Executive Quality Control, Pharmaceuticals

Zentiva • Pharmaceuticals • 7 hours ago
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Salary
≈ $29k – $80k per year (Estimated)
Location
In office (India)
Employment
Full-Time
Overview
Company
Impact
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Zentiva

Zentiva is a prominent European pharmaceutical enterprise specializing in the production and supply of high-quality generic medicines and consumer healthcare products. Headquartered in Prague, Czech Republic, the company operates across dozens of international markets, delivering accessible treatments to millions of patients. Managing the complete lifecycle from laboratory research and manufacturing to global distribution, it focuses on expanding access to affordable, essential medications.
zentiva.lv • HQ: Prague, Czech Republic • 501-1000 employees

JOB TITLE

ExecutiveQuality Control, Pharmaceuticals

REQUIREMENTS

Education / Experience

Post Graduate in Science (Organic or Analytical Chemistry )

1-4years in a Pharmaceutical Company.

Technical skills &

Competencies / Language

  • Analytical ability

  • Trouble shootings

  • Co ordination

  • Communication

BehaviouralCompetencies

(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 & maintenanceof 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 Investigationofout 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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