Executive Quality Control, Pharmaceuticals

Zentiva Poland; India; On-site; INR 400,000 - 600,000; Full time

Job summary

A pharmaceutical company located in Ankleshwar, India, is seeking an Executive for Quality Control to implement quality control activities adhering to regulatory guidelines. The ideal candidate holds a postgraduate degree in Science and has 1-5 years of experience in a testing laboratory, preferably in pharmaceuticals. Responsibilities include performing sampling and analysis, equipment calibration, and ensuring compliance with quality standards.

Qualifications

• 1 - 5 years in a chemical & instrumental testing laboratory with exposure to GMP, GLP.

Responsibilities

• Perform timely sampling and analysis of raw materials and finished goods.
• Perform calibration & maintenance of lab equipment.
• Coordinate with production and warehouse for analytical activities.

Skills

Analytical ability

Troubleshooting

Coordination

Communication

Education

Post Graduate in Science (Organic or Analytical Chemistry)

Job description

Executive Quality Control, Pharmaceuticals page is loaded## Executive Quality Control, Pharmaceuticalslocations: India / Ankleshwartime type: Full timeposted on: Posted Todayjob requisition id: R2469098**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 · CommunicationBehavioural Competencies: Accountability, Authenticity, Collaboration, Courage and Trust**Key Responsibility :**1. Testing1.1. 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.2. Good Laboratory Practice2.1. 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.3. Validation3.1. Performing the validation exercise as per the protocol. Maintaining raw data related to validation.4. Management of laboratory Consumables4.1. Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.5. Co ordination5.1. Coordinating with production, and warehouse for analytical activities.6. Other6.1. 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.