Position: Senior Manager 2 Job Title: Plant Project Management (Technology Transfer) Function: Manufacturing (FN0066) Sub-function: Formulation Production Location: Sikkim II -Operation Job Summary Accountable for timely execution of New Product Launch and Site transfer product. Co-ordinate with corporate project management team / MSTG / RnD / Quality /IRA for seamless execution of transfer and product manufacturing Areas of Responsibility Planning and execution of new lunch product/exhibit batches on time at site. Accountable for timely execution of site transfer product. Co-ordinate with corporate project management team & MSTG team and relevant stakeholders for smooth functioning of new product lunching activities. Support Manufacturing team for Process improvement by innovation and validation during course of manufacturing in new products as well as legacy products. Work closely with CFT for Product robustness. To participate and review the quality system documents like change control, deviation, investigation, CAPA and market complaint etc. Participate in Internal / CQA audit or any other regulatory body audit to ascertain compliance. Job Requirements Educational Qualification : BPharm / MPharm Skills : New Product Project Management, Technology Transfer ,Product Robustness Experience : 12- 14 Yrs

Job Description: Technical Trainer specializing in Packaging Operations Course Development : Designing training material and presentations related to packaging operations. This includes creating content on topics like blister packing, Strip Packing, Pouch Packing, Bottle Packing, Cartonating, etc and labeling. Training Delivery : Conducting training sessions, workshops, and webinars for employees involved in packaging. The trainer ensures effective knowledge transfer and skill development. Unit Operations Expertise : In-depth knowledge of various packaging unit operations: Blister Strip Pouch Sachet Bottle Cartonator Equipment Handling : Demonstrating the use of packaging machinery (e. g. , fillers, welders, labellers) and ensuring proper equipment maintenance. Process Troubleshooting : Addressing common issues encountered during packaging operations and providing solutions. Requirements and Skills : Proven experience as a technical trainer or subject matter expert in packaging. Excellent communication skills for effective training delivery. Familiarity with GMP (Good Manufacturing Practices) and quality control. Relevant technical degree or certification (e. g. , Certified Technical Trainer). Feel free to adapt this description to your specific needs!

Position: Manager - PMO Job Title: PMO Job Grade: G10 (Manager-1) Function: Sun Global Operations Sub-function: Manager s Job Title: Plant Head Skip Level Manager s Title: Function Head Title: Location: Guwahati No. of Direct Reports (if any) Job Summary PMO role is managing Projects at Site. Co-ordination with Other Departments, Product Launching, Site Project initiatives, Compliance etc. Areas of Responsibility 1. Product Transfer - Managing projects at site, Co-ordination with R&D / MSTG / PMO / Quality / ADD departments etc. 2. Site Project Initiatives - Managing Demand V/s supply Gap and initiatives to overcome these Gaps 3. Compliance - Cordination for improvement required. 4. Investigation of Products and Lead the same. 5. Establishing new procedures, maintaining and updating existing procedures in the Production department. 6. To assist establishing a system in accordance with Good Manufacturing practice guidelines and responsible for follow established /new procedures/ new procedures, maintaining and updating existing procedures in the department. 7. Preparation of Risk assessment for New/Existing product, Evaluation and Approval of Risk assessment. 8. Make daily reports to production manager /superiors on day to day activities concerning the department. 9. Coordination with other departments like Administration, Warehouse, Quality Control , Quality Assurance, Quality Engineering, MIS and Engineering for related activities 10. Responsible to co-maintain, co-ordinate for validation and GMP in all departments along with the Quality Assurance officer and to co-ordinate with Quality Control department in matters relating to product quality. 11. Training the subordinates and manpower to meet the organizational goals and achieve GMP compliance. 12. To co-ordinate with the R & D / MSTG department for planning and execution to trail and exhibit batches along with New launches products Travel Estimate Job Scope Internal Interactions (within the organization) External Interactions (outside the organization) Geographical Scope Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification B. Pharm Specific Certification Skills Experience 14 to 15 Yrs

Role & responsibilities :- Candidate is primarily responsible for but not limited to: 1) ADR case triage and validity assessment: Perform triage of ADR cases for seriousness/follow up significance and identification of suspect products and events. Perform ADR case validity assessment. 2) Adverse Drug Reaction (ADR) processing Perform medical review of ICSRs Review of Literature Alerts and Medical Information Perform event listedness assessment to enable expedited reporting of ICSRs as per applicable regulatory requirements 3) Periodic Safety Report generation Medical Review of Periodic safety reports Medical review of line listings, query response, case correction. 4) Risk management Plan Preparation of Risk Management Plan 5) Other Pharmacovigilance projects Work in any other assigned Pharmacovigilance project Ensure compliance to applicable SOPs Maintenance of personal Pharmacovigilance record as per the applicable SOP Skills : Good Communication Skills, Awareness of global drug safety guidelines, sound medical knowledge, workflow management

Job Summary : We are looking for an experienced Sr. Manager to lead our API Utility Maintenance Management team. The successful candidate will be responsible for developing and implementing Utility maintenance strategies to ensure optimal performance, reliability, and compliance of API manufacturing Utility equipment and facilities Key Responsibilities: Develop and implement comprehensive utility maintenance management plans for API manufacturing utilities and facilities. Lead and manage a team of utility maintenance personnel, providing guidance and training on API-specific maintenance practices. Collaborate with cross-functional teams (Production, Quality, and Engineering) to identify and prioritize maintenance activities. Develop and manage maintenance budgets, ensuring cost-effective maintenance practices for API manufacturing utilities. Ensure compliance with regulatory requirements (cGMP, FDA, etc.) and internal quality standards for utility maintenance. Implement and manage preventive maintenance programs for API utilities, including scheduling, execution, and documentation. Conduct regular maintenance audits and risk assessments to identify areas for improvement. Develop and implement corrective actions to address utility maintenance-related issues. Collaborate with external vendors and contractors to ensure effective utility maintenance support. Develop and maintain maintenance-related documentation, including SOPs, procedures, and records. Utility-Specific Responsibilities : 1. Develop and implement maintenance strategies for API manufacturing utilities, including: Boiler management, Steam generation and distribution systems Chilling plants Compressed air systems Nitrogen plants and its distribution Cooling water systems HVAC systems Water systems including WFI generation and distribution 2. Ensure maintenance activities are performed in accordance with API-specific regulations and guidelines (e.g., ICH Q7). 3. Collaborate with API production teams to identify and support in Utilitys maintenance-related issues impacting API quality and yield. Requirements: Bachelor's degree in Mechanical, Chemical Engineering. Minimum 8-15 years of experience in Utility maintenance management, in a API manufacturing environment. Proven experience in leading and managing maintenance teams, with a focus on Utilities maintenance. Strong knowledge of cGMP, FDA regulations, and industry best practices for API manufacturing. Excellent communication, leadership, and Utility Maintenance & project management skills. Ability to work in a fast-paced environment and prioritize multiple tasks. Desirable: Master's degree in Mechanical Engineering, Certification in maintenance management or a related field. Experience with computerized maintenance management systems (CMMS). Familiarity with lean manufacturing principles and Six Sigma methodologies.

Project Manager - Utility Projects Location: Baska Managers Job Title: Head Utility No. of Direct Reports (if any) 4 Areas of Responsibility: We are seeking an experience Project Manager Mechanical Engineering with expertise in utilities management and ISP 50001 standard s. The idea candidate will be responsible for engineering designs, project execution , and energy efficiency initiatives within manufacturing facility. Will look after small projects within the plant, should have worked for ISO 50001, Should have knowledge of engineering drawings. Project Management & Engineering Designs: Lead and manage engineering projects related to utilities, energy efficiency, and mechanical systems. Oversee the design, installation, and commissioning of mechanical and utility systems. Ensure compliance with GMP, ISO 50001, and regulatory specifications for utility systems. Collaborate with cross-functional teams, vendors, and contractors for successful project execution. Manage project budgets, cost control, and resource allocation for efficient execution. Proficiency in engineering designs (AutoCAD, SolidWorks, or similar software) Utility & Energy Management: Manage and optimize utility systems (HVAC, boilers, compressed air, water and steam systems) to enhace efficiency and sustainability. Identify and implement energy saving initiatives to reduce operational costs and improve sustainability. Conduct energy audits and assessments to track performance and suggest improvements Job Requirements Educational Qualification BE Mechanical Experience 12 TO 15 YEARS experience in formulations Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Effectively manage the Site QC activities and resources necessary to smoothly run the QC operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Control accountabilities at site. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. To approve and monitoring of the Capex/Opex and outside lab analysis. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams.To ensure that the response for Internal External audit observations is provided within stipulated time frame. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QC systems at the site. Handling of QMS documents as per respective SOPs in a timely manner.To establish, validate, upgrade and implement the quality management system. Act as System Owner and ensure laboratory computerized systems are validated for its intended use through its lifecycle and to ensure scheduled qualification/validation and calibration of equipment/laboratory instruments. To assign the roles, responsibilities and authorities for persons in Quality Control. To monitor and ensure that RM/PM/IP/FP/Micro are released in time to meet market/customers requirements and Lab is being operated as per approved procedure. Responsible for handling, approval and monitoring of application like SAP, EWS, Track wise, LIMS (4.1.3), Partners, Medhas and EDMS. Act as system owner for Laboratory computerized systems including LIMS 4.1.3 and ensure laboratory computerized systems are validated for its intended use throughout its lifecycle. To perform and complete the approval activity in Medhas by approving UAM for periodic access review in LIMS 5.0.1. Implementation of new ideas to help in improving the competitiveness between all QC personnel. To coordinate with CQ / ADD / PDD / CC / HR/ Production / RMS / PMS / BSR.

YOUR TASKS AND RESPONSIBILITIES Development of marketing and promotional plans for products to support the end consumer s need Monitor business performance and support the portfolio with the help of regular tracking Market intelligence through primary research and customer connect Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs; initiating and coordinating marketing activities and projects Presentation to staff and training field staff for the same Visiting national and international congresses, hospitals, and key opinion leaders (KOLs); Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy; Discussion partner for first, second, and third-line professionals such as general practitioners, medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies; Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations. Collaboration with internal & external media to ensure the proper execution of strategies WHO YOU ARE: Experience: 3 to 4 years of experience in Pharma Marketing Qualification: B. Pharma + MBA - Marketing OR Pharma. Management Therapy Exposure: Cardio-Diabetes Skills: Able to foster collaborative relationships Proven track record of launching and managing successful products Strong analytical and problem solving skills Proficiency in product management tools Good in communication and presentation Science driven marketing strategies Job Location: Sun House, Mumbai

YOUR TASKS AND RESPONSIBILITIES Development of marketing and promotional plans for products to support the end consumer s need Monitor business performance and support the portfolio with the help of regular tracking Market intelligence through primary research and customer connect Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs; initiating and coordinating marketing activities and projects Presentation to staff and training field staff for the same Visiting national and international congresses, hospitals, and key opinion leaders (KOLs); Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy; Discussion partner for first, second, and third-line professionals such as general practitioners, medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies; Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations. Collaboration with internal & external media to ensure the proper execution of strategies WHO YOU ARE: Experience: 1 to 4 years of experience in Pharma Marketing Qualification: B. Pharma + MBA - Marketing OR Pharma. Management Therapy Exposure: Cardio-Diabetes Skills: Able to foster collaborative relationships Proven track record of launching and managing successful products Strong analytical and problem solving skills Proficiency in product management tools Good in communication and presentation Science driven marketing strategies Job Location: Sun House, Mumbai

Ensure the Preventive maintenance, Shutdown maintenance of HVAC and EHS equipment. Monitoring the budgets to have control on allotted budget. Maintain the proper discipline within the department. Coordinating with vendor and contractors. Coordinating bills verification and processing. Ensure the PM SDM to be carried out as per schedule. Supervision of-in house projects. Follow all safety rules and -house projects. Follow all safety rules and cGMP GEP Working as a document coordinator for engineering to issue, archive maintain the document. To ensure that upkeep of all time readiness.

Position: Manager - Engineering & Projects Job Grade: G10/ G11A Location: Ahmednagar No. of Direct Reports (if any) 15 Nos Areas of Responsibility Job Responsibilities: Monitor, Track and perform scheduled maintenance activities such as preventive maintenance through SAP, earthing maintenance, alarm verification as per format and schedule. Attending all type of breakdowns related to process and utility equipment. Internal customer satisfaction by timely problem solving and maintenance. OPEX control and inventory management , up keeping the diesel records, electrical spare record, etc. Handle and monitor maintenance activities of process equipment and utility equipment such as DG sets, Transformers, UPS, PCC and MCC panels, etc. Handle QMS activities in Trackwise such as Change control, Deviations etc. Certified investigator in engineering department, to perform and support engineering related investigations. Co-ordinate and face the audits from electrical department such as regulatory audit, statutory audits, safety audits etc. Prepare BOQ for the projects, monitor and support the execution according to the planning. Checking of contractor bills as per measurements and raising the indents. Handle eCSP related activities in SAP and get the approval for the vendor service at site. Proposal of CAPEX ideas to be implemented at site and support for the execution. SOP revision and new SOP preparation in EDMS. Analysis of monthly parameters such as power consumption, utility reports etc. Exploring possibilities of energy conservation and implementation and contribution towards Improvements in energy management and execute ASPIRE projects 15. Certified coach for electrical department. To impart the scheduled and regular trainings to electrical and cross functional team members. 16. To attend the duties as per schedule. 17. To take assigned trainings in LMS. 18. Section In-charge for Electrical section. 19. To prepare returnable & nonreturnable gat pass in GPS system. 20. Planning, procurement and executing of the plant modification as per the site requirement. Co-ordination with Purchase team for procurement completion giving required input details Co-ordination with vendors for technical discussion- quote - drawing receipt and approval Educational Qualification : BE Electrical / DEE Specific Certification: MS-Office Excel- Presentation SAP Experience 12 + Years in API Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Head- Flow Chemistry Job Role : Head Flow Chemistry Job Grade : GM (General Manager) Job Location : Gurugram (Delhi) The incumbent will be leading a team of Organic chemists & Chemical Engineers with following job responsibilities Drive continuous improvement by leveraging Process Intensification technologies including flow chemistry to reduce cost, reduce waste, improve yield. Development & Scale up of new continuous flow chemistry based technologies with internal & external partners. Trouble-shooting of running technologies in plant. Prepare and submit all the technical documents to CMC-QA. Address regulatory queries of customers and provide data for DMF filing. To discuss IP related queries of customers with cross functional teams. To ensure the compliance by following GLP in lab. Contributing to and maintaining a comprehensive knowledge of organic chemistry and synthesis technology literature Working with CFT to deliver on project goals via collaboration and clear communication Qualifications & Experience : Organic Chemist /Chemical Engineer with minimum 5 years experience in a continuous flow chemistry related projects with over 18+ years of industrial experience is required Expert understanding of and significant experience in conducting continuous flow chemistry is required Expertise in usage of Corning, Chemtrix ,Coflore, Amar, Vapor Tec, PFR, CSTR etc Expertise in designing and scaling up multi step continuous process Strong analytical and chemical problem solving skills are required

Hi, We are having an opening for Senior Manager - SAP QM (Primary), and SAP PM (secondary), IT at our Mumbai location Job Summary : Desired Skills & Experience Candidate should have worked on SAP QM (Quality Management) module which includes experience in development/ support of QM peripheral systems like LIMS/ Trackwise/ Track and Trace etc. Minimum of 8-10 years of relevant experience in full cycle SAP implementation as well as in support projects. Preferably should have experience in implementation/ support of SAP QM at a Pharma company or GxP controlled Process industry environment, that includes exposure to computer system validation activity. Candidate should have secondary experience in SAP PM (Plant Maintenance) module which includes experience in development/ support. Minimum of 5 years designing and configuring QM module, and knowledge of the key integration points between the other SAP modules (MM and PP). Candidate should have experience in use of standard SAP Fiori apps, and development of custom apps and its necessary setups. Candidate should be proficient in planning and execution of data conversion activities, and build/ execution of the necessary data migration tools like LSMW, LTMC etc. The candidate should be well conversant with SAP tables, SAP query, writing Functional Specifications for custom developments to deliver innovative solutions Ability to multitask and manage multiple deliverables and projects at the same time. Ability to understand business processes from a customer perspective Ability to work in a team environment, effectively interacting with others Must be results oriented, and demonstrate adaptability, flexibility and resourcefulness. Areas Of Responsibility: Roles & Responsibilities * Facilitate the implementation and support of SAP Quality Management for SUN Pharma entities operated in SAP - ECC and S4 HANA including 3rd Party System Integrations. * Perform detailed analysis of complex business process requirements and provide appropriate system solutions; identify, interpret, validate and document customer requirements. * Facilitate workshops to collect business requirements. * Map client business requirements, processes and objectives; develops necessary product modifications to satisfy customers needs. * Design, customize, configure and testing of the module. * Identify gaps, issues and work around solutions. * Act as liaison with internal customer for troubleshooting: investigate, analyse, and solve software problems. * Handle changes or emergency transports as needed for high priority issues; Document functional designs, test cases and results. * Proactively identify and propose business process and/or system enhancements. * Provide consulting services on both new implementations and existing support projects. * Act as a liaison between the business functions and the technical team. * Provide ad-hoc training and user support as required. * Work self-directed and independently; may act as subject matter mentor to more junior members. Educational Qualification : BE/ BTECH/MBA Specific Certification : SAP Certification in SAP QM will be an added advantage Skills : SAP QM (primary skill), SAP PM (secondary skill) Experience : Min. 8 to 10 Years in SAP QM

Position: Executive R&D Quality, CMC QA _ Commercial QA Support Grade: G12A Job Location: Vadodara Job Responsibilities: (PE Center) 1. Review of protocol/reports (Pharmaceutical Equivalence Report and Comparative Dissolution Profile Report) and other analytical documents related to Pharmaceutical Equivalence (PE) Center. 2. Review of QMS documents (Out of Specification/ Lab event/Planned deviation /Un planned deviation/Investigations/ CAPA/Change control). 3. To assist in developing procedures / quality system and assure compliance of the same by identifying gap through document review and Audits. 4. Review of SOPs for the compliance of the cGxP requirements and monitoring its implementation. 5. To provide support for computerised systems implementation into PE center and act as Process Quality Lead (PQL) for Validation of computerized system. 6. Review of documents, approve discrepancy note and handle quality activities of Medicinal Product Store. 7. To assess the compliance level of PE center through Self Inspection / Internal Audit program. To support all time readiness for successful regulatory inspection at PE center. Desired Candidate Profile: M. Pharm / M. Sc. with 5-7years of experience in manufacturing QC / R&D Quality involved in GMP operation. Worked in GMP area and well aware about GMP requirements for as per FDA, ANVISA, HC. Good oral and written communication skill Shall be well versed and have experience on quality management system, review of AMV, AMT, PE Certificate, CDP Report, qualification, and analytical raw data review. Shall be well versed with OOS, OOT, Investigation, Deviation, CAPA management & ANVISA PE center requirement

To prepare and implement of SOP's, revison of SOP and their compliance. To face various audits like compliance , internal and external audits related to facility management. Manage Housekeeping services as per the GMP Requirement To ensure availability of various materials in stock like Uniform, housekeeping, santitizing and disinfectant agents. To arrange Pest control services in plant. Manage Housekeeping services as per GMP requirement To take various initiatives for beautification of plant. To impart and ensure trainings to be provided as per training calendar and records to be updated accordingly. Preparation o SOP's and change control and providing trainings, using available software's like EDMS, EDAMS, Track Wise and LMS. Data to provide accounts related to department for budget preparation. To ensure good quality canteen services to all employees as per company poilicy and guidelines. Prepare and execute all contracts of admin department that is Housekeeping, Pest Control, Laundry Services, Gardening etc. Verify Bills of vendors and ensure timely release of payment to prepare.

Responsibility for Chemical/ Instrumental testing of Raw materials sample. Responsible for assure the quality of Sun s products manufactured at Sun Pharmaceutical Industries Ltd for the domestic market as well as export to emerging markets. Responsible for system up-gradation as per CQ and regulatory guidelines To analyze and report the stability sample FG sample if needed. Monitoring of gowning and sanitation practices in area of operation. Monitoring of compliance of standard operation procedure for operation of analytical instrument. To operate the analytical equipment in quality control as per the allotment works in shift. To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices. To support the internal audit/Regulatory/FDA audit with best of practices Following all regulations of cGMPs as per schedule M. To maintain the safety procedure in handling analytical equipment and hazards. Completing the training assigned as per the training need identified by participating in trainings organized or self-reading. To calibrate the analytical equipment s as per the calibration procedure for assigned responsibility of calibration. To maintain the analytical equipment s and laboratories in good state of operation .To maintain the stock of working standard, column, reagent, chemicals, glass ware etc. To follow procedure for non-conforming result as it is applicable in SOP of OOT, Lab Incident OOS. To follow the administrative procedure of compliance with respect to term and condition for attendance, leave and other benefits .

Analysis of samples allotted for testing of raw materials by using analytical instruments like IR, HPLC, GC, AAS, Particle size, KF Coulometer and other instruments as per STP and approved protocols. Documentation of analytical data and calculation of results. Enter analytical results in SAP and generate the COA in SAP. Ensure compliance to cGMP requirements and laboratory procedures. Preparation and standardization of volumetric solutions and reagents.

Position: Officer / Sr. Officer - Peptide Plant Grade: G12C / G12B No. of Position: 4 No. Job Location: Ahmednagar Qualification: M. Sc. (Organic Chemistry) Experience: 5 to 7 yrs experience in Peptide manufacturing plant Job Profile To issue and receipt of raw materials for manufacturing of Peptide Products as per requirement. Charging of batches and carry out all operations related to process as per BMR and written procedures. To manufacture peptide products as per BMR and written procedures in Peptide plant Operations, Calibration, Cleaning and Maintenance of process equipment and recording their usage logs. Monitor Process and cleaning turn around time (TR) during synthesis and purification of Peptide products. Monitor process parameter and yield. Reduction in Solvent usage and reduction in down time of the instruments. Reduction in batch failures, batch hold ups and generation of waste.

Position: Officer / Sr. Officer - Peptide Plant Grade: G12C / G12B No. of Position: 4 No. Job Location: Ahmednagar Qualification: M. Sc. (Organic Chemistry) Experience: 5 to 7 yrs experience in Peptide manufacturing plant Job Profile To issue and receipt of raw materials for manufacturing of Peptide Products as per requirement. Charging of batches and carry out all operations related to process as per BMR and written procedures. To manufacture peptide products as per BMR and written procedures in Peptide plant Operations, Calibration, Cleaning and Maintenance of process equipment and recording their usage logs. Monitor Process and cleaning turn around time (TR) during synthesis and purification of Peptide products. Monitor process parameter and yield. Reduction in Solvent usage and reduction in down time of the instruments. Reduction in batch failures, batch hold ups and generation of waste.

Position: Sr Executive / Manager Engineering - Mechanical Grade: G11B / G11A No. of Position: 1 No. Job Location: Ahmednagar Qualification: B. E. (Mechanical) Experience: 8 to 10 yrs experience in Engineering (Mechanical) of API manufacturing plant Job Profile Daily review of shift report and utility logbooks Allocation of work to sub-ordinators and contractors as per priorities. Ensure efficiently supply of utilities as per production requirement Ensure safety and statutory compliances of departmental activities Execution of preventive maintenance of equipment s as per schedule and updation of record in system. Spares management system. Timely availability of all critical spares. Attending the major breakdowns and preventive maintenance and set rights properly Maintaining the records like history cards, protocols, IMS & cGMP records. Execution of planned modification work. Preparation of documents of new equipment like protocol, history card, P. M. Schedule etc. Effective implementation of energy conservation activity. Training to sub-ordinates for cGMP safety, process critical parameters. Ensure proper housekeeping, cleaning of the department. Audit preparation as per cGMP requirement.