Executive - Quality Control, Pharma

Zentiva; Ankleshwar; On-site; INR 400,000 - 800,000; Full time

Job summary

A leading pharmaceutical company in Ankleshwar is seeking an Executive in Quality Control to implement quality control activities and ensure compliance with regulatory directives. The ideal candidate will have a Master's in Chemistry and 1-5 years of experience. Key responsibilities include performing analyses, managing laboratory consumables, and coordinating with production. This role offers an opportunity to contribute to maintaining high standards in product quality.

Qualifications

• 1-5 years of experience in a Pharmaceutical Company.

Responsibilities

• Implement quality control activities for Pharmaceuticals.
• Perform timely analysis of raw materials and finished goods.
• Participate in Investigation of out of specification results.

Skills

Analytical ability

Trouble shootings

Coordination

Communication

Education

Master in Chemistry

Job description

JOB TITLE

Executive Quality Control, Pharmaceuticals

Site / Unit: Pharmaceuticals Ankleshwar

Department : Quality Control

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.

Key Accountabilities

Testing

• Performing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.
• Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.

Good Laboratory Practice

• Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
• Reviewing pharmacopeias for specification preparation.
• Preparing SOPs and Formats and Analytical Test Record.
• Managing reference standards, working standards, laboratory reagents & chemicals.
• Arranging and observing Control Samples and maintaining record.
• Participating in Investigation of out of specification results, retesting and review the analysis records.
• Maintaining & reviewing laboratory raw data related to testing activity.

Validation

• Preparing protocol for Analytical Method validation, cleaning validation and performing the validation exercise as per the protocol.

Management of laboratory Consumables

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

Co ordination

• Coordinating with production, and warehouse for analytical activities.

Other

• Compliance to HSE Requirements for QC Laboratory.
• Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.
• Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.

Requirements

Education / Experience

• Master in Chemistry
• 1-5 years in a Pharmaceutical Company.

Technical Skills & Competencies / Language

• Analytical ability.
• Trouble shootings.
• Co ordination.
• Communication.

Behavioural Competencies

• Accountability, Authenticity, Collaboration, Courage and Trust.