Role & responsibilities Production 1. To monitor all production activities of production department. 2. To plan department production schedules according to marketing requirement. 3. To co-ordinate with Plant Head and Stores-In-Charge for procurement of raw and packing materials required for production. 4. To approve all raw/packing material indents for batch manufacturing of products. 5. To plan monthly production schedules and make necessary changes in day to day schedules whenever required 6. Ensure optimal usage of manpower for carrying out different activities in the department. 7. To co-ordinate with maintenance department regarding the utilities requirement and its performance. 8. To co-ordinate with Q.C. department for approval of Raw Materials/Semi Finished/Finished products. 9. To co-ordinate with Q.A. in preparation of MMR's, BMR's/ BPRs and SOP's. 10. To co-ordinate with concerned agencies for validation of critical areas and equipment. 11. To co-ordinate with Q.A. for validation of equipment and preparation of SOPs. 12. To follow cGMP in all areas of production. 13. To co-ordinate with product development during processing of new products. 14. To ensure that all BMR's and other production documents are maintained as per requirement. 15. To maintain discipline in the production areas. 16. To ensure safety of workers and other staff in departments. 17. To ensure that manufacturing and other operations are carried out as per the laid down procedures in MMR's and SOP's. 18. To co-ordinate with maintenance department for general preventive maintenance and breakdown maintenance. 19. To appraise Plant Head /Management regarding day-to-day production activities. 20. To train and arrange training for personnel. 21. To ensure hygiene in all areas of production and hygiene of personnel in the department. 22. To delegate responsibilities to subordinates whenever required. 23. To ensure that proper batch yields are obtained. 24. To indent for consumables and miscellaneous items required for production. 25. To carry out any other duties assigned by Plant Head. 26. Responsible for the day - today production planning. 27. Work assignment to production executives as per production planning. 28. Monitoring the GMP documents like equipment logbooks/sheet, records of daily activity, housekeeping etc. 29. Online filling of BMR, BPR of the batches and review of the same. 30. Preparation of Monthly report, production planning and Implementation, Yield improvement, Optimum Capacity Utilization, Productivity Improvement, Reduction of Wastage. 31. Periodic audit of all the activities / operation of the plant ensure statutory compliance / In-house standard compliance. 32. Submitting consolidated monthly report on all aspects of Plant operations to the Administrative Director. Preferred candidate profile only Candidates with Pharma experience are requested to apply. Perks and benefits Commensurate with experience and performance track record-will not be a constraint for the right candidate.only
Role & responsibilities - QA (IPQA & AQA) 1. Personal Hygiene check-up of the staff and employees 2. Maintaining Quality Aspects and issuing Line clearance in Production department. 3. Controlling Document flow and completion of BMR and BPR in both the above areas 4. Checking Log books for the machineries in the above said areas 5. Issue and Receiving of Stereos/Computer generated OPD for packing 6. Ensuring In process controls as per Procedure. 7. Ensuring process is validated and carried out as per batch record instructions. 8. Ensuring process is validated and carried out as per batch record instructions. 9. Ensuring status labels/labeling of containers, equipments and materials. 10. Ensuring online documentation and timely entries of all operations/activities. 11. To monitor and ensure physical parameters such as Temperature, RH & Differential pressure. 12. Monitoring of personnel movement and clean room behaviour in process area. 13. Collection of stability and control samples 14. Collection of Finished product samples 15. Machine parameter verification 16. Verification of loads as per validated load pattern in Autoclave 17. Any other assignment given by the Quality assurance manager from time to time. only Candidates with Pharma experience/ Immediate or within 30 days joiners are requested to apply. Perks and benefits As per company standard
QA( AQA) To review the Audit Trial Report Review of SOPs pertaining to Quality Control (Chemical & Microbiology) Review of Stability protocols & Report Responsible for investigation and closure of OOL, OOT & OOS. To review the Equipment & usage log books of QC& microbiology. To review the calibration of QC & microbiology equipments Follow up for the closure of deviations/ change controls/CAPAs pertaining to QC area. To log OOS, OOT and OOLs and update the relevant databases and logbooks To Review the analytical method validation/other study Protocols, ROA and Reports Verification of Media Fill vials. Review of EMP, Water trends, specifications and testing Review of STPs & GTP materials/ Product. To prepare, review of the Quality Risk assessment documents To prepare, review of the Annual Product Quality Review (APQR) To review the Record of analysis pertaining to RM, PM, In process, validation samples and FP To review the RM, PM Sampling and it approval. only Candidates with Pharma experience/ Immediate or within 30 days joiners are requested to apply. Perks and benefits As per company standard
Role & responsibilities Production 1. To monitor all production activities of production department. 2. To plan department production schedules according to marketing requirement. 3. To co-ordinate with Plant Head and Stores-In-Charge for procurement of raw and packing materials required for production. 4. To approve all raw/packing material indents for batch manufacturing of products. 5. To plan monthly production schedules and make necessary changes in day to day schedules whenever required 6. Ensure optimal usage of manpower for carrying out different activities in the department. 7. To co-ordinate with maintenance department regarding the utilities requirement and its performance. 8. To co-ordinate with Q.C. department for approval of Raw Materials/Semi Finished/Finished products. 9. To co-ordinate with Q.A. in preparation of MMR's, BMR's/ BPRs and SOP's. 10. To co-ordinate with concerned agencies for validation of critical areas and equipment. 11. To co-ordinate with Q.A. for validation of equipment and preparation of SOPs. 12. To follow cGMP in all areas of production. 13. To co-ordinate with product development during processing of new products. 14. To ensure that all BMR's and other production documents are maintained as per requirement. 15. To maintain discipline in the production areas. 16. To ensure safety of workers and other staff in departments. 17. To ensure that manufacturing and other operations are carried out as per the laid down procedures in MMR's and SOP's. 18. To co-ordinate with maintenance department for general preventive maintenance and breakdown maintenance. 19. To appraise Plant Head /Management regarding day-to-day production activities. 20. To train and arrange training for personnel. 21. To ensure hygiene in all areas of production and hygiene of personnel in the department. 22. To delegate responsibilities to subordinates whenever required. 23. To ensure that proper batch yields are obtained. 24. To indent for consumables and miscellaneous items required for production. 25. To carry out any other duties assigned by Plant Head. 26. Responsible for the day - today production planning. 27. Work assignment to production executives as per production planning. 28. Monitoring the GMP documents like equipment logbooks/sheet, records of daily activity, housekeeping etc. 29. Online filling of BMR, BPR of the batches and review of the same. 30. Preparation of Monthly report, production planning and Implementation, Yield improvement, Optimum Capacity Utilization, Productivity Improvement, Reduction of Wastage. 31. Periodic audit of all the activities / operation of the plant ensure statutory compliance / In-house standard compliance. 32. Submitting consolidated monthly report on all aspects of Plant operations to the Administrative Director. Preferred candidate profile only Candidates with Pharma experience are requested to apply. Perks and benefits Commensurate with experience and performance track record-will not be a constraint for the right candidate.only
Key Responsibilities Sales & Target Achievement : Develop and execute sales strategies to meet and exceed sales targets for pharmaceutical products in the assigned area. Customer Relationship Management : Build and maintain strong, long-term relationships with doctors, hospitals, pharmacies, and other key stakeholders. Market Analysis : Analyze market trends, identify new business opportunities, and understand customer needs within the territory. Sales Operations : Plan and forecast monthly sales, manage sales budgets, and report sales figures and performance to senior management. Internal Collaboration : Liaise with marketing, product development, and regulatory teams to align sales strategies with overall company objectives. Required Skills and Qualifications • Communication : Excellent verbal and written communication skills for interacting with internal teams and external clients. • Industry Knowledge : Knowledge of the pharmaceutical industry, its products, and regulatory standards is essential. Preferred candidate profile only Candidates with Pharma experience/ Immediate or within 30 days joiners are requested to apply. Perks and benefits As per company standard
1. Product Promotion: Promote and sell pharmaceutical products to healthcare professionals. 2. Client Relationship Management: Build and maintain relationships with doctors, hospitals, pharmacies, and other healthcare stakeholders. 3. Product Knowledge: Stay updated on product information, features, and benefits to communicate with healthcare professionals effectively. 4. Sales Targets: Meet sales targets and contribute to business growth. 5. Market Insights: Gather market information, competitor activity, and customer feedback. 6. Product Training: Conduct product training and demos for healthcare professionals. 7. Territory Management: Manage territory effectively, plan sales strategies, and optimise time.Role & responsibilities Preferred candidate profile
1. Sales and Marketing of our Small volume and Large volume parantels & Tablets & capsules & Sy and pharma products within Karnataka. 2. Visit Hospitals, customers and build and maintain relationships with doctors, hospitals, pharmacies, and other healthcare stakeholders. 3. Product Knowledge: Stay updated on product information, features, and benefits to communicate with healthcare professionals effectively. 4. Market Insights: Gather market information, competitor activity, and customer feedback. 6. Product Training will be given from time to time 7. Medical representatives/Marketing executives with 1-4 years may apply Male candidates only need to apply Salary 20000,30000/- per month. Preferred candidate profile
QA( AQA) & (IPQA) **Responsibilities:** - Review the Audit Trail Report and SOPs related to Quality Control (Chemical & Microbiology). - Review Stability Protocols and Reports. - Investigate and resolve Out-of-Limits (OOL), Out-of-Trend (OOT), and Out-of-Specification (OOS) occurrences. - Review equipment and usage logbooks for QC and microbiology. - Review the calibration records for QC and microbiology equipment. - Follow up on the closure of deviations, change controls, and CAPAs in the QC area. - Log OOS, OOT, and OOL occurrences and update the relevant databases and logbooks. - Review analytical method validation, study protocols, Records of Analysis (ROA), and reports. - Verify Media Fill vials. - Review Environmental Monitoring Plan (EMP), water trends, specifications, and testing results. - Review Standard Test Procedures (STPs) and Good Trading Practice (GTP) materials/products. - Prepare and review Quality Risk Assessment documents. - Prepare and review the Annual Product Quality Review (APQR). - Review the Record of Analysis for raw materials (RM), packaging materials (PM), in-process samples, validation samples, and finished products (FP). - Review RM and PM sampling plans and approvals. **Qualifications:** - Only candidates with pharmaceutical experience and those available to join immediately or within 30 days should apply. **Additional Responsibilities:** - Lead and supervise In-Process Quality Assurance (IPQA) activities on the manufacturing and packaging shop floor. - Ensure strict adherence to current Good Manufacturing Practices (GMP) and real-time documentation. - Perform line clearance and stage-wise verification of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR). - Evaluate critical process parameters and support continuous process verification. - Handle and review deviations, CAPAs, and change controls related to in-process operations. - Conduct internal audits and assist during regulatory inspections (e.g., CDSCO, WHO). - Monitor cleanroom behavior, gowning practices, and environmental conditions. - Ensure timely review and closure of quality events. - Train junior QA and production staff on SOPs and updated regulations. - Review analytical raw data for compliance with cGMP, GLP, and regulatory standards. - Supervise analytical documentation, including method validations, instrument qualifications, and stability reports. - Perform and lead audit trail reviews for chromatographic software (HPLC/GC). - Oversee the data integrity program and ensure adherence to ALCOA+ principles. - Manage and coordinate the investigation of laboratory incidents such as OOS and OOT, providing QA oversight during investigations. - Collaborate with QC and Regulatory Affairs (RA) teams to ensure audit readiness. - Review and approve analytical method transfer and validation protocols. - Lead internal quality audits and support external inspections. - Provide guidance and mentoring to junior analysts and Assistant Quality Assurance (AQA) staff. Perks and benefits As per company standard
Role & responsibilities Production 1. To monitor all production activities of production department. 2. To plan department production schedules according to marketing requirement. 3. To co-ordinate with Plant Head and Stores-In-Charge for procurement of raw and packing materials required for production. 4. To approve all raw/packing material indents for batch manufacturing of products. 5. To plan monthly production schedules and make necessary changes in day to day schedules whenever required 6. Ensure optimal usage of manpower for carrying out different activities in the department. 7. To co-ordinate with maintenance department regarding the utilities requirement and its performance. 8. To co-ordinate with Q.C. department for approval of Raw Materials/Semi Finished/Finished products. 9. To co-ordinate with Q.A. in preparation of MMR's, BMR's/ BPRs and SOP's. 10. To co-ordinate with concerned agencies for validation of critical areas and equipment. 11. To co-ordinate with Q.A. for validation of equipment and preparation of SOPs. 12. To follow cGMP in all areas of production. 13. To co-ordinate with product development during processing of new products. 14. To ensure that all BMR's and other production documents are maintained as per requirement. 15. To maintain discipline in the production areas. 16. To ensure safety of workers and other staff in departments. 17. To ensure that manufacturing and other operations are carried out as per the laid down procedures in MMR's and SOP's. 18. To co-ordinate with maintenance department for general preventive maintenance and breakdown maintenance. 19. To appraise Plant Head /Management regarding day-to-day production activities. 20. To train and arrange training for personnel. 21. To ensure hygiene in all areas of production and hygiene of personnel in the department. 22. To delegate responsibilities to subordinates whenever required. 23. To ensure that proper batch yields are obtained. 24. To indent for consumables and miscellaneous items required for production. 25. To carry out any other duties assigned by Plant Head. 26. Responsible for the day - today production planning. 27. Work assignment to production executives as per production planning. 28. Monitoring the GMP documents like equipment logbooks/sheet, records of daily activity, housekeeping etc. 29. Online filling of BMR, BPR of the batches and review of the same. 30. Preparation of Monthly report, production planning and Implementation, Yield improvement, Optimum Capacity Utilization, Productivity Improvement, Reduction of Wastage. 31. Periodic audit of all the activities / operation of the plant ensure statutory compliance / In-house standard compliance. 32. Submitting consolidated monthly report on all aspects of Plant operations to the Administrative Director. Preferred candidate profile only Candidates with Pharma experience are requested to apply. Perks and benefits Commensurate with experience and performance track record-will not be a constraint for the right candidates
1. : Identify, vet, and build strong relationships with reliable suppliers and vendors. 2. Work with departments to understand needs, source materials, goods, and services. Annual bonus Leave encashment Health insurance
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