Zentiva Group Hiring For Quality Control Department
.png "Zentiva Group Hiring For Quality Control Department") |
Zentiva Group Hiring For Quality Control Department |
Zentiva Group Job Vacancy Details:
Position Title: Officer / Executive – QC, Pharmaceuticals
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.
Location : Ankleshwar
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.
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
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.
What makes this position unique?This position will provide good exposure to work in GMP/ GLP environment.
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