and rare matrices
• Ensure LC and LC-MS calibration and perform analyses via LC-MS with GxP
• Prepare Method SOPs and validation protocols
• Coordinate with SGL, QC, RW and QA for audits and inquiries
• Train fresh analysts and lead team development
• Drive target achievement and effective work pressure management
• Oversee equipment optimization (MS/Chromatography) and method parameterization

Skills

Leadership

People management

Problem solving

Quality compliance

Analytical technique development

Tools

LC

LC-MS

Mass spectrometry

Chromatography

Job description

Role & responsibilities

Perform Analysis :

• Lead the team along with GL or in absence of GL
• Design the experiment for development
• Resource planning skills and shift and manpower planning and coordination
• Special bioanalytical techniques- Peptide, Liposomal method handling
• Endogenously present molecule handling and Approach
• Rare matrix (Aqueous Humour, Skin, tissue etc)handling conceptual clarity
• failure handling and resolution skills
• coordinate with SGL for targets alignment and execution
• target achievement as team
• LC and LC/MS- calibration
• Perform analysis via LCMS. Follow GxP
• Work pressure effective handling skills

Documentation and compliance :

• Preparation of Method SOP, Method validation protocol and Bioanalytical study plan
• Awareness of various sponsor and regulatory requirement for protocol preparation
• coordination with SGL, QC, RW and QA for response to query and observation
• the regulatory and sponsor communication during audit
• Supervise and verify online documentation of development trial in Method Book (Laboratory Record Book), validation experiment documentations, entry in log books in control forms as per SOP, evaluate experiment out-come with pre-defined validation/Study protocol
• Document all linked activities and forms as per SOP.

Research & Development :

• Literature review i.e. published pharmacopeia guidelines/research documents received from GL and SGL.
• Optimize the equipment (Mass Spectrometer) & Chromatography parameters (Analytical Column) for specific analyte (Drug sample), perform extraction trials by using blank matrix and finalize method for validation.
• Validation: Perform experiments as per protocol
• Presentation and publication opportunity
• preparation of New SOPs and processes special techniques - Micro capillary, SFC, ICP-OES handling

Equipment Calibration :

• LC and LC/MS- calibration
• Train analyst for various calibration activity and verify the calibration record documented by analyst

Training:

• To coordinate assist/support in on-the-job trainings for fresher
• Training of team
• Presentation and publication opportunity

Professional skills :

• Problem Solving Skills
• Leadership
• People Management