Imagine having the resources to influence tomorrow’s reality, today. That's Coral Drugs!
Right now, we're looking for people who think big and dream big - people a lot like you. If you are ready to discover just how far your talents can take you, we invite you to explore this site.

Coral Drugs is a professionally managed public company offering immense opportunities to learn and grow. We are dedicated to a corporate culture that inspires and rewards employees.

Our compensation and benefits packages demonstrate the high value Coral places on all our employees, both personally and professionally.

If you have an appetite for challenges, we have an exciting career for you where you will have every opportunity to progress and develop your skills.

Current Openings

Officer/Executive – Quality Assurance
• Issuance & retrieval of BPR & Testing Protocol.
• Issuance & retrieval of formats & Log books.
• Compilation of Supporting documents for Change Control/Deviation/CAPA/OOS.
• Responsible for Document Archival & up keeping.
• Preparation of Certificate of Analysis for Dispatch as per Sale order.
• To work & implement the cGMP practices in to all departments as per SOPs.
• Preparation of SOPs & relative documents.
Desirable: Minimum 01 to 03 years working experience in API post B.Sc./M.Sc./B.Pharma
Location: Murthal, Sonipat.
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Officer – Quality Control (Review of Document/Data)
• Expertise in handling the GLP section, Validation, Bulk FG, Stability Section, quality related aspects, OOS OOT, etc.
• Well versed with QC department (raw material, finish good, Validation, GLP, stability section) and department related activities and understanding of ICH & WHO guidelines.
• Sound knowledge of instruments such as HPLC (with UV, PDA RF, RI Detectors), F.T.I.R, Dissolution Tester (Electro lab), GC with Headspace, HPTLC, UV-Visible Spectrophotometer, Inductively Coupled Plasma (ICP), Atomic Absorption Spectrophotometer (AAS), TOC analyzer, Analytical Balance, Karl Fischer Apparatus and pH Meter etc.
• Possess sound analytical, interpersonal, problem solving and communication skills.
• Having good experience in API industry in Quality Control with USFDA, WHO etc. audit experience.
• Accountable for GLP section compliance/ Timely release of bulk-FG/ Validation
• Reviewing the Raw & packing materials, semi-finished and finished products and stability products reports as per different regulatory market requirement.
Desirable: 2 to 5 year must have good knowledge chemistry and hands-on experience on instrument, Literature search,Team handling, Working experience in API. Knowledge of data interpretation from NMR/IR/MASS, Analytical data review (HPLC /GC/ Stability/ Malvern/ Wet) and good documentation practice
Location: Murthal, Sonipat.
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Chemist - Quality Control
• Analysis of samples by chemical method and online reporting of in process and intermediate samples and analysis of in process validation samples.
• Analysis of samples by methods using HPLC, GC, Stability, WET, Malvern master sizer,.
• Thorough knowledge on handling & calibration of HPLC, GC, Stability, WET, Malvern.
• Knowledge on handling of OOS, Deviations, Incidents. Should have Knowledge on Wet chemistry.
• Exposure to regulatory audits. Should have the knowledge of cGMP and Good documentation practices.
• Preparation and maintenance of reagents and volumetric solutions. Should have the knowledge on instrument trouble shooting.
• Exposure to analytical method validation using HPLC, GC, Malvern and Stability.
• Shall have in-depth knowledge about the Laboratory Testing and hands on experience and troubleshooting on various Quality Control Instruments like HPLC, GC, Stability, WET, Malvern and other Laboratory instruments.
• Shall have knowledge of Method Verification / Validation and Qualification / Calibration of Laboratory Instruments.
• Shall have good investigational skills for laboratory related investigations like laboratory deviations, events, Invalid OOS etc.
Desirable: 2 to 4 year working experience API, post B.Sc./M.Sc. in Chemistry .
Location: Murthal, Sonipat.
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Officer – Quality Control (Instrumentation)
• Good Knowledge chemistry and hands-on experience on instrument.
• Literature search.
• Team handling.
• Working experience in API.
• Knowledge of data interpretation from NMR/IR/MASS.
• Analytical data review (HPLC /GC/ Stability/ Malvern/ Wet) and good documentation practice.
• Analysis of samples by chemical method and online reporting of in process and intermediate samples and analysis of in process validation samples.
• Analysis of samples by methods using HPLC, GC, Stability, WET, Malvern master sizer.
• Thorough knowledge on handling & calibration of HPLC, GC, Stability, WET, Malvern.
• Knowledge on handling of OOS, Deviations, Incidents. Should have Knowledge on Wet chemistry.
• Exposure to regulatory audits. Should have the knowledge of cGMP and Good documentation practices.
• Preparation and maintenance of reagents and volumetric solutions. Should have the knowledge on instrument trouble shooting.
• Exposure to analytical method validation using HPLC, GC, Malvern and Stability.
• Shall have in-depth knowledge about the Laboratory Testing and hands on experience and troubleshooting on various Quality Control Instruments like HPLC, GC, Stability, WET, Malvern and other Laboratory instruments.
• Shall have knowledge of Method Verification / Validation and Qualification / Calibration of Laboratory Instruments.
• Shall have good investigational skills for laboratory related investigations like laboratory deviations, events, Invalid OOS etc.
Desirable: 2 to 4 year working experience API, post B.Sc./M.Sc. in Chemistry .
Location: Murthal, Sonipat.
Apply Now
Officer-Production
• Preferable candidate from Bulk (Active Pharmaceutical Ingredients (API)
• Process handling to produce the intermediate and API finish product.
• Perform the activity of Batch to Batch Cleaning, Periodic Cleaning and change over cleaning of all equipment.
• Filling of Batch processing and control record, Equipment Cleaning record, and Product changeover cleaning record etc.
• Filling of Equipment Log book, Area cleaning record, Weighing balance record, RM & PM requisition.
• Handling and Controlling of Critical Process Parameter.
• Maintain housekeeping and Cleanliness of plant.
• Handling of process within EHS norms.
• Maintain the cGMP Compliances.
• Handling Manpower at Shop Floor.
Desirable: Minimum 01 to 02 years working experience post B.Sc./M.Sc./B.Pharma
Location: Murthal, Sonipat.
Apply Now