Executive, Quality Control, Pharmaceuticals

Zentiva Poland; Ankleshwar; On-site; INR 400,000 - 600,000; Full time

Job summary

Zentiva Poland is seeking an Executive/Sr. Executive for Quality Control in Ankleshwar, India. The role involves implementing quality control activities and ensuring adherence to regulatory standards while optimizing resource utilization.

The ideal candidate should hold a Post Graduate degree in Science, have 2–5 years of experience in pharmaceuticals, and possess strong analytical and troubleshooting skills. This position plays a crucial role in maintaining product quality and compliance with HSE guidelines.

Qualifications

• 2-5 years of experience in a Pharmaceutical Company.
• Strong analytical skills necessary for quality control processes.

Responsibilities

• Perform timely analysis of raw materials and finished products.
• Maintain laboratory equipment, prepare SOPs, and manage reference standards.
• Prepare protocols for method validation and perform validation exercises.

Skills

Analytical ability

Troubleshooting

Coordination

Communication

Education

Post Graduate in Science (Organic or Analytical Chemistry)

Job description

**JOB TITLE****Executive/Sr. Executive, Quality Control, Pharmaceuticals*****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.**REQUIREMENTS****Education / Experience**Post Graduate in Science (Organic or Analytical Chemistry )2-5 years in a Pharmaceutical Company.**Technical skills &****Competencies / Language*** Analytical ability* Trouble shootings* Co ordination* Communication**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.Testing on nitrosamine and related impurities.**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/verification & transfer, cleaning validation and performing the validation exercise as per the protocol for the material and drug products.Performing analytical method validation/verification & transfer for nitrosamine and NDSRIs using LCMS/MSAnalytical method development and related troubleshooting samples on LCMS/MS.**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 LaboratoryIdentifying 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.