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
Current Openings
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- Control/Deviation/CAPA/OOS.
- Handling & Investigation of OOS.
- Preparation & Review of SOP’s.
- Handling customer Complaints.
- Handling 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
- Qualification: B.Sc./M.Sc./B. Pharma.
- Location: Murthal, Sonipat.
- Posting Date: 13/12/2022
- 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).
- Desirable: Minimum 02 to 05 years working experience with API.
- Qualification: B.Sc./M.Sc, Diploma in Chemical.
- Location: Murthal, Sonipat.
- Posting Date: 13/12/2022
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- Multistep Organic synthesis of API’s & Intermediates.
- Process Development.
- Basic knowledge of NMR.
- Good knowledge of searching literature & scientific data.
- Carryout Various Organic reactions.
- Desirable: Minimum 02 to 04 years working experience with API.
- Qualification: M.Sc. Organic Chemistry.
- Location: Murthal, Sonipat.
- Posting Date: 13/12/2022
- Preparation and review of cooperate quality policies.
- Vendor management and evaluation for effectiveness.
- Ensure effective implementation of SOPs and procedure across the site.
- Evaluation of correctness of the procedure and effectiveness.
- Preparation and review of Audit response and supporting data.
- Establish a culture of compliance and collaboration by putting Quality processes in place.
- Provide guidance for investigation as well as CAPA plan for compliance issues and observations.
- Ensure effective implementation of CAPA.
- Development of effective training programme for GXP (GMP, GDP,GLP) related procedure , practices and systems.
- Risk mitigation strategy and planning.
- Ensure all time readiness of site for audit and regulatory inspections.
- Ensure Management quality review programme in-place.
- Well versed with current regulations GMP and agency requirements.
- Desirable: Minimum 05 to 08 years working experience in API.
- Qualification: M.Sc./B. Pharma
- Location: Gurgaon/Gurugram.
- Posting Date: 13/12/2022
- Excellent verbal and written communication.
- Emailing/handle reception calls.
- Able to handle daily admin work/tasks.
- Good command in Excel & word.
- Arrange meetings.
- Attend visitors.
- Handle dispatches of couriers and parcels.
- Maintain record in system
- Maintain daily attendance in system.
- Coordinates with all departments.
- Desirable: Minimum 02 to 05 years working experience.
- Qualification: Graduation
- Location: Gurgaon/Gurugram.
- Posting Date: 29/10/2022
- 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
