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

Manager – Purchase
• Receive indents from users.
• Arrange offers from suppliers make comparatives and handed over to HOD for Receive indents from users.
• Arrange offers from suppliers make comparatives and handed over to HOD for evaluation.
• PO sent to vendors.
• Follow up to vendors for timely deliveries.
• Searching new vendors on cost & quality & presenting to the HOD for approval.
• Maintain good relationships between users & vendors.
• Management of safe goods receipt in coordination with the concerned departments.
• Follow up with Transporters / Couriers for delivery of material.
• Be an active part for organization development activities.
• Providing inputs and essential data for budgeting to the HOD/management.
Desirable: Minimum 5 years working experience post B.Sc./B. Com/B. A/ M.B. A- Material management / procurement.
Location: Murthal, Sonipat.
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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- Production
• 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.
Desirable: 1 to 3 year working experience in API.
Location: Murthal, Sonipat.
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Officer - R&D
• Literature Search of the product.
• Column Chromatography/ Crystallization of the compound/HPLC.
• Identification of synthetic route.
• Synthetic organic chemistry.
• Process of raw materials and chemicals required for final synthetic route.
• Conduct exploratory experiments to finalize the synthetic route.
• Provide complete technical details to Analytical Development Department to develop the analytical method.
• To analyze the data related to process / analytical results.
• Characterization of molecules by NMR/MASS/IR/TLC/MS
Desirable: 2 to 3 year working experience.
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 rich 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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Officer – Quality Control (Wet lab/Stability)
• 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 (Wet Lab) and good documentation practice.
• Knowledge of GMP standards.
• Knowledge of instrument handling.
• Having experience in Wet Lab/stability.
• Knowledge of GLP compliances in QC lab.
Desirable: 1 to 2 year working experience post B.Sc./M.Sc. in Chemistry .
Location: Murthal, Sonipat.
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Coordinator – Sales & Marketing
• Identify customer’s requirement of quality for existing and new products.
• Communicate with clients regarding possible orders, existing orders etc.
• Correspond with quality control regarding material specifications or organizing samples, special reports, etc.
• Conduct contract review on receipt of order and send order acceptance. Facilitate preparation of export documents.
• Maintaining all correspondence of the marketing department.
• Assisting the CEO and chief operating officer in their promotional activities.
• Assignment of codes for incoming and outgoing product samples.
• Update procedures of the department.
Desirable: 3 to 5 year working experience.
Location: Murthal, Sonipat.
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Sr. Executive : Regulatory Affair
• Prepare and review regulatory submission for regulated, Semi regulated and row markets.
• Drafting and Compilation of documents for preparation of dossiers and handling related queries.
• Hands on experience of CTD, ACTD and country specific dossiers.
• Responding to queries within scheduled timelines.
• Co-ordination and follow ups with all functional departments.
• Review of pharmaceuticals Development Report (PDR), Manufacturing and validation documents, (QSD) Quality Standard Documents, (COA) Certificate of Analysis.
• Experienced in API Drug Master file creation and filings in regulatory and non-regulatory markets.
Desirable: 3 to 5 year working experience post M.Sc./B.Pharm/M. Pharm .
Location: Murthal, Sonipat.
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