Executive Quality Control Pharmaceuticals

JOB TITLE : Executive Quality Control, Pharmaceuticals

JOB PURPOSE: Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.

Education / Experience: Post Graduate in Science (Organic or Analytical Chemistry) 1 - 5 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.

Preferably from Pharma background only.

Technical skills & Competencies / Language

• Analytical ability
• Trouble shootings
• Co ordination
• Communication
  
  

Behavioural Competencies: Accountability, Authenticity, Collaboration, Courage and Trust

Key Responsibility

• Testing
  
  

1.1. Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.

1.2. Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.

• Good Laboratory Practice
  
  

2.1. Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.

2.2. Managing reference standards, working standards, laboratory reagents & chemicals.

2.3. Arranging and observing Control Samples and maintaining record.

2.4. Participating in Investigation of out of specification results, performing retesting.

2.5. Maintaining laboratory raw data related to testing activity.

• Validation
  
  

3.1. Performing the validation exercise as per the protocol. Maintaining raw data related to validation.

• Management of laboratory Consumables
  
  

4.1. Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.

• Co ordination
  
  

5.1. Coordinating with production, and warehouse for analytical activities.

• Other
  
  

6.1. Compliance to HSE Requirements for QC laboratory.

6.2. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.

6.3. Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.

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