[contact-form-7 404 "Not Found"]
Careers

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

career
Current Openings

  • Knowledge of Material & finalization as per requirement.
  • Knowledge of Procurement of Lab Chemical, Lab Instrument, Raw material of API’s.
  • Preparation of quote comparison documents for management approval.
  • Follow up with suppliers for delivery of open orders.
  • Preparation and processing of requisitions and purchase orders.
  • Preparation of requests for quotation.
  • Purchase order processing.
  • Preparation of MIS, Cost Comparison Sheet and savings
  • Ensuring timely material supply.
  • Vendor payment processing.
  • Co-Ordination with Corporate Office.
  • Cost saving, delivery of material on time.
  • Desirable: Minimum 05 to 10 years working experience with Pharmaceuticals post Graduation (any specialization).
  • Location: Gurgaon/Gurugram.
  • Posting Date: 29/10/2022

Apply Now

  • 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 03 to 08 years working experience in API post B.Sc./M.Sc./B.Pharma
  • Location: Murthal, Sonipat.
  • Posting Date: 11/09/2021

Apply Now

  • 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.
  • Thorough knowledge on handling validation & calibration of HPLC.
  • 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.
  • Desirable: Minimum 04 to 10 year working experience API, post B.Sc./M.Sc. in Chemistry.
  • Location: Murthal, Sonipat.
  • Posting Date: 11/09/2021

Apply Now

  • Reviewing analytical reports as Process Validation, Finished Products RM,PM, In-Process, Stability & Control Sample stages.
  • Review the all testing protocol related to chemicals analysis.
  • Review any deviations, lab errors and out of specifications results as per established processes in line with cGMP and accordingly take appropriate actions.
  • 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.
  • Desirable: 5 to 12 year working experience API, post B.Sc./M.Sc. in Chemistry, B.Pharma/ M.Pharma
  • Location: Murthal, Sonipat.
  • Posting Date: 11/09/2021

Apply Now

  • 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.
  • Equipment Handling Reactors (SS, GLR).
  • Maintain departmentally document as per GMP.
  • Maintain departmentally document as per GMP.
  • Record and report test results to supervisor.
  • Daily production reporting to plant manager.
  • Maintaining BMR, Clean room document & in process check record.
  • Involved in process improvement at intermediate stages.
  • Maintain housekeeping and cleanliness of plant.
  • Handling of process within EHS norms.
  • Maintain the cGMP compliances.
  • Desirable: Minimum 04 to 10 years working experience post B.Sc./M.Sc./B.Pharma
  • Location: Murthal, Sonipat.
  • Posting Date: 11/09/2021

Apply Now

  • Compilation, preparation, and review of DMFs for US, Europe, Canada and ROW markets in specified eCTD or NeeS or CTD formats.
  • Setting specifications of API process development, knowledge of litigation related to Drugs and Cosmetics Act.
  • Filing annual updates and amendments to various regions of submitted DMFs.
  • Handling queries obtained from different regulatory agencies and customers.
  • Compilation, preparation and review of Technical Package of API’s.
  • Compliance to audits of regulatory bodies especially USFDA and EU.
  • Generation of documents from R&D, Production, QC and QA of newly developed API’s.
  • Responsible for record keeping and to ensure correctness of records pertaining to department.
  • Responsible for all type of computer work and follow-ups.
  • Carrying out the initial assessment of Vendor Questionnaire and relevant documents.
  • Maintain housekeeping and cleanliness of plant.
  • To impart scheduled trainings of ICH guidelines pertaining to department.
  • Desirable: Minimum 03 to 05 years working experience B. Pharma/M. Pharma
  • Location: Murthal, Sonipat.
  • Posting Date: 11/09/2021

Apply Now