Executive Quality Control, Pharmaceuticals

Zentiva Poland; Ankleshwar; On-site; INR 600,000 - 900,000; Full time

Job summary

Zentiva Poland in Ankleshwar, India seeks an Executive Quality Control to implement QC activities in line with regulatory and global quality directives. You will perform testing on raw materials, in-process samples, and finished products, ensuring data integrity and adherence to HSE guidelines.

The role requires 1–4 years in a pharma setting and strong coordination with production and warehouse teams. The incumbent will contribute to calibration, SOP preparation, and investigation of any

Qualifications

• Testing raw materials, intermediates and finished goods for Pharmaceuticals.
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Responsibilities

• Performing analysis of raw materials, intermediates, finished products and other samples.
• Analyzing market complaints, stability, process and cleaning validation samples.
• Laboratory calibration and maintenance; assisting qualification of equipment.
• Review pharmacopeias for specifications; prepare SOPs and test formats.
• Manage reference standards, reagents, lab consumables; maintain records.
• Participate in investigations of out-of-spec results and retesting.
• Prepare analytical method validation/ cleaning validation protocols.
• Coordinate with production and warehouse for analytical activities.
• Ensure compliance with HSE requirements for QC Laboratory.
• Carry out any other assignments per Dept. Head.

Skills

Analytical ability

Troubleshooting

Coordination

Communication

Leadership

Accountability

Collaboration

Courage

Trust

Authenticity

Education

Postgraduate in Science (Organic or Analytical Chemistry)

Job description

JOB TITLEExecutive Quality Control, PharmaceuticalsREQUIREMENTSEducation / ExperiencePost Graduate in Science (Organic or Analytical Chemistry )1-4 years in a Pharmaceutical Company.Technical skills &Competencies / LanguageAnalytical abilityTrouble shootingsCo ordinationCommunicationBehavioural Competencies(LEAD and others)Accountability, Authenticity, Collaboration, Courage and TrustJOB PURPOSEGenericImplement 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 ACCOUNTABILITIESTestingPerforming 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 PracticePerforming 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.ValidationPreparing protocol for Analytical Method validation, cleaning validation and performing the validation exercise as per the protocol.Management of laboratory ConsumablesIdentifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.Co ordinationCoordinating with production, and warehouse for analytical activities.OtherCompliance 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.