Role & responsibilities Manage and monitor stock levels of raw materials, packaging, and finished goods to ensure sufficient supply and prevent overstocking. Maintain accurate records of all received, stored, and dispatched materials. Oversee the proper layout of materials, often using ABC analysis for efficient storage. Supervise all daily warehousing activities to ensure efficiency. Monitor material consumption and inventory variances. Ensure readiness for internal and external audits. Ensure the store complies with Good Manufacturing Practices (GMP), Good Hygiene Practices (GHP), and other regulatory requirements. Maintain the store's cleanliness, organization, and adherence to safety standards. Lead, supervise, and train store staff to promote safety, quality, and efficiency. Coordinate with other departments such as Production, Quality Assurance, and Purchase to ensure timely material availability. Implement and enforce security measures to prevent theft and ensure store safety. Maintain material handling equipment and ensure the store is well-maintained. Preferred candidate profile Strong understanding of GMP and quality control procedures. Proficiency in inventory management systems and data analysis. Excellent leadership and staff management skills. Strong communication and interpersonal skills for interdepartmental coordination. A proactive approach to identifying and resolving issues.
Role & responsibilities Responsible for all in process Quality Assurance Activities Document issuance and control Preparation and review of SOPs, Protocols, Reports, BMR, BPR and QC Specifications Issuance and review of BMR and BPR and other quality system documents Internal audit and its compliance related activity Ensuring compliance to cGMP Prepare Annual Training Plan in co-ordination with Head of QA Schedule and coordinate the cGMP training session Assist in the delivery of new employee orientation training Assure training records are maintained for regular, temporary and contractors/consultants Check monthly log book and calibration of IPQA instrument and balance Stability and control sample management Preferred candidate profile Should be worked in QA Department Well versed with computers, MS officer knowledge is must. documentation skills required
Role & responsibilities Opportunity to open the new countries with new buyers Maintain the current export sales and ensure the current product approvals / re-approvals Selections of products as per the requirement of overseas buyers and Minimum three meetings in a year with overseas buyers to enhance the business Ensure to coordinate with RA and submission of dossiers to overseas buyers and authorities in time Co-ordination with various Depts. for samples, regulatory requirements, DMFs and other documentation for new customer & regulatory approvals to meet statutory requirements of the country Assist the team in day to day activities to ensure smooth functioning of the businesses and in the monthly order forecasting for production planning. Manage business development activities to add new customers and increase market coverage of existing range of products in untapped regions and new countries Identification of markets and customers for new products and products in pipe-line. Assist the Executive Director for a successful launch and in ensuring sales of new products once commercialized. Interact with regular customers to ensure continuity of existing businesses - from the time that orders are received to the time shipments are dispatched as per customer requirement. Co-ordination with the planning / production and Export Logistics/Shipping team to ensure dispatch as per customer time-lines, export shipping documentations are provided to the customer and ensure payments are received by due-dates from the customer. Provide market research, market intelligence and key information on international market trends and competition to help the division with future export strategies. Preferred candidate profile Experience in Formulation based pharmaceuticals product marketing and sales in Domestic Market Minimum knowledge of 2 and more country's product, disease pattern, segment, trend, Documentation, Marketing and sales method experience in Pharma companies as managerial capacity, Handling Marketing team and trained them for progress in the targets given by the company
Role & responsibilities 1. Interact with regular customers to ensure continuity of existing businesses 2. Co-ordination with the planning / production and Export Logistics/Shipping team to ensure despatch as per customer time-lines 3. Creation of export shipping documentations 4. Ensure payments are received by due-dates from the customer. 5. Co-ordination with various Depts. for samples, regulatory requirements, DMFs and other documentation for new customer & regulatory approvals to meet statutory requirements of the country 6. Assist the HOD in day to day activities to ensure smooth functioning of the businesses and in the monthly order forecasting for production planning. 7. Assist the HOD for a successful launch and in ensuring sales of new products once commercialized. 8. Maintaining and housekeeping of sales database and generating sales reports Preferred candidate profile Should be able to work in the team. Quick Learner Passionate, self-driven, Self Motivated Result oriented, qualitative on time delivery Resilient, adapt to change, curious to seek and share knowledge, learning and best practices
To check and monitor the GMP and GLP compliances. Dispatch of goods from plant - completion of all documentation and give the batch release To be responsible for overall quality assurance functions in the factory. To approve and monitor all SOPs related to QA, QC, Production, stores, Admin and Engineering departments. To approve all specifications of Raw Materials, Packing Materials, Intermediates and Finished Goods. To review and approve Validation Master Plan, Master Formula Records, Master BMR, Master BPR, Site master files. To approve and monitor all process validations, Cleaning validations, Hold Time Studies, Validations of premises, equipment and procedures. To approve the stability programme and procedure. To carry out the internal and external audits and to monitor the compliances of regulatory audits. To release the finished product after verifying the Batch manufacturing and packing records, analytical records and other related documents thereof. To design and approve the training schedule & impart training to all personnel. To check and approve the preventive maintenance schedule. To check for the sanitation of premises and equipment, hygiene & housekeeping of factory. To check and approve deviations, change controls, OOS, Investigation reports, all IPQA records and annual product reviews. To handle market complaints, FDA related matters and FDA complaints, product recalls and quality management systems activities. To monitor compliances for systems and documents and ensure all legal standards are met. To monitor the effectiveness and efficiency of HVAC, water system, Compressed air and all utilities used in the manufacturing of products. To monitor the formulation development and technology transfer activities from R&D and ADL To Confirm Quality Assurance at every stage of Product Processing. Responsible for handling and monitoring of control samples and upkeep of control samples room.
Role & responsibilities Create and maintain production schedules to meet targets and ensure efficient resource utilization. Communicate with procurement for raw material availability, with the quality assurance (QA) and quality control (QC) departments for checks and validation, and with engineering for equipment maintenance. Monitor production processes to ensure efficiency, troubleshoot issues to minimize downtime, and implement continuous improvement initiatives. Ensure all production activities comply with pharmaceutical industry regulations, Good Manufacturing Practices (GMP), and internal quality standards. Supervise and train production staff, motivating them to achieve targets while adhering to quality and safety protocols. Generate production reports, analyze data, and review key performance indicators (KPIs) to identify areas for improvement. Manage inventory levels to prevent shortages and overstocking, ensuring a smooth flow of materials. Preferred candidate profile Prior experience in production operations within the pharmaceutical industry is essential. The ability to lead and motivate teams, along with excellent communication skills to interact with various departments, is crucial. Strong analytical and problem-solving abilities are needed to identify issues and implement solutions Deep understanding of pharmaceutical production processes, equipment, and regulatory requirements (e.g., GMP).
Role & responsibilities Creating new designs of Brochures, Visualaids, LBLS, Mailers and Pamphlets. Modifying and finalizing pharmaceutical packaging designs like boxes, foils, inserts and tubes Corel DrawX6, Adobe Photoshop CS4, Adobe Illustrator CS4, Adobe PageMaker (all latest version knowledge required) Get final Approval from the export department before printing Preferred candidate profile BA/Bcom with good hands on graphic designing Employee who has worked in pharma company for minimum 3yr will be essential
Role & responsibilities Responsible for all in process Quality Assurance Activities Document issuance and control Preparation and review of SOPs, Protocols, Reports, BMR, BPR and QC Specifications Issuance and review of BMR and BPR and other quality system documents Internal audit and its compliance related activity Ensuring compliance to cGMP Prepare Annual Training Plan in co-ordination with Head of QA Schedule and coordinate the cGMP training session Assist in the delivery of new employee orientation training Assure training records are maintained for regular, temporary and contractors/consultants Check monthly log book and calibration of IPQA instrument and balance Stability and control sample management Preferred candidate profile Should be worked in QA Department Well versed with computers, MS officer knowledge is must. documentation skills required
Role & responsibilities Create and maintain production schedules to meet targets and ensure efficient resource utilization. Communicate with procurement for raw material availability, with the quality assurance (QA) and quality control (QC) departments for checks and validation, and with engineering for equipment maintenance. Monitor production processes to ensure efficiency, troubleshoot issues to minimize downtime, and implement continuous improvement initiatives. Ensure all production activities comply with pharmaceutical industry regulations, Good Manufacturing Practices (GMP), and internal quality standards. Supervise and train production staff, motivating them to achieve targets while adhering to quality and safety protocols. Generate production reports, analyze data, and review key performance indicators (KPIs) to identify areas for improvement. Manage inventory levels to prevent shortages and overstocking, ensuring a smooth flow of materials. Preferred candidate profile Prior experience in production operations within the pharmaceutical industry is essential. The ability to lead and motivate teams, along with excellent communication skills to interact with various departments, is crucial. Strong analytical and problem-solving abilities are needed to identify issues and implement solutions Deep understanding of pharmaceutical production processes, equipment, and regulatory requirements (e.g., GMP).
1. Overall maintenance of Plant (Civil, Electrical and Mechanical) 2. Increase efficiency by planning, delegation and governance 3. Coordination with vendor, contractor or third party to deliver optimal output within budget and timeline 4. Coordination with various departments within company for smoothen the day to day operation 5. Reduce the incidence of costly breakdowns and develop strategies to improve overall reliability and safety of plant, personnel and production processes. 6. Ensure continuous running of equipment and machinery 7. Ensure that all machinery need to be well conditioned and well maintained at all the time 8. Participate in various audit (WHO, PICS etc.) 9. Supervision and maintenance of machinery used in the production of various pharmaceutical dosage forms (tablets, capsules, injectables, devices, and bio-pharmaceutical devices. 10. Proactive and Troubleshooting of issues faced by machinery. 11. Safety procedures and proper organization must be maintained in all areas always. 12. Installation and maintenance of machinery for example Boiler, AHU, chiller, air compressor, granulator, tablets, syrup making and packing machine etc. 13. Handled HVAC and water systems Preferred candidate profile 1. BE (Mech or Electrical) with pharmaceutical experience of 5 to 10 yrs 2. Have knowledge of utility equipment (Boiler, AHU, chiller, air compressor etc.) and face external Audit independently 3. have worked on maintenance & installation of machinery used in the production of various pharmaceutical dosage forms (tablets, capsules, injectables, devices, and bio-pharmaceutical devices)