To maintain equipment in wet mixing, heat processing, homogenization & CIP as per schedule in the plant facility. Should have knowledge of food process industry and cGMP affecting product quality. Should have knowledge of EHS systems like work permits, LOTO etc. to perform the tasks safely Major Responsibilities: To comply with manufacturing & maintenance schedule. To maintain plant assets in line with quality & safety compliance. To build good work environment across teams to have healthy relations. To assume responsibility to improve process efficiency and quality of product. Responsible for maintaining automated Process Equipments in Process area Responsible for documentation of maintenance of records. Responsible for following policies, work instructions and SOP s. Responsible for ensuring continuous compliance to Good Manufacturing Procedures (cGMP) and maintaining the hygiene of his area/machine. Responsible for Troubleshooting and resolving operational & equipment issues. Responsible for following preventive maintenance plan and complete the tasks on time and perform the Work orders in Maximo. Need to involve in continuous improvement efforts /projects. Education: ITI/Diploma in related field (Mechanical, Electrical, Instrumentation) 3-4 years of relevant experience in Dairy, Food, Pharma and Chemical plant. Knowledge of processing equipments is must. Sound knowledge of cGMP. Background: Should have knowledge of food process industry and GMP affecting product quality Accountability & Scope: To maintain process equipments as per schedule in the plant facility. Should have knowledge of food process industry and cGMP affecting product quality. To maintain quality standards, tools and methods for processing materials into finished products.

To comply with manufacturing schedule To operate & monitor plant operation as per quality & safety compliance. To build good work environment across teams to have healthy relations. To assume responsibility to improve process efficiency and quality of product. Major Responsibilities Responsible for learning of operating and maintaining automated Process Equipments in Packing operation as per given specified area. Responsible to work under complete supervision in given specified area . Responsible for following policies, work instructions and SOP s Responsible for ensuring continuous compliance to Good Manufacturing Procedures (cGMP) and maintaining the hygiene of his area/machine. Responsible for Troubleshooting and resolving operational issues. Responsible for following and delivering batches as per upstream process requirements to ensure timely delivery to customers. To have in-depth understanding of packaging operations & Hygiene/GMP to provide the best output at shop floor & adhere to all compliances of food safety related concerns in Manufacturing department for maintaining food safety in plant. . Interpersonal skills in order to have healthy relationship with colleagues working in different teams at site. Communication skills in order to understand and provide necessary feedback or solutions within the Manufacturing team and internal customers. To learn knowledge about equipments & operate as per approved SOP & follow Hygiene/GMP to provide the best output at shop floor. Ensure self and team members consistently follow all EHS rules and procedures. Ensure self and team members immediately report any EHS incident and/or near misses (unsafe acts and conditions) promptly to supervision. Attend all required safety training and medical surveillance program requirements. Ensure self and team members wear all required PPE. Consistently take a leadership role in identifying team members who are and are not following procedures Complete required STOP observations Incur zero injuries of self and team members as a result of unsafe action/behavior or failure to follow established procedures or guidelines. Identify and report to supervision opportunities to reduce energy and water use, waste generation within your work area Education & Background Diploma/ITI in related field (Mechanical, Electrical, Instrumentation, Production) 3-4 years of relevant experience in Dairy, Food, Pharma and Chemical plant. Knowledge of Packaging/Filling Operations/Food Processing is preferred. Sound knowledge of GMP

We are looking for a highly motivated Project Leader Drug Substance to manage early phase projects from DRF tox batches up to first-in-human API deliveries. In this role you will closely collaborate with CDMO s in India but also work together with colleagues from other Novartis internal functions and sites. You will be part of the chemical and analytical development team at our site in Genome Valley and report to the local team leader Major accountabilities: To work with teams in the field of synthetic API development to support: 1. development of synthetic strategies to enable fast and reliable deliveries of API s for early phase development in close collaboration with our external CDMO partners in India Establish interdisciplinary project plans and track agreed activities with our key external partners in India and our Novartis internal stakeholders Ensure quality, quantity and timelines in all assigned projects Manage internal and external resource planning and allocation for assigned projects Advise team members and work according to appropriate SOP s, GLP, GMP, HSE and Novartis guidelines Ensure high quality of registration documents to enable timely IND/IMPD submissions. Interact with authorities where appropriate. Interact/collaborate with research and/or other functions in Development to facilitate transfer of knowledge and deliveries of API. Drive project handover to our internal late phase development site Minimum requirements: PhD and preferably postdoc in synthetic organic chemistry >10 years experience as a project leader in the chemical CDMO sector with strong process chemistry background Proven track record of expertise in the field of chemical process research and development incl scale-up of chemical processes till clinical phases Dedicated, thoughtful and flexible team working skills Excellent knowledge of English (oral and written) is required Good knowledge of common software applications and affinity to digital tools a plus

Location(s): India City/Cities: Ahmedabad Travel Required: Relocation Provided: Job Posting End Date: March 30, 2025 Shift: Job Description Summary: Looking for associates to join a greenfield site who will be responsible for start-up and operation of highly automated plant. We are looking for people who are self-motivated and technically strong who want to learn and develop into a high performing operations team. We are looking for team players who can collaborate among themselves to achieve high performance goals and are willing to learn and adapt to fast changing manufacturing environment. The person is expected to own and drive the end-to-end process and continuously improve on plant metrics. The role offers high degree of autonomy and an opportunity to grow in a fast-paced company. List the duties in order of importance: Safety Drive a safe environment culture (Safety First) Leverage BBS and Near Miss reporting to drive a continuous improvement culture Identify and participate in the eradication of unsafe conditions to achieve Zero Accidents Perform Machine Safety Risk assessments of line / process Compliance to health and safety procedures Participate actively in Quality improvements to achieve zero defects Ensure and sustain process and quality in compliance with Coca-Cola standards (KORE) regulations and procedures Participate and support internal and external audits Ensure accurate record keeping Autonomous Maintenance Equipment Care- Maintain work environment and equipment to agreed 5S standard Cleaning, lubrication, inspection and adjustments tasks Execution of first line maintenance Lead and participate in continuous improvement initiatives Learn and adapt to new technologies, like robotics, AI, ML etc Participate actively in Problem solving Troubleshooting and solving technical problems Data analysis and problem-solving tools like fish bone, 5 Why, Kaizen etc Root cause analysis of issues Plant Operation Execution of process checks, efficient packaging material management, accurate data recording, maintaining high level of GMP Execute physical and system (ERP) movements of all materials Driving fork truck, cycle counting and inventory control Operate system tools to enable operations - like Ignition, MII etc Operational Excellence and Digitalization Train and equip with OE tools and certifications Utilize available data / reports for optimal decision making Demonstrate continuous improvement of plant metrics Required Qualification & Experience Experience of working in highly automated manufacturing facility Worked in a self-directed manufacturing environment Worked in food or Pharma industry 0-3 years Work experience Diploma Degree- Automation and Mechatronics Skills: Our Purpose and Growth Culture: We are taking deliberate action to nurture an inclusive culture that is grounded in our company purpose, to refresh the world and make a difference. We act with a growth mindset, take an expansive approach to what s possible and believe in continuous learning to improve our business and ourselves. We focus on four key behaviors - curious, empowered, inclusive and agile - and value how we work as much as what we achieve. We believe that our culture is one of the reasons our company continues to thrive after 130+ years. Visit Our Purpose and Vision to learn more about these behaviors and how you can bring them to life in your next role at Coca-Cola.

Role: Veeva QMS - Clinical Experience: 3+ years Location: Pan India Skills: Veeva Quality Management System (QMS) is part of Veeva Vault , a cloud-based suite designed to streamline quality and compliance processes in regulated industries like pharmaceuticals, biotech, and medical devices . Clinical Vault within the Veeva ecosystem specifically focuses on clinical trial documentation, compliance, and quality processes . Key Features of Veeva QMS - Clinical Vault End-to-End Quality & Compliance Management for clinical trials Audit Readiness with automated tracking and reporting Document & Data Integrity with version control and security Regulatory Compliance for GCP, GMP, and global standards Integration with Veeva Vault Suite for seamless trial management

Job Title Senior Developer / Lead Opcenter RD&L in Teamcenter Location Pune / Bangalore Experience 8+ years Notice period Immedtae Joiner to 15 Days Job Description We are seeking a Senior Developer / Lead with expertise in Opcenter Research, Development & Laboratory (RD&L) within Teamcenter . The ideal candidate will lead a small development team , drive technical specifications for Opcenter RD&L solutions, and ensure seamless integration with Teamcenter PLM to enhance R&D workflows, compliance tracking, and product lifecycle management. Key Responsibilities Lead & Mentor a small development team, ensuring best practices in software development and system integration. Define Technical Specifications and solution architectures around Opcenter RD&L. Develop & Customize Opcenter RD&L solutions, integrating with Teamcenter and enterprise PLM systems. Optimize System Performance by enhancing workflows, automation, and data structures. Integrate with Teamcenter PLM to streamline material, formulation, and regulatory processes. Collaborate with Stakeholders including business analysts, QA teams, and end-users to gather requirements and deliver high-quality solutions. Debug & Troubleshoot system issues, ensuring high availability and performance. Stay Updated with Siemens Teamcenter & Opcenter advancements and industry trends. Required Skills & Qualifications 8+ years of experience in software development with expertise in Opcenter RD&L and Teamcenter PLM . Prior experience as a Senior Developer or Technical Lead , managing a small team and defining technical solutions. Strong programming skills in C++, Java, or C# for Teamcenter & Opcenter customization. Expertise in BMIDE, ITK, SOA, and Active Workspace (AWC) customization . Hands-on experience with Opcenter RD&L modules , including formulation management, material management, and regulatory compliance. Strong understanding of PLM, MES, and digital manufacturing concepts . Proficiency in SQL databases , web services, and API integration. Knowledge of regulatory compliance frameworks (e.g., FDA, ISO, GMP) is a plus. Excellent problem-solving, communication, and leadership skills . Preferred Qualifications Experience with Teamcenter 13.x or newer versions . Hands-on experience with cloud deployments (AWS/Azure) and microservices. Familiarity with Scripting (Python, PowerShell) and DevOps practices Must have skills Opcenter RD&L Expertise, Teamcenter PLM Expertise, Programming Skills (C++, Java, or C#), Technical Solution Design, System Performance Optimization, Collaboration & Stakeholder Management, Debugging & Troubleshooting, Compliance Knowledge (FDA, ISO, GMP) Secondary Skills Cloud Deployment (AWS/Azure), Microservices Architecture, Scripting & Automation (Python, PowerShell), DevOps Practices (CI/CD), SQL & API Integration, Teamcenter 13.x+ Keywords Opcenter RD&L Configuration, Workflow Customization, Integration, Cloud Deployment, Teamcenter, C++, Java, or C#, BMIDE, ITK, SOA, and Active Workspace (AWC) customization.

Overall line responsibility from production to packaging Start / Stop the machine and utility equipment. Performs process setting & monitoring. Monitor Material control (weight distribution, regrind levels, watch tail lengths, etc.) Performs regular quality control throughout the shift and visual quality checks Check & monitor process parameters like machine cycle time, mold cooling water temperature, compressed air pressure, process temperatures. Weigh waste material/ lumps and record in daily production report Ensures goods are produced in correct quantity and in accordance with agreed specifications Correctly record the details of bottles packed (pallet no., batch no, Qty. etc.) in the production report Report any deviation in the m/c operation or product to senior immediately. Perform mold change/color changes as needed. Maintain mold spare and perform preventive maintenance of molds. Maintain good housekeeping in and around the machine and within department. Follow all Safety norms and maintain shop floor discipline strictly. Maintain GMP & 5s as defined by management. Toolbox is checked regularly for condition of tools and quantity, to be restored immediately if required. Other duties assigned by management. What makes you great Diploma / CIPET background preferred Minimum 2+ years of experience in EBM Knowledge MS Office (Word, Excel, Power point) Ability to work well with other departments What you can expect working with us

Candidate is having good material( PET) processing knowledge Candidate must have good knowledge of handling Husky preform moulding machine. Candidate must have good knowledge of Resin Dryer like Piovan and Plastic system. Candidates have the ability to work independently and as part of a team. Knowledge of systems Like 5S, GMP and GDP. The candidate has good interpersonal and communication skills. What makes you great Candidate having 2 - 4 years of Experience in PET Preforms moulding. Candidate with Diploma - Electrical, Mechanical and CIPET-DPT/PPT is preferred. Good communication skills with reasonable proficiency in English speaking & writing Candidates with manufacturing background are preferred. What you can expect working with us We facilitate a smooth start through individual and accurate training as well as professional guidance and support We offer you a challenging task with a high degree of personal responsibility in an international working environment Dynamic working style in a fast-growing region and a dynamic team.

Job Description To ensure all the products manufactured and distributed by the bottling operation conform to the specifications through assurance of processes from supply to consumer. The QAE supports the identification, planning, documentation, and management of the practices, activities and resources needed to meet quality goals and objectives in a manner that enables management to assess quality performance. Job Responsibilities Responsibility for all quality management, and quality assurance activities in the bottling operation. Responsibility for adherence to Company guidelines and requirements in the supply, manufacturing and distribution processes. Responsibility for the conformance to specifications of the finished goods leaving the plant. Responsibility to monitor, assess and improve process capabilities in the plant Responsibility for conducting the required tests on raw materials, packaging materials, WIP and finished product at the specified frequencies. Responsibility for availability and calibration of inspection and testing equipment and chemical reagents. Responsibility for process control of the final syrup, water treatment Responsibility for raw material, ingredient and product identification and traceability. Responsibility for the implementation of GMP in the plant. Responsibility to document, implement and monitor a quality assurance system in accordance with the KORE Requirements. - Commitment to Development Commitment to Excellence Teamwork Planning and Execution Influencing Knowledge of the Business Job Requirement Minimum Education: Post Graduate in Microbiology. Minimum Experience: 2 - 3 years in a Microbiology in beverage industry.

{ "@context": "http://schema.org", "@type": "JobPosting", "datePosted": "2025-03-21", "description": " Title: Customer Service Associate Job Purpose: To provide an enhanced level of customer services and operational support. Customer Services agent will deal with shipment specific and other service-related issues. Main Duties and Responsibilities: To monitor all shipments on a daily basis to ensure that shipments are collected and delivered within agreed time frames. Working with customers, internal external, on daily basis with the aim of developing an excellent working relationship. Working with patients to ensure that collection requirements are met and that they are kept informed at all times during the process to ensure visibility. Booking and processing booking requests within Marken’s internal database, generating and verifying shipping documentation where applicable. Liaise with all relevant departments within the Global and Domestic Marken network to ensure that all customer requirements are met. Working all Marken offices and Local Service Providers to ensure the logistics transfer is handled efficiently thus meeting desired turnaround times. Entering clinical trial sites into Marken’s internal database (where necessary). Answering and dealing with general telephone and e-mail requests from external customers and internal offices/agents. Preparing, verifying and distributing country specific project documentation. Filing and archiving where required. Attending customer meetings and teleconferences, when required. Requirements: Skilled in use of Microsoft Suite (Excel, Word and Outlook) Knowledgeable with computers Thorough understanding of Aviation/Airline networks Excellent communication skills and ability to influence others Excellent problem solving and prioritization skills essential Flexibility in working hours required. Weekend coverage required in Customer Services in some cases Marken is a wholly owned subsidiary of UPS and is a critical part of UPS Healthcare. Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production. Moving Our World Forward by Delivering What Matters. ", "hiringOrganization": "Marken", "employmentType": "Full-Time", "industry": "Customer Service", "identifier": "oDkFvfwR", "jobLocation": [ { "@type": "Place", "address": { "@type": "PostalAddress", "addressLocality": "Andheri East", "addressRegion": "Mumbai", "addressCountry": "India" } } ], "title": "Customer Service Associate", "baseSalary": { "@type": "MonetaryAmount", "currency": "", "value": { "@type": "QuantitativeValue", "minValue": "", "maxValue": "", "unitText": "" } } } Customer Service Associate Customer Service Andheri East, Mumbai Apply Description Title: Customer Service Associate Job Purpose: To provide an enhanced level of customer services and operational support. Customer Services agent will deal with shipment specific and other service-related issues. Main Duties and Responsibilities: To monitor all shipments on a daily basis to ensure that shipments are collected and delivered within agreed time frames. Working with customers, internal external, on daily basis with the aim of developing an excellent working relationship. Working with patients to ensure that collection requirements are met and that they are kept informed at all times during the process to ensure visibility. Booking and processing booking requests within Marken s internal database, generating and verifying shipping documentation where applicable. Liaise with all relevant departments within the Global and Domestic Marken network to ensure that all customer requirements are met. Working all Marken offices and Local Service Providers to ensure the logistics transfer is handled efficiently thus meeting desired turnaround times. Entering clinical trial sites into Marken s internal database (where necessary). Answering and dealing with general telephone and e-mail requests from external customers and internal offices/agents. Preparing, verifying and distributing country specific project documentation. Filing and archiving where required. Attending customer meetings and teleconferences, when required. Requirements: Skilled in use of Microsoft Suite (Excel, Word and Outlook) Knowledgeable with computers Thorough understanding of Aviation/Airline networks Excellent communication skills and ability to influence others Excellent problem solving and prioritization skills essential Flexibility in working hours required. Weekend coverage required in Customer Services in some cases Marken is a wholly owned subsidiary of UPS and is a critical part of UPS Healthcare. Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production. Moving Our World Forward by Delivering What Matters. Apply Apply Later Back to Current Openings Share lang: en_US Share LinkedIn Facebook Twitter Email Similar Jobs Customer Service Associate Customer Service Associate Customer Service Associate Customer Service Associate Customer Service Team Lead

Location(s): India City/Cities: Ahmedabad Travel Required: Relocation Provided: Job Posting End Date: March 30, 2025 Shift: Job Description Summary: Looking for associates to join a greenfield site who will be responsible for start-up and operation of highly automated plant. We are looking for people who are self-motivated and technically strong who want to learn and develop into a high performing operations team. We are looking for team players who can collaborate among themselves to achieve high performance goals and are willing to learn and adapt to fast changing manufacturing environment. The person is expected to own and drive the end-to-end process and continuously improve on plant metrics. The role offers high degree of autonomy and an opportunity to grow in a fast-paced company. List the duties in order of importance: Safety Drive a safe environment culture (Safety First) Leverage BBS and Near Miss reporting to drive a continuous improvement culture Identify and participate in the eradication of unsafe conditions to achieve Zero Accidents Perform Machine Safety Risk assessments of line / process Compliance to health and safety procedures Participate actively in Quality improvements to achieve zero defects Ensure and sustain process and quality in compliance with Coca-Cola standards (KORE) regulations and procedures Participate and support internal and external audits Ensure accurate record keeping Autonomous Maintenance Equipment Care- Maintain work environment and equipment to agreed 5S standard Cleaning, lubrication, inspection and adjustments tasks Execution of first line maintenance Lead and participate in continuous improvement initiatives Learn and adapt to new technologies, like robotics, AI, ML etc Participate actively in Problem solving Troubleshooting and solving technical problems Data analysis and problem-solving tools like fish bone, 5 Why, Kaizen etc Root cause analysis of issues Plant Operation Execution of process checks, efficient packaging material management, accurate data recording, maintaining high level of GMP Execute physical and system (ERP) movements of all materials Driving fork truck, cycle counting and inventory control Operate system tools to enable operations - like Ignition, MII etc Operational Excellence and Digitalization Train and equip with OE tools and certifications Utilize available data / reports for optimal decision making Demonstrate continuous improvement of plant metrics Qualification- Diploma with 7 to 13 years work experience Preferred Discipline- Automation and IC Experience of working in highly automated manufacturing facility Candidate should have extensive troubleshooting experience in an highly automated setup Worked in a self-directed manufacturing environment Worked in food or Pharma industry Skills: Our Purpose and Growth Culture: We are taking deliberate action to nurture an inclusive culture that is grounded in our company purpose, to refresh the world and make a difference. We act with a growth mindset, take an expansive approach to what s possible and believe in continuous learning to improve our business and ourselves. We focus on four key behaviors - curious, empowered, inclusive and agile - and value how we work as much as what we achieve. We believe that our culture is one of the reasons our company continues to thrive after 130+ years. Visit Our Purpose and Vision to learn more about these behaviors and how you can bring them to life in your next role at Coca-Cola.

Long Description Operations: 1. Daily Call Review and Handling Escalations (e. g. Difference between Dates of call logged, and Date of call resolved. Problem Reported and Solution Provided Appropriateness/Classification of Call category. ) 2. Operation Enhancement/ sustenance. To find the root cause for the breakdown and taking the CAPA for the same (e. g. Root Cause Analysis / Preventive Action Document. No. of RCA-CAPA closed). Compliance: 1. Backup / Restore Management and Related Activity (e. g. Observations/ Non-Compliance reported during audit). 2. Compliance for Instrument connected machines (e. g. No. of NC received during Internal/External Audit with reference to deletion of Data, Copying of Data etc. ). 3. Validation Documentation for GMP/GLP departments (e. g. Observations/ Non-Compliance reported during audit). Projects 1. Managing expansion and upcoming changes in Plant / Office (e. g. Number of Projects undertaken and implemented. No deviation from target implementation dates) 2. Participating in Project Roll-out initiated from HO (e. g. Number of Projects undertaken and implemented, no deviation from target implementation dates, no of users covered and time taken). Support 1. Handling PLC/ HPLC/ Instrument connected machines related Calls and coordinating with third Party Vendors (e. g. Equipment downtime, Internal Customer Feedback/ Time taken) 2. Support and operation call related to WMS/WnD/DAS/ PLC/ Other Instrument connected software s Competencies Result Orientation Collaboration Stakeholder Management Process Excellence Innovation & Creativity Developing Talent Strategic Agility Customer Centricity Education B. Tech in Information Technology Graduation in Instrumentation or Computer Science Work Experience 5 to 10 years

JOB RESPONSIBILITY Position/ Designation Executive Production Name of the Unit Aarti pharma labs lab E-50 Name of the Plant/Department Production Block-01 Position Reports to Manager Production Experience 5 years ( Reputed API like Sun, cipla, lupin etc) Qualification Bsc / Msc CTC 5.00 Lacs Major Areas responsibilities Executive Production is responsible for process parameters as per standard and yield and quality maintained during manufacturing , as per production plan , Raw material , packing material indent to stores. Documentation indent to QA and execution in plant. BPR review and submit to QA, daily, monthly verification records. Monthly stock statement I st day of month and Raw material, solvent reconciliation in the II nd day of month. General material requisition monitoring/authorizing and housekeeping inside in manufacturing block. To ensure no shortcut is used in Process. In addition to handling incoming and outgoing communication, executive might be in charge of scheduling meetings, document review and preparation and possibly overseeing other staff. To encourage and motivate to subordinate with respect to discipline and safety and look after every activities/operations in plant by safety point of view to prevent any major or minor incident/accident. Detailed areas of this position Management Leadership and commitment Preparation of production department SOP and changes if required , review. Preparation of flow chart - housekeeping (5S) programme and implement it Housekeeping inside in manufacturing block. All regulatory document review and submit to QA . To plan and conduct process development batches as per technology transfer document. Solid waste, Bi- product recovered material , Crude Solvents transfer to stores. HSE and maintain record. Analyze process deviation / equipment which is affecting on yield and quality. In addition to handling incoming and outgoing communication, executive assistants might be in charge of scheduling meetings, document review and preparation and possibly overseeing other staff. Human Resource Management Internal Communication Co- ordination between Production , Store, Administrator, Quality control, Quality assurance and Maintenance. To trained the sub - ordinates. To take Tool box meeting and safety awareness To report production status and safety status of the plants to Production Manager / Head . Internal communications with plant in-charge, shift in- charge and officers to smooth operations or functions of plant activities to achieve the production target. Training To identify training need of all employees with the help of concerned HOD To assess the training need gaps’ of individual employee in consultation with concerned HOD To give training to concerned employees on handling of hazardous, toxic and flammable materials. to give training to all concerned employees on Material Safety Data Sheet. To conduct all training with feed back and assessment system. Linkages within/outside the organization Internal and External Customer Other Plants Internal and External Vendors Maintenance QC HR Admin Safety IT Process and Projects People management Ensure that the work force is highly motivated and aligned to the Company objectives. Ensure clear role clarity for everyone in the department. Ensure training and development of people ensuring career growth. Skills/Attributes Knowledge Qualification Experience Orientation (Interest) Training Communication Discipline Initiation Innovation Knowledge Process Chemistry and MSDS of applicable products (RM/FG/Packing etc) HAZOP Study SOP preparation Accident/ Incident Control Techniques Industrial HygieneRole & responsibilities Preferred candidate profile Perks and benefits

Dear Candidate, Greetings from Torrent Pharma !!! We are having an urgent opening for the position of Executive - Microbiology and details of the same are as under. Designation - Executive Department - QC (Microbiology) Qualification - M.Sc. / B.Sc. - (Microbiology / Biotechnology) Job Location - Indrad ( Ahmedabad - Mehsana Highway) Key Skills - Microbiological Testing, BET, MLT, Environmental Monitoring etc. Interested candidates can apply with their updated cv. Regards, Team HR

Production Department: Assisting in the operation of machinery and equipment as per SOPs. Helping in the batch manufacturing process under supervision. Following cGMP (current Good Manufacturing Practices) guidelines. Maintaining cleanliness (Good Housekeeping) in the production area. Recording batch manufacturing details accurately in logbooks. Supporting preventive maintenance activities. Ensuring proper handling of raw materials and finished goods. Quality Assurance (QA) Department: Assisting in review of batch records and documentation. Supporting deviation, change control, and CAPA tracking. Participating in internal audits and self-inspections. Learning about regulatory compliance and documentation practices. Preferred candidate profile B.Pharmacy / M. Pharmacy Fresher Perks and benefits Candidates with B. Pharmacy qualification will receive 11,000/- per month, Candidates with M. Pharmacy qualification will receive 12,000/- per month.

Knowledge of Protein Purification Experience of techniques and equipment handling involved in protein purification. Knowledge of GMP standards, SOPs quality management systems Awareness of QMS as per ISO13485: 2016 and ISO 9001:2015 standards.

Job Description Title: Micro Lead API Location: Ahmednagar Grade: G9B- Sr. Manager 2 JOB RESPONSIBILITIES To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media / reagents / culture / lysate / CSE / LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipments during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading )

Analysis of API/ excipients finished product and in-process samples with peer review. Method Development Calibration and maintenance of analytical instruments General lab responsibilities as decided by HOD. Following in-house compliance system Maintain hygienic condition in respective department. Follow GxP (GMP, GDP, and GLP) for all processes. Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements. All projects TRF management, segregation, and entry. Working standard/ impurities management Ensure data integrity. M. Sc. /M. Pharm

Ensure all the computerized systems meeting the 21 CFR Part 11, EU ANNEX 11and GAMP5 guidelines requirements. Perform, review & approve computerized system validation life cycle deliverables. Responsible for implementation and compliance of data integrity at site as DICO (Data Integrity Compliance officer). Implement regimen of Data integrity checks on shopfloor and updating of Data Integrity Risk Assessment (DIRA). Responsible for handling and compliance of SOPs related to Data Integrity & IT systems. Review / conduct of investigations related to Data integrity, Computerized Systems, and engineering department as applicable. Coordination for data integrity and IT-systems projects with stakeholders at site and corporate as well. Handling & Participation in internal & Data Integrity audits, its compliance. Involve in selection of Data Integrity (DI) champions & Impart necessary trainings to the DI champions Review of Change controls, Deviations, CAPA and other QMS tools. Review of Periodic review reports. Participated in supplier assessment for Computerized Systems, instruments & equipments etc. Review approve the schedules of data back-up & restoration, time synchronization etc. Audit trail reports review of computerized systems i. e. HMI, SCADA, DCS, etc. Review and ensure the compliance of user management activities of Computerized Systems. Preparation / review of the quality risk assessments i. e. part 11 compliance, data integrity etc. Review the Qualification documents of the manufacturing equipments, facility, utilities and associated ancillary systems. CAPA effectiveness verification. GMP compliance verification for the manufacturing equipment area, utilities and testing instruments. Review of software application qualifications. Comply with SHE Guidelines, SHE Rules and Regulations. Comply with usage of PPE wherever applicable. Observe unsafe acts and conditions and take corrective & preventive actions immediately, as necessary. Report any incident/accident/near miss/illness to the superiors. Follow companys quality procedures, standards, and specifications. Post Graduate / Graduate with relevant CSV experience

This individual will join a rapidly growing company that prides itself on offering Generic and Biosimilar brands all over the world, focused on the development of existing and new packaging products, aligned with the Sandoz objectives Job Description Your Key Responsibilities: Your responsibilities include, but not limited to: Work with a multinational team to create & develop new Packaging formats. From scratch to definitive technical specs Initiate and implement packaging projects that are aligned with Sandoz objectives To proactively work with suppliers to ensure packaging performance, also preventing and managing technical issues on existing packaging solutions To support Product Managers, Sites, Quality and Regulatory with the management of Packaging suppliers Identify optimization projects. Develop and implement global plans to achieve packaging KPIs such as the percentage of recycled content, eco-design, bioplastics to adhere to future regulatory environments He/she has expertise in Shipping Verification procedures . Indispensable great knowledge of creation/update of SOPs Excellent knowledge of Microsoft Office, Artioscad, Capepack, etc Valuable knowledge and lab equipment and use of it Willing to travel What you ll bring to the role: Essential Requirements: Holds an University degree in Packaging Technology (or equivalent) Brings a minimum of 10 years of experience in developing Pharma packaging solutions Solid experience in all packaging materials mainly thermo-forming, flexible laminates, glass, injection molding and carton

The Purpose of the Specialist role is having expertise in Extractables and Leachables assessment, and work in close collaboration with multiple functions such as MS&T, Supplier management, Regulatory, Toxicology, Procurement, Quality and Production. The individual plays a key role in support of Extractable and Leachable activities with a strong focus on data collection, Risk rating, assessments and evaluation. Job Description Your Key Responsibilities: Your responsibilities include, but not limited to: Understanding of Extractable and Leachable (E&L) risk assessment for materials based on supplier information and the ability to determine the risk level and update the Risk assessment. Building a comprehensive material library backed by corresponding E&L test data. Managing the coordination for Extractables studies or product-specific leachable studies. Preparation of E&L Risk assessment, E&L testing Protocol and Report. Compile E&L data and provide the information to Toxicologist for assessment. Proficient in risk evaluation, decision matrix, Gap Analysis, and outcome understanding manufacturing materials. Comprehensive knowledge of the chemical and physical properties (leaching tendency) of MOC materials. Skilled in defining the Original risk level, Mitigation factor, and Final risk level as part of the Risk Assessment process. Expertise in Extractable studies, their methodologies, analytical strategies, and design Expertise in setting the AET (Analytical Evaluation Threshold) and SCT (Safety concern threshold) for extractables and leachables detected during testing. Detailed understanding of E&L guidelines (SOPs, Pharmacopoeia and ICH standards, USP 665 & USP 1665 ) Proficient in identifying and assessing the Worst-case material representative approach. Collect the material list and data information from development centres and manufacturing sites. Active participation in E&L taskforce and network meetings. Also responsible for coordinating with the development, Supply management, QC, and Production department. What you ll bring to the role: Essential Requirements: Preparation of process and cleaning validation documentation (Protocols, reports) as well as change evaluations for new product launches and Life cycle management activities. Ensure project tracking documentation/tools are updated according to plan Collaborate closely with the development organization (or sending site) for technical transfers and new product launches to ensure knowledge transfer, appropriate control strategies, risk analysis and control, and readiness for commercial process validation Ensure that data integrity checks are conducted to verify that all the data is complete, consistent, and free from errors before proceeding with any further analysis or reporting Coordination of documentation review with the site MS&T, QA, and QC, also Reg CMC where applicable Preparation, approval and life cycle management of Gxp documents Experience: Bachelors degree in pharmacy, Pharmaceutical Technology, Chemical Engineering, Biotechnology, Chemistry, or equivalent science streams. Desirable MSc/MS. or equivalent experience. Min 8 years of experience in MS&T or in the manufacturing of pharmaceutical Drug substance and Product for Small and Large molecules. Should be familiar with regulatory guidance on ICH Q3,Validation, Product filing and Post approval changes. Proven project management experience in a cross-functional environment (e.g. multi-site, technical development, other functions). Expertise in reviewing and writing technical reports Good communication, Presentation and Interpersonal skills. Proficiency in English (oral and written) is required.

We are looking for a highly motivated Project Leader Drug Substance to manage early phase projects from DRF tox batches up to first-in-human API deliveries. In this role you will closely collaborate with CDMO s in India but also work together with colleagues from other Novartis internal functions and sites. You will be part of the chemical and analytical development team at our site in Genome Valley and report to the local team leader Job Description Major accountabilities: To work with teams in the field of synthetic API development to support: 1. development of synthetic strategies to enable fast and reliable deliveries of API s for early phase development in close collaboration with our external CDMO partners in India Establish interdisciplinary project plans and track agreed activities with our key external partners in India and our Novartis internal stakeholders Ensure quality, quantity and timelines in all assigned projects Manage internal and external resource planning and allocation for assigned projects Advise team members and work according to appropriate SOP s, GLP, GMP, HSE and Novartis guidelines Ensure high quality of registration documents to enable timely IND/IMPD submissions. Interact with authorities where appropriate. Interact/collaborate with research and/or other functions in Development to facilitate transfer of knowledge and deliveries of API. Drive project handover to our internal late phase development site Minimum requirements: PhD and preferably postdoc in synthetic organic chemistry >10 years experience as a project leader in the chemical CDMO sector with strong process chemistry background Proven track record of expertise in the field of chemical process research and development incl scale-up of chemical processes till clinical phases Dedicated, thoughtful and flexible team working skills Excellent knowledge of English (oral and written) is required Good knowledge of common software applications and affinity to digital tools a plus

Career County is looking for LEGAL EXECUTIVE to join our dynamic team and embark on a rewarding career journey. Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Candidate should have Pharma API company background Handling And Responsibility Of QMS Documents Change Control Deviation Out of Specification Market Complaint Corrective and Preventive Action (CAPA) Document Controls All document Issuance & Retrieval COA preparation BMR & BPR Preparation & Review Specification, Method of Analysis & Protocol & Report preparation for Finished product, Intermediate product, In-process, Raw material, Packing material. Standard Operating Procedure (SOP) Preparation Customer Query Related work/investigation. Policies & system procedures preparation. Training Calendar preparation and control. Qualification / Calibration / Validation Responsible for all Calibration activity Internal & External and maintained the record. Responsible for Equipment Qualification & Documentation control Vendor Qualification and regular follow up for updated documentation by the supplier Perks and benefits Transportation Leave enashment Health Insurance

DAMSUN INDIA PRIVATE LIMITED is looking for Quality Executive to join our dynamic team and embark on a rewarding career journey. Understand customer needs and requirements to develop effective quality control processes Devise and review specifications for products or processes Set requirements for raw material or intermediate products for suppliers and monitor their compliance Ensure adherence to health and safety guidelines as well as legal obligations Supervise inspectors, technicians and other staff and provide guidance and feedback Oversee all product development procedures to identify deviations from quality standards Inspect final output and compare properties to requirements Approve the right products or reject defectives Keep accurate documentation and perform statistical analysis Solicit feedback from customers to assess whether their requirements are met Submit detailed reports to appropriate executives Be on the lookout for opportunities for improvement and develop new efficient procedures