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Executive Quality Control, Pharmaceuticals

Zentiva
Ankleshwar, IND
Full-time
Junior · 1–4 years experience
Onsite
Discovered 3 weeks ago

Full Job Posting

Technical skills &

  • Competencies / Language
  • Analytical ability
  • Trouble shootings
  • Co ordination
  • Communication
  • Behavioural Competencies
  • (LEAD and others)
  • Accountability, Authenticity, Collaboration, Courage and Trust
  • JOB PURPOSE
  • Generic
  • 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.
  • 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.

Qualifications

  • Education / Experience
  • Post Graduate in Science (Organic or Analytical Chemistry )
  • 1-4 years in a Pharmaceutical Company.
  • Technical skills &
  • Competencies / Language
  • Analytical ability
  • Trouble shootings
  • Co ordination
  • Communication
  • Behavioural Competencies
  • (LEAD and others)
  • Accountability, Authenticity, Collaboration, Courage and Trust
  • JOB PURPOSE
  • Generic
  • 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.
  • 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.

Responsibilities

  • Generic
  • 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.

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