Hiring.Camp

Executive Quality Control, Pharmaceuticals   

Zentiva is

·

Yesterday

Location
Ankleshwar, India
Type
Full-time
Source
Workday

Description

JOB TITLE 

Executive Quality Control, Pharmaceuticals 

 

REQUIREMENTS 

 

Education / Experience 

Post Graduate in Science (Organic or Analytical Chemistry ) 

2 - 5 years in chemical & instrumental testing laboratory with exposure to GMP, GLP. 

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 sampling and 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. 

Managing reference standards, working standards, laboratory reagents & chemicals. 

Arranging and observing Control Samples and maintaining record. 

Participating in Investigation of out of specification results, performing retesting. 

Maintaining laboratory raw data related to testing activity. 

Validation 

Performing the validation exercise as per the protocol. Maintaining raw data related to validation. 

  

 

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.      

Skills

GMPCompliance

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