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Zentiva

Executive - Quality Control

Posted 6 Days Ago
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2 Locations
Junior
2 Locations
Junior
The Executive - Quality Control is responsible for implementing quality control activities in pharmaceuticals, conducting analysis of materials and products, maintaining laboratory standards, and ensuring adherence to GMP and GLP guidelines. They will manage laboratory consumables and coordinate with production and warehouse for analytical activities.
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Position Title: Executive – Quality Control, Pharmaceuticals  

Job overview:

  • Implement quality control activities 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.

Responsibilities:                                                  

  • Analysis:

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

Performing analysis of Stability, process validation samples, Cleaning Validation.

  • Good Laboratory Practice

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

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.

  • Other

Coordinating with production, and warehouse for analytical activities

Compliance to HSE Requirements for QC laboratory.

Identifying and correcting unsafe conditions or behaviours 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 & Qualifications:

  • M.sc (Organic / Analytical Chemistry) / B. Pharm with 2-5 years of Experience as an analyst in similar industry
  • GMP & GLP knowledge
  • Good coordination & communication skills.  

What makes this position unique?

  • This position will provide good exposure to work in GMP/ GLP environment.

Location Information: Ankleshwar GIDC District: Bharuch State: Gujarat.

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