Medopharm

Company Description Part of the $100 million Chordia Group, Medopharm is a leading manufacturer and exporter of pharmaceutical products in India. With 55 years of experience, Medopharm carries over 100+ domestic brands and exports generic drugs to over 160 countries across the globe. The company is known for its commitment to quality and innovation in the pharmaceutical industry. Medopharm's expertise and global reach make it a key player in the healthcare sector. Role Description This is a full-time on-site role for an Executive/Sr. Executive located in Chennai. The individual in this role will be responsible for daily management tasks, coordinating between departments, overseeing execution of projects, and ensuring compliance with company policies. Additionally, the role involves interfacing with clients, conducting market research, and contributing to business development strategies. Qualifications Management and coordination skills Experience with client interfacing and business development Proficiency in project execution and adherence to compliance Excellent communication and interpersonal skills Familiarity with market research techniques Strong problem-solving abilities Ability to work independently and as part of a team Experience in the pharmaceutical industry is a plus Bachelor's degree in Business Administration, Management, or related field Show more Show less

"Medopharm Private Limited" is a 55 year old company pioneer in the field of Pharma and We are expanding our plant and have the following openings in the Maintenance Department with experience in HVAC, plant machinery maintenance, electrical, plumbing, utility, and water plant maintenance for the Chennai, Guduvanchery location. Roles and Responsibilities Perform breakdown maintenance, electrical maintenance, HVAC maintenance, machine maintenance, mechanical maintenance, plumbing technician work, preventive maintenance, STP (Sewerage Treatment Plant) maintenance, utility maintenance, and water treatment plant maintenance. Conduct repair and maintenance activities to ensure optimal equipment performance. Troubleshoot issues with electrical systems and machinery. Collaborate with team members to resolve complex technical problems. Maintain accurate records of work performed. Desired Candidate Profile 2-7 years of experience in pharmaceutical industry or related field. Strong knowledge of electricals, mechanics, HVAC systems, and plumbing principles. Proficiency in breakdown maintenance, preventative maintenance practices. Vacancy details: - HVAC - 2 Technician Plant Machinery Maintenance - 3 Technician Utility Maintenance - 4 Technician Water Plant System - 1 Technician Interested candidates can share your updated resume to career@medopharm.com

"Medopharm Private Limited" is a 55-years-old company pioneer in the field of Pharma and We are expanding our plant and have the following openings in the Production Department with experience in Granulation, compression & Coating operator for the Chennai, Guduvanchery location. Vacancy details: - Granulation Operator 5 Nos Coating Operator - 4 Nos Compression Operator – 5 Nos Interested candidates can share your updated resume to career@medopharm.com Roles and Responsibilities Operate Granulation and blenders, FBD & RMG (Rigid Pipeline) equipment to ensure efficient production processes. Operate compression equipment to ensure efficient production processes. Operate coating equipment to ensure efficient production processes. Monitor machine performance and troubleshoot issues to minimize downtime and optimize productivity. Maintain accurate records of production data and quality control metrics. Desired Candidate Profile 2-7 years of experience in operating various Production machinery such as Granulation, RMS, FBD, blenders, compressors, coaters etc. .

Company Description Part of the $100 million Chordia Group, Medopharm is a renowned manufacturer and exporter of pharmaceutical products in India. With over 55 years of experience, Medopharm offers a wide range of over 100 domestic brands and exports generic drugs to more than 110 countries worldwide. The company prides itself on its quality manufacturing and commitment to global health. Role Description This is a full-time on-site role for a Maintenance/Engineering Technician located in Tamil Nadu, India. The Maintenance/Engineering Technician will be responsible for maintaining and repairing equipment, troubleshooting and resolving technical issues, performing routine inspections, and ensuring that all machinery and equipment comply with safety standards. The role may also include duties such as conducting preventive maintenance and collaborating with other departments to improve operational efficiency. Qualifications Technical Skills in equipment maintenance, troubleshooting, and repair Knowledge of safety standards and compliance Experience in performing routine inspections and preventive maintenance Strong problem-solving and analytical skills Ability to collaborate effectively with other departments Excellent communication skills Relevant technical certifications or a degree in Engineering or a related field Experience in the pharmaceutical industry is a plus

Role & responsibilities 1. Identification and commercialization of Contract Manufacturing Organizations as per the business needs. 2. Performing assessment for the identified CMO in co-ordination with CQA. 3. Ensuring information related to new product under consideration is arranged from the identified CMO as per agreed timelines. 4. Organizing / participating technical audits and ensure compliance to the observations and findings 5. Negotiate commercials with CMO to avail the most competitive price 6. Ensuring commercial and technical agreements are in place and renewed from time to time 7. Managing technology transfer at new CMO when possible. 8. Ensuring delivery of products from CMOs as per schedule 9. Maintaining healthy business relations with existing and new partners (CMO) 10. Establishing production systems and productivity norms at CMO 11. Performing periodical Quality audits along with QA at CMO 12. Analysing the market complaints regarding the products manufactured at CMO 13. Attending queries from authorities regarding CMO products. 14. Supporting export documentations from CMO 15. Co-ordinating with Distribution team and reviewing the FG stock position every month after stock closing and to plan production of FG as per the requirement. 16. Preparing the 3 month Rolling Plan sheet in co-ordination with Admin Marketing & distribution 17. Maintaining the Inventory of minimum as required 18. Preparing the new products costing and existing products price revision 19. Co-ordinating with CMO for forecast, costing, negotiation, order follow up and delivery 20. Attending the export enquiries related to products from CMO 21. Actively participating in new product development regards to the products from CMO. 22. Attending the clinical trials requirement and addressing to the concerned 23. Performing Packaging development whenever requires 24. Continuously learning the new developments and applying. Preferred candidate profile 10+ years of experience in relevant field. Candidates with Good communication Skills

Role & responsibilities 1. Creating Pre-Shipment invoice as per the Export sales order and Packing details /FG inventory stock details received from Warehouse. 2. Monitoring and Correcting Customer Product code, Product name, in FG master as per buyer Purchase order 3. Getting the Drawback& License details from excise dept. and prepare the export invoice, packing list, Customs declaration form and import quantity, license copy send to CHA, Warehouse team and Excise team. 4. Checking the shipping bill check list and approving the same to customs agent 5. Receiving freight bill to check the company name & GST details and freight component after entering the freight bill in speed p & upload the bill. 6. Providing invoice, packing list, BL copy to warehouse team to enable them to send the same to inspection agencies (SGS, BIVAC) 7. Filing and getting the ECTN certificate through online for west African shipments. 8. Preparing packing list for IDA format 9. Following the freight payment with account department & get the UTR No update the vendors & collet the BL. 10. Updating in Speed-p shipping bill no and date, BL number, drawback, license, discount, commission amount, port code, freight, insurance details in speed P and upload the shipping bill copy. 11. Co coordinating with CHA for export shipments and sending supporting documents (NONDG, and MSDS, Value declaration form). 12. Organise the container from Sudan shipment and coordinate to arrange COA, Drug license, TAX invoice and related document. 13. Forwarding the invoice, packing list and shipment related document to forwarder. 14. Checking the Bill of Export for SEZ export dispatches and arranges the original BOE. 15. Update in export invoice screen in drawback & license details. 16. Checking the sales order all mandatory field are filling. 17. Inform to CHA declare the shipping bill in commission, discount and which bank to file the shipping bill.

Job Description: Regulatory Affairs Executive (ROW Markets) Industry: Pharmaceuticals Experience: 3-5 Years Loaction: Chennai Key Responsibilities: Dossier Submissions: Compile & submit ACTD, CTD, and country-specific dossiers for ROW markets. Regulatory Queries: Prepare and respond to health authority queries on submitted dossiers. Document Review: Review BMR, specifications, COA, MOA, and technical documents for compliance. Artwork Coordination: Ensure accuracy in labeling & packaging artwork with regulatory standards. FDA Compliance: Maintain records for FDA licenses (Product Permission, CoPP, FSC) . Legal Documentation: Track notarized & legalized documents for international submissions. Eligibility & Requirements: Education: B.Pharm / M.Pharm (Pharmacy graduates preferred). Experience: 3-5 years in regulatory affairs, dossier submissions, or pharma compliance . Skills: Strong knowledge of ACTD/CTD dossier formats . Familiarity with FDA, EMA, and ROW market regulations . Attention to detail in documentation & compliance checks . Proficient in regulatory tracking systems & MS Office .