583 Executive Jobs - Page 3

Job responsibilities ● Assisting the store manager in executing store operations during scheduled shifts. ● Acts with integrity, honesty, and knowledge that promote the culture, values, and mission of Bakingo. ● Maintains a calm demeanor during periods of high volume or unusual events to keep the store operating to standard and to set a positive example for the shift team. ● Anticipates customer and store needs by constantly evaluating the environment and customers for cues. ● Communicates information to the manager so that the team can respond as necessary to create a safe working environment during each shift for his/her staff and customers. ● Assists with new staff training by positively reinforcing successful performance and giving respectful and encouraging coaching as needed. ● Creates a positive learning environment by providing clear, specific, timely and respectful coaching and feedback to team/new hires on shift to ensure operational excellence and to improve overall team performance. ● Delivers legendary customer service to all customers by acting with a customer comes first attitude and connecting with the customer. ● Develops positive relationships with the shift team by understanding and addressing individual motivation, need and concerns. ● Executes store operations during scheduled shifts. ● Organizes opening and closing duties as assigned. ● Follows Bakingo operational policies and procedures, including those for cash handling and safety and security, to ensure the safety of all staff during each shift. ● Maintains regular and consistent attendance and punctuality. ● Provides quality beverages, whole bean, and food products consistently for all customers by adhering to all recipe and presentation standards. ● Follows health, safety and sanitation guidelines for all products. Skills and Qualifications: ● Attention to detail ● Coaching skills ● Works well under pressure ● 0-3 years experience(as per role requirement) ● Strong planning skills ● Good communication skills Motivational skills ● Punctual Job Type: Full-time Pay: ₹13,000.00 - ₹15,500.00 per month Benefits: Health insurance Paid sick time Provident Fund Work Location: In person

Company Description At Food Whisperer, we craft exceptional corporate dining experiences by blending sustainability, farm-to-table sourcing, and advanced food technology. Drawing from over two decades of expertise in premium corporate catering as part of The House of Khansamas, our mission is to deliver diverse, high-quality, and eco-conscious culinary experiences. With a focus on freshness and efficiency, we prepare over 500,000 meals daily and aim to expand to 10 mega kitchens across 9 cities by 2026. Our team of 375+ professionals uses AI-driven kitchen operations to ensure nutritious and tailored meals for modern workplaces. Role Description This is a full-time on-site role for an HSEQ Executive located in Noida. The HSEQ Executive will be responsible for overseeing and implementing health, safety, environmental, and quality standards across all operations. Day-to-day tasks include conducting risk assessments, ensuring compliance with regulations, developing and maintaining safety programs, and leading training sessions. The role also involves regular audits, incident investigations, and continuous improvement initiatives to elevate operational standards. Qualifications Knowledge of health, safety, environmental, and quality regulations Experience in conducting risk assessments and incident investigations Ability to develop and implement safety and quality programs Strong audit and compliance skills Excellent communication and training capabilities Attention to detail and analytical problem-solving skills Experience in the food industry is a plus Bachelor's degree in Environmental Science, Occupational Health and Safety, or related field

Date: 12 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Role-specific Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM. Attend the training session of EHS, cGMP and HRD. Ensure process equipment's/instruments are in Qualified in state. Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution. Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks. Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records. Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve. Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Technical /Functional Skill Expertise in Upstream unit operations (CHO based mammalian expression systems). Strong Hands on experience with SUB (Up to 2000 L scale) Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area. Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects Experience on risk assessment tools and change management. Experience on the Equipment Qualification and commission aspects

Date: 12 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Role-specific Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM. Attend the training session of EHS, cGMP and HRD. Ensure process equipment's/instruments are in Qualified in state. Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution. Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks. Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records. Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve. Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Technical /Functional Skill Expertise in Upstream unit operations (CHO based mammalian expression systems). Strong Hands on experience with SUB (Up to 2000 L scale) Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area. Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects Experience on risk assessment tools and change management. Experience on the Equipment Qualification and commission aspects

A GRN (Goods Received Note) Executive's primary responsibility is to accurately record and manage the receipt of goods into a warehouse or storage facility. This includes creating GRNs in the relevant system, matching delivery challans and invoices with physical receipts, and ensuring proper documentation and labeling of materials. They also play a crucial role in inventory management by reporting discrepancies and maintaining GRN logs for audit and reporting purposes. Key Responsibilities of a GRN Executive: https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=GRN+Creation&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIDBAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Generating accurate GRNs for all incoming goods, often within an ERP or inventory management system like Tally. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Matching+Documentation&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIExAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Verifying and matching supplier delivery challans and invoices with the actual received goods. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Inventory+Management&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIDRAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Ensuring the correct specifications, quantities, and documentation of received materials. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Quality+Control+Coordination&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIEBAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Working with the Quality Control (QC) team to inspect goods before GRN entry. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Material+Labeling&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIEhAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Properly tagging and labeling materials according to the warehouse system. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Discrepancy+Reporting&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIFBAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Identifying and reporting shortages, damages, or mismatches to the relevant teams (e.g., purchase, QC). https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=GRN+Log+Maintenance&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIDxAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Maintaining organized GRN logs for auditing and reporting purposes. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Price+Board+and+Barcode+Management&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIDhAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : In some cases, updating price boards and barcode information related to received goods. https://www.google.com/search?rlz=1C1RXQR_en&cs=0&sca_esv=16d5bc79565112ea&sxsrf=AE3TifP3vNPacAN5uWUJ3eDGov_fI0WcUA%3A1755159454437&q=Coordination+with+Other+Departments&sa=X&ved=2ahUKEwjg0YG-7omPAxVZUGwGHXHXLLEQxccNegQIERAB&mstk=AUtExfBQabTLcUeyvCxgvDQ8t3wH1zA1qLEwI73_GtLj2L9Noq8A_blG885uZKDXqWdcDW1-vv0erR2S45Pk2WxNYaa5prZNklF0WYnjGeN6N-D2ombSJpqypCHFVUqDCZ6hEXNutHpjiekByiK7rgqCCRL9hlreNvMu6CsEf-DC5k1sDQI&csui=3 : Communicating with other departments (e.g., purchase, accounting) regarding GRN-related issues or queries.

Sales Coordinator (Female Canddiate Only) Job Location - Mumbai (Nearest Stations - Church Gate and CSMT) Key Responsibilities Prepare and maintain sales reports, databases, and presentations. Order Booking Preparation of quotations Data mining for export market Manage data entry and ensure accuracy of sales records. Draft and respond to professional emails. Coordinate with internal teams, plant and clients for smooth operations. Requirements Key Requirements Graduate Female candidate Fluent in English communication (Both verbal and written) Ready to work occassionally beyond office hours to match international timings Proficiency in MS Excel, Word, PowerPoint, and email communication. Strong organizational skills and attention to detail. Prior experience in sales coordination or administrative support of 3-4 years Open for new learnings

i have work in full time job

Job Title: Material Expeditor Position Summary The Material Expeditor is responsible for ensuring the timely delivery of materials, components, and equipment from suppliers to support ongoing operations and projects. Based at the Head Office, this role involves close coordination with suppliers, internal teams, and logistics providers to track orders, resolve delays, and maintain accurate delivery schedules. Key Responsibilities Order Follow-up & Tracking Monitor purchase orders to ensure timely delivery of goods. Maintain updated records of order status, shipment schedules, and delivery dates. Follow up with suppliers regularly to confirm manufacturing and dispatch timelines. Supplier Coordination Act as the main contact point between the company and suppliers for expediting purposes. Resolve any issues or bottlenecks that may cause delays. Request and review shipping documents, packing lists, and compliance certificates. Logistics & Delivery Management Coordinate with freight forwarders, customs agents, and warehouse teams for timely receipt of goods. Ensure proper documentation is available for customs clearance and internal processing. Track in-transit shipments and address delays proactively. Internal Liaison Communicate delivery schedules and any changes to project, operations, and warehouse teams. Support procurement and planning teams with lead-time forecasts and delivery performance data. Reporting & Documentation Maintain expediting logs and dashboards for management review. Prepare weekly/monthly reports on supplier delivery performance and order status. Assist in updating ERP/MRP systems with accurate delivery data. Qualifications & Skills Education: Bachelor's degree in Supply Chain, Logistics, Business Administration, or related field. Experience: 2–5 years in expediting, procurement follow-up, or supply chain coordination (preferably in manufacturing, construction, or engineering industries). Skills Strong communication and negotiation skills. Proficiency in MS Office and ERP systems (SAP, Oracle, etc.). Attention to detail and ability to work under tight deadlines. Knowledge of international shipping terms (Incoterms) and documentation. Key Competencies Proactive problem-solving Strong organizational skills Ability to manage multiple priorities Collaborative team player with a customer service mindset

Company Description Paramount Health Services & Insurance TPA Pvt. Ltd. (PHS) is a leading Third Party Administrator (TPA) in the Health Insurance sector, servicing all insurance companies. PHS enhances health insurance policies for individuals by adding value through a network of healthcare service providers, medical care standardization, claims management, client servicing, and expert opinion. PHS customizes healthcare delivery to administer comprehensive healthcare packages for its clients. Role Description This is a full-time on-site role for an Executive, located in Mumbai. The Executive will be responsible for day-to-day operations including client servicing, claims management, coordination with healthcare service providers, and ensuring compliance with medical care standards. The role involves liaising with various stakeholders, managing healthcare delivery packages, and providing expert opinions to ensure smooth operation of health insurance policies. Qualifications Strong skills in client servicing and relationship management Experience in claims management and coordination with healthcare providers Knowledge of medical care standards and healthcare delivery Excellent communication and interpersonal skills Ability to work independently and in team settings Problem-solving and analytical abilities Experience in the health insurance sector is a plus Bachelor's degree in Healthcare Management, Business Administration, or a related field

Executive with good communication, smart looking and willing to work in target based team

The Executive position at Buffcon, located in Bihar, is a full-time on-site role where you will be responsible for overseeing daily operations, managing staff, and ensuring adherence to company policies and procedures. Your role will involve developing and implementing strategies for business growth, managing budgets, and engaging with stakeholders. Furthermore, you will analyze performance metrics to identify areas for improvement and uphold customer satisfaction. To excel in this role, you should possess leadership, management, and supervisory skills. Your strategic planning and business development capabilities will be crucial, along with financial management and budgeting proficiency. Effective communication, negotiation, and interpersonal skills are essential for successful performance. Additionally, your problem-solving and decision-making abilities will be valuable assets in this position. Previous experience in team management and collaboration with cross-functional teams will be advantageous. A Bachelor's degree in Business Administration, Management, or a related field is required to qualify for this role.,

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of finished goods to distributors, C&F agents, or export destinations. Liaise with transporters, courier agencies, and freight forwarders. Prepare and verify shipment documents including invoices, packing lists, COAs, MSDS, etc. Vendor & Supplier Management Maintain relationships with existing suppliers and evaluate new suppliers based on quality, cost, delivery, and service. Support vendor qualification audits in collaboration with QA/QC. Compliance & Documentation Ensure SCM activities adhere to cGMP, GDP, and other regulatory requirements. Maintain records as per SOPs and support internal/external audits. Coordination & Reporting Work closely with production, QA/QC, and finance teams for smooth SCM operations. Prepare and present periodic reports on procurement, inventory status, and supply chain performance.

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of finished goods to distributors, C&F agents, or export destinations. Liaise with transporters, courier agencies, and freight forwarders. Prepare and verify shipment documents including invoices, packing lists, COAs, MSDS, etc. Vendor & Supplier Management Maintain relationships with existing suppliers and evaluate new suppliers based on quality, cost, delivery, and service. Support vendor qualification audits in collaboration with QA/QC. Compliance & Documentation Ensure SCM activities adhere to cGMP, GDP, and other regulatory requirements. Maintain records as per SOPs and support internal/external audits. Coordination & Reporting Work closely with production, QA/QC, and finance teams for smooth SCM operations. Prepare and present periodic reports on procurement, inventory status, and supply chain performance.

" Responsible For rDNA manufacturing and Parenteral mfg activities at Dholka premises To ensure personal hygiene of the workmen before entering to aseptic area and maintain record. To check and ensure that aseptic area workmen are following entry exist procedure properly. To check and ensure that differential pressure, RH and temperature of the aseptic area and mfg area are within limit and record it properly. To check and ensure that differential pressure of all Laminar Air Flow are within limit and record it properly. To check on line in process parameters like temperature, RH, fill volume, quality of sealing at specific interval as mentioned in respective MMDI and SOPs and record the same in BMR To do compounding activities and dispensing activities. To check the vial washing machine, vial dehydrogenation tunnel, vial filling machine, vial sealing machine operation. To check the autoclave and automatic vial Inspection machine operation. To maintain equipment logs as per SOP To ensure proper inter personal relationships (IPR) in the section. To review daily production and to discuss other issues. To ensure proper cleaning of the mfg areas. To ensure proper status labeling as per Sop. To ensure the all required documents to comply cGMP. To ensure calibration certificates of all measuring instruments comply with norms. To ensure concurrent documentation of all production processes undertaken. To ensure plant wide cGMP compliance."

" Responsible for compression activity in Penicillin department. To enforce CGMP compliances in the department. To maintain higher standard of quality during compression. To coordinate interdepartmental and resolve the issues pertaining to product. To improve the productivity. Production planning so as to meet the effective implementation of Plan To discuss and give feedback on day to day production planning for any shortage to department. To review daily production and to discuss other issues. To complete BMR of daily production & transfer finished goods on daily basis. To coordinate with Eng. Department for preventive maintenance of various machine also Report and follow up on breakdown maintenance. Ensure proper cleaning in Penicillin area. To ensure the all required documents to comply CGMP. To ensure concurrent documentation of all production processes undertaken. To raise Change Control, CAPA & Deviation in LIMS as per requirement. To ensure proper documents & status labeling as per the requirements of audit. To done SAP entry on daily basis. Prepare departmental SOP as per requirement. To give training to subordinate & worker as per training colander & enter data in TIMS as Per requirement."

Execution of plans for cell culture group Preparation of media for cell culture purpose Preparation of buffers Cell Line maintenance Calibration of pH meter Handling and knowledge of Bioreactor (STR and Wave) Cell propagation for different projects Performing Cell Count and metabolite analysis. Compiling of data, forms and report preparation Aseptic handling and sterile Area Maintenance Maintaining inventory of cell culture related products SOP preparation and periodic revision

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of finished goods to distributors, C&F agents, or export destinations. Liaise with transporters, courier agencies, and freight forwarders. Prepare and verify shipment documents including invoices, packing lists, COAs, MSDS, etc. Vendor & Supplier Management Maintain relationships with existing suppliers and evaluate new suppliers based on quality, cost, delivery, and service. Support vendor qualification audits in collaboration with QA/QC. Compliance & Documentation Ensure SCM activities adhere to cGMP, GDP, and other regulatory requirements. Maintain records as per SOPs and support internal/external audits. Coordination & Reporting Work closely with production, QA/QC, and finance teams for smooth SCM operations. Prepare and present periodic reports on procurement, inventory status, and supply chain performance.

Major Purpose of the Job: Development of purification process for recombinant proteins. Principal Tasks and Responsibilities: Stock buffers and working buffer preparation pH and conductivity meter operation Column packing for purification Column cleaning (Pre and post run CIP), maintenance and storage Independently handle protein purification system example AKTA purification system Protein concentration using TFF, and different concentration system Documentation and preparing presentations of data generated. Ensuring good laboratory practices in DSP In the absence of the job holder the designee assigned by the reporting manager would be responsible for carrying out the above responsibilities.

" Compliance to cGMP and other regulatory requirement. To monitor the daily packing activates in primary packing in with compliance of cGMP norms. To execute packing inputs as per shift plan in Advanced & achieve it. Ensure compliance of the online Documents during packaging process. To ensure the packing activity as per Respective SOP. To Monitor & Minimize the process loss during packing operation. Perform the In process checks for the Correctness of the packed Product. Stage wise Reconciliation of the Product/Packing material. Coordination with the Different Supportive department for the fulfilment of the Department requirement."

To perform the technology receiving activities and QMS related activities at the manufacturing plant. To perform technology-receiving activities by receiving processes from upstream process development to manufacturing and/or between multiple manufacturing sites. This includes developing and maintaining key SOPs, manufacturing records to support compliance with quality management and regulatory submissions. To perform alternate vendor batch execution, process improvement, change in batch size, trouble shooting at shop floor, equipment change activities of product after technology transfer completion along with production team. To coordinate the development of the manufacturing process with the R&D by keeping in mind scale-up issues, process specifications, and operating procedures for new products, new equipment, and technologies for successful product receiving. Work out on finalizing batch sizes of scale up, exhibit and commercial batches to meet the equipment capacities and regulatory requirements with consent of R&D and production. To prepare/review relevant documents like SOP, Batch Manufacturing Record, Sampling Protocol, hold time study protocol/ report, stability study protocol/report, Process validation protocol and Report for the scale up, exhibit and validation batches. To provide technical support for change management, investigations of deviations or OOS, CAPA identification and QMS related activities at plant. To provide technical support for CMC section of ANDA submissions or other regulatory agency documents prior to forwarding to the Regulatory Affairs for inclusion in the supplement submission. Principal task and responsibilities: Ensure cGMP and Regulatory compliance. To cross check the online documents periodically to ensure the good document practice. To rectify any activity which is making adverse effect on productivity or quality, in consultation with QA Department. To ensure discipline from co-workers and get systematic work to improve quality. Arrange CFT meeting to resolve day to day issues. Involve in closure of change control note, deviation and give guidance to ensure that it is complete in time.

" Responsible for small volume parenteral manufacturing activities at Dholka premises. To check hygienic condition of the workmen before entering to aseptic area, processing area and compounding area and maintain record. To check and ensure entry exist procedure of workmen with proper gowning and sanitization. To check and ensure that Temperature and differential pressure of the all area is within limit and record it properly. To check on line in process parameters like temperature, RH, fill volume, quality of sealing at specific interval as mentioned in respective MMD-I and SOPs and record the same in BMR To check and ensure that sterilization of the containers, equipment's, utensils etc. are as per respective SOPs. To maintain equipment logs as per SOP To ensure proper cleaning of the working areas. To ensure proper status labeling as per Sop. To ensure calibration certificates of all measuring instruments comply with norms. To ensure plant wise cGMP compliance."

Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. Logistics & Distribution Ensure timely dispatch of finished goods to distributors, C&F agents, or export destinations. Liaise with transporters, courier agencies, and freight forwarders. Prepare and verify shipment documents including invoices, packing lists, COAs, MSDS, etc. Vendor & Supplier Management Maintain relationships with existing suppliers and evaluate new suppliers based on quality, cost, delivery, and service. Support vendor qualification audits in collaboration with QA/QC. Compliance & Documentation Ensure SCM activities adhere to cGMP, GDP, and other regulatory requirements. Maintain records as per SOPs and support internal/external audits. Coordination & Reporting Work closely with production, QA/QC, and finance teams for smooth SCM operations. Prepare and present periodic reports on procurement, inventory status, and supply chain performance.

Follow cGMP and GLP PRACTICES. To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly. To follow safety Procedure in QC department. To manage an accurate, reliable, efficient and timely review of finished products, in process/ validation, raw material, stability, GLP, Non-routine samples. To ensure timely review of batch audit trail, system audit trail, message center. To ensure review of Logbooks of instrument, equipment’s, columns, standards, impurities etc. To review the COA of finished product in LIMS after the completion of analysis. To ensure the status label updated for the instruments, equipment, glassware and workplace. To conduct the training program to analyst as per the training calendar. To ensure the training about the changes in standard operating procedures (SOP), if required. To ensure the Sequence of HPLC/GC/IC are reviewed prior to start of the sample set. To ensure methods are prepared accordingly STP/SOP. To ensure proper integration and reviewed prior to E- signature of data by reviewer To do any other Work assign by HOD.

1 Ensure Freedom to operate of CPL's product (Formulation) 2 Design a strategy to secure CPL's invention effectively 3 Handling of Patent Prosecution 4 Effective Management of CPL Patent Portfolio 5 Support to New Product Selection Activity

Ensure Freedom to operate of CPL's product (Formulation) Design a strategy to secure CPL's invention effectively Handling of Patent Prosecution Effective Management of CPL Patent Portfolio Support to New Product Selection Activity