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 .

Roles and Responsibilities Ensure compliance with statutory regulations, including Factories Act, MPCB rules, and other relevant laws. Conduct regular safety audits to identify hazards and implement corrective actions. Develop and maintain an effective Environmental Management System (EMS) to minimize environmental impact. Provide training on industrial safety, risk assessment, accident investigation, and occupational health best practices. Collaborate with cross-functional teams to develop policies and procedures for EHS management. Desired Candidate Profile 4-6 years of experience in EHS management or related field. Strong knowledge of Ehs Compliance, Safety Audit, Safety Management, Industrial Safety, HSE Management, Occupational Health, Risk Assessment, Hazard Identification/Analysis. Experience with implementing ISO 45001:2018 OHSAS 18001:2007 standards.

"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: - Packing Operator - 5 Nos Interested candidates can share your updated resume to career@medopharm.com

Medopharm has been a pioneer in the field of pharma for more than 55 years in the industry. We are hiring candidates for one of our group companies for the HR Executive role. Required Experience: 1 to 3 years Location: Chennai Roles and Responsibilities: Recruitment & Onboarding: Assist with posting job openings, screening resumes, coordinating interviews, and managing the onboarding process for new faculty and staff. Employee Records & Data Management: Maintain accurate and up-to-date employee records, including personal files, contracts, and attendance data. Payroll & Benefits: Support the payroll department, assist with the administration of employee benefits, and help resolve payment-related issues. Employee Support: Respond to general employee queries, handle administrative requests, and provide day-to-day support to staff and management on various HR matters. Compliance: Assist in ensuring HR policies and procedures are followed and updated, keeping abreast of relevant employment laws. Training & Development: Help organize training sessions and support the creation of training materials under the guidance of a manager. Performance Management: Support the processes for performance reviews and help facilitate employee growth and development within the institution. Interested candidates can share your updated resume to career@medopharm.com

Medopharm has been pioneer in the field of pharma for more than 55 years in the industry. We are hiring candidates for one of our group companies for the System/ Network Administrator role . Required Experience: 5 to 8 years Location : Chennai Roles and Responsibilities System, Server maintenance and support Network, administration and troubleshooting Understanding of firewall experience with firewall configuration Windows/ Linux server maintenance VoIP/ IP telephone system support Knowledge of Google Workspace and internet technologies Handling a live-streamed event. Interested candidates can share your updated resume to career@medopharm.com

Medopharm has been pioneer in the field of pharma for more than 55 years in the industry. We are hiring candidates for one of our group companies for the CCTV Admin role . Required Experience: 5 to 8 years Location : Chennai Roles and Responsibilities CCTV installation, configuration, and maintenance IP camera systems -Matrix, Hikvision..etc Video management software (VMS) ENVR/ NVR setup and troubleshooting Network configuration for CCTV - LAN, IP add and port forwarding Remote monitoring setup -mobile apps Video storage management and retrieval Cabling and power supply -PoE, CAT 6 Knowledge of security systems -access control, alarms Interested candidates can share your updated resume to career@medopharm.com

Roles and Responsibilities 1. Responsible for implementation & monitoring of cGMP/GDP practices at site. 2. Responsible for periodic review of all quality Documents for appropriateness. 3. Preparation of SOPs and handling of QMS tools like deviation change control, CAPA. 4. Responsible for approval/rejection of deviations /change controls pertaining to corporate activities. 5. Oversee the team of technical personnel handling order processing artworks finalization BOM updating of products and follow ups. 6. Responsible for co-ordination and submission of Quality documents for regulatory submissions. 7. Responsible for maintenance, periodical update and review of technical agreements with domestic and overseas customers. 8. Coordinate the activities of plant GMP inspections/audits by regulatory authorities, MOHs and clients and support compliance response submissions and follow up on closure of audit observations. 9. Responsible for management of annual product reviews as per schedule. 10. Monitoring monthly management review meetings and report circulation of the report. 11. Monitoring/Participation in self-inspections or quality audits for effectiveness and applicability of quality system. 12. Monitoring of training program calendars in place and execution status. 13. Responsible for evaluation and investigation of product complaints received at Medopharm Private Limited. 14. Participate in investigation for field alert or product recall. 15. Coordinate with all connected departments like Regulatory, purchase, planning, Artwork, plant QA and other departments. 16. Responsible for activities related to compliance management cell at the site. 17. Responsible for tracking of CAPAs and its implementation status. 18. Responsible for tracking of regulatory commitments and it implementation status. 19. Responsible for GMP spot checking on shop floor to verify effectiveness of implemented Actions. 20. Responsible for complaint investigations. 21. Responsible to facilitate implementation of regulatory updates. 22. Responsible for performing spot challenge studies for GMP activities at the site. Desired Candidate Profile Candidate should have good communication skills and Pharmaceutical OSD Experience required