94 Urs Jobs

Required Experience: Minimum of 9-12 years in mainframe environments, focusing on platform consulting, modernization, or similar roles. Responsibilities: Provide application optimization support for the applications developed using IBM mainframe technology Stack JCL, COBOL, DB2, CICS and VSAM and IDMS. Strong analytical and problem-solving abilities for IBM mainframe. Deep understanding of mainframe architecture and modernization techniques. Analyze mainframe system level operations and suggest performance improvements. Proven experience with IBM ADDI or similar reverse engineering tools. Familiarity with IWS (IBM Workload Scheduler) and experience in reporting tool implementation. Experience with IDMS migrations, SCM tool transitions. Very good knowledge of tools like Omegamon, TWS. Expertise in system analysis, reverse engineering, and solution design for mainframe technology. Ability to assess and select suitable technological solutions. Analyze performance and system reports to provide improvement ideas. Coordinate with application development / support team as required. Coordinate with infrastructure support team if needed. Develop comprehensive architectural models and technical specifications. Should be aware of emerging trends in mainframe technology and modernization practices. The Role Offers: A challenging and rewarding role with opportunities to work on cutting-edge mainframe optimization projects. Professional growth through advanced training and career development programs. Collaborative and dynamic work environment with flexible work arrangements. Essential Skills: Strong analytical and problem-solving abilities specific to IBM mainframe environments. Expertise in system analysis, reverse engineering, and solution design for mainframe technology. Familiarity with emerging trends in mainframe technology and modernization practices. Experience in reporting tool implementation and use of IWS. Knowledge of additional reverse engineering tools or methodologies. Essential Qualification: Bachelors degree in Computer Science Engineering, or a related field.

What Youll Do? * Craft engaging promotional edits for web series, short-form content, trailers, teasers, and branded content that captivate and convert. * Work closely with promo writers, directors, motion graphic designers, and marketing teams to shape cohesive promo content. * Ensure visual identity, tone, and messaging align with the creative vision and platform expectations. * Select the right music, sound effects, and transitions to elevate storytelling and emotional impact. * Take feedback constructively and deliver multiple versions quickly with refinements based on performance.Who You Are * Degree or diploma in Film Editing, Mass Communication, Multimedia, or related fields. * Proficient in tools such as Adobe Premiere Pro, Final Cut Pro, After Effects (bonus), and basic color correction and sound balancing. * 710 years in promo/video editing for entertainment, digital media, television, or marketing agencies especially in Hindi content. * Comfortable working under tight deadlines and shifting priorities in a dynamic content environment. * Deep understanding of Indian audiences, regional nuances, and content consumption behavior.

Responsibilities 1. Preparation of PFD, URS, FDS, Cycle Time Analysis etc. 2. Calculation for Utilities, Peak Loads, Pipe / Pump sizing, Equipment capacity, and other accessories capacity/load/size 3. Preparation of P&ID, TS, DS, BOQ, Tender, Validation documents (VMP, FAT, IQ, OQ, PQ etc). 4. Desired exposure/ hands-on experience include: • Engineering & Consultancy Biotech & Pharmaceuticals • Process Engineers Sterile API / Formulations / Biotech Facilities • QA (Validation Experts) – Sterile API / Formulations / Biotech Facilities

Job Description Business: Piramal Critical Care Department: Information Technology Location: Kurla Travel: Low Job Overview To perform and document Computer System Validation of GxP Systems as per defined processes at Central Partner Functions and across Piramal Critical Care sites. Key Stakeholders: Internal Business Site / Central Partner functions IT Team (e.g. SAP / Infra / Quality IT / Allied / SAP etc) Key Stakeholders: External IT Vendors, IT Contractors/Consultants, Piramal CSV Partner Reporting Structure Reports to: AGM IT - CSV Education Qualification & Experience Graduate in Science/Pharmacy/Engineering Post Graduation MPharm/Science/MBA (Desirable) Candidate with 10-14 years of experience in Pharma/Life science domain working on CSV, Part 11/Annex 11, Data Integrity Work experience in Pharma or IT Sector will be desirable Roles & Responsibilities Must have thorough understanding, practical approaches for Computer system validation (CSV) & Computer Software Assurance of enterprise level applications. Accountable to ensure compliance of CSV documentation during various phases (project, operational & retirement) of software lifecycle (SLC).Well aware with GAMP5, CFR Part 11/EU Annex 11 and Data integrity requirements. To create end to end CSV deliverables for IT projects e.g. URS, FRS, CS, IQ, OQ, PQ, RTM, VSR, Risk assessment, etc. To create QMS documents e.g. Change control/Deviation/Incidents-Discrepancy/User access forms. To perform Root cause analysis and define CAPA based on QMS documents review. To support Quality Automations Initiatives across the Central Partner functions/PCC/PPL sites. To liaise with Site IT , Business SPOCs for CSV activities and IT Compliance initiatives. To guide and train IT & CSV teams (Central Partner Functions & Site) for CSV, and CSV Regulatory Compliance activities. To work along with Business, IT, QeC & Project Manager to ensure project timelines are met. Experience on validation of any of the enterprise level applications. e.g. Track wise, Ensur/Documentum, Paperless Validation Tools, LIMS, LMS, SAP, RIMS Applications, Artwork management Systems, Serialization, Veeva etc. Author, review and approval of SOPs, Guidelines/Policies as applicable. Competencies Good knowledge of 21 CFR Part 11 / Annexure 11 (Must) Good knowledge of CSV, CSA,GAMP 5 Guidelines (Must) Good knowledge of Data Integrity requirements for Pharma (Must) Experience in working with various geographical Location Stakeholders such as US, European, APAC. (Must) Experience of working with Global Pharma Cross functional Sites QC, QA, Manufacturing, IT, SAP etc. (Plus) Experience of validation on automation/digitization projects (Plus) Good Verbal and Written communication skills (Must) Aware of industry best practices and knowledge about Pharma 4.0 (Plus) Functional knowledge of CSV Regulatory guidelines, Quality Control and Manufacturing processes (Plus) Knowledge of IT systems and ITIL processes (e.g. Backup/Restoration, Infrastructure qualification, User access Management, etc.) About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders. PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators. Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space. Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment. Show more Show less

Roles and Responsibilities SME Level Expertise , Product level knowledge on Genesys OnPrem// Amazon Connect Innovation mindset Provide support for P1 and P2 issues Communication and Outage Management Work with Optum SMEs and Developers to identify and fix the issues identified in P1 and P2 tickets Work with L2 resources to get the RCA for P1 and P2 issues Update KT for any new Issues and set up process to proactive alert and fix for issues Mentor L1 and L2 team for any issues that they need help and guidance Identify any potential issues in platform and propose the fix/solution with team. Monitor the Changes scheduled and look for any potential impact which could be caused. Monitor the new Hotfix and Release of Genesys products and recommend the upgrade Automation Tools Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so Qualification Required : Genesys Level 3 Production support Good Understanding and Troubleshooting Skills set On following Genesys on Prem AreasSIP Server experience Orchestration server experience Rules Engine and GRAT experience Functionality and Troubleshooting Areas SIP Cluster, SIP ORS, URS, Composer, SCXML WWE, WDE- CHAT, GMS- GRE, GRAT- Knowledge on Splunk for Alerting & Monitoring. Amazon Connect AWS , Lambda , Mongodb, Chime, Cloudwatch, Event Bridge, Splunk, Grafana, Desktop AWS Connect expert Should have below Experience with Telephony and VOIP (Voice Over IP) & Contact Center Technologies Experience of CCaaS enterprise experience building Amazon Connect contact flows integrated with Python, Lambda and JSON & applications using AWS services (Cloud Watch, Kinesis, S3, Lex, Poly) Hands-on development experience with cognitive service such as Amazon connect, Amazon Lex, Lambda, Kinesis, Athena, Pinpoint, Comprehend, Transcribe

About The Role We are seeking a skilled and experienced MES Engineer with hands-on expertise inKrber Werum PAS-Xto support manufacturing operations in a regulated pharmaceutical or life sciences environment. The ideal candidate will have a strong technical foundation, validation knowledge, and excellent communication skills to effectively bridge the gap between technical teams and business stakeholders. Key Responsibilities:- MBR Design & Development: Design and create complex Master Batch Records (MBRs) for Weighing & Dispensing, Manufacturing, and Packaging processes. Analyze site-specific requirements and translate them into functional MBRs. Validate MBRs for deployment across manufacturing sites. System Configuration & Administration: Configure and customize Werum PAS-X modules including GMBRs, PVL, PMBRs, Equipment Management, Material Flow, Weigh & Dispense, EBR, and Master Data. Design and developState Diagramsand determine updates forMaster DataandEquipment Management. Integration & Interface Management: Work on SAP-MES interfaces, Level 2 (L2) integrations, and report development. Ensure seamless data flow and system interoperability. Compliance & Validation: Ensure compliance with GxP, GAMP, and 21 CFR Part 11 standards. Participate in validation activities includingIQ/OQ/PQand documentation. Project & Stakeholder Management: Act as an Offshore Lead and manage service delivery for PAS-X. Liaise with clients and stakeholders to gather requirements and provide technical solutions. Provide support forWerum PAS-X installation, upgrade, development, and configuration. Primary Skills (Must-Have): Strong hands-on experience withWerum PAS-X(Specification, Execution, Compliance & Performance Modules). Expertise inMBR creation,State Diagram design, andMaster Data configuration. Experience inPAS-X System Administrationandcustomization. Knowledge ofISA-95/S88 standardsand their application in MES design. Familiarity withSAP-MES integrationandL2 automation systems. Understanding ofpharmaceutical manufacturing processesand regulatory requirements. Secondary Skills (Good-to-Have): Programming knowledge inSQL,C#, andJava. Experience withuser management,system profile creation, andreporting tools. Exposure toITIL frameworksandIT service management. Experience inproject management,client communication, andteam leadership. IT Skills: SQL Queries C# (C-Sharp) Java Experience in: User management System profile creation System configuration and troubleshooting

Dear Applicants, Job Opportunity: " Urologist" We are delighted to announce excellent career opportunities for both freshers and experienced professionals in Urology . Join reputed Super-speciality Hospitals, Multi-speciality Hospitals, and Diagnostic Centres across India. What We Offer: Attractive Salary Package Performance-based Incentives Accommodation Facilities Job Title: Urologist Consultant Qualifications: MBBS- MS/MD/DNB/MCH Package: Upt o - (65 LPA) Location: Gujarat - Rajula Karnataka - Sindhanur Madhya Pradesh - Sagar Maharashtra - Nanded Rajasthan - Bhilwara Uttar Pradesh - Moradabad Uttarakhand - Kashipur Position Type: Full-Time Preferred Skills: . Familiarity with electronic health record (EHR) systems. - Urology, Endourology, Transurethral Resection of the Prostate (TURP), Prostate Biopsy, Kidney Stone, Lithotripsy, Percutaneous Nephrolithotomy (PCNL), Urinary Tract Infection, Benign Prostatic Hyperplasia (BPH), Erectile Dysfunction, Male Infertility, Bladder Cancer, Prostate Cancer, Renal Cancer, Urethral Stricture, Urinary Incontinence, Urinary Catheterization, Ultrasound, CT Urography, MRI, EMR for Urology, EHR, Uroflowmetry, Cystoscopy, URS, RIRS, ESWL, Ureteroscopy, Nephrectomy, Pyeloplasty, Urethroplasty, Urodynamics, Uro-oncology, Andrology, Laparoscopic Urology, Robotic Surgery, Renal Transplant, Prostate, Bladder Tumor, Varicocelectomy, Penile Prosthesis, Testicular, Urethral Dilatation, Stent Placement, Suprapubic Catheterization, Reconstructive Urology, Urological Imaging, TRUS, Stone Disease, Minimally Invasive Surgery Benefits: Opportunities for professional development and continuing education. Supportive and collaborative work environment. How to Apply: Interested candidates should submit their resume and a cover letter to Mail ID- jobs@angplacement.in Thanks & Regards, Jagdish Teli Managing Director 7000476894 ANG Placement & Staffing Solutions Pvt Ltd.

Dear Applicants, Job Opportunity: " Urologist" We are delighted to announce excellent career opportunities for both freshers and experienced professionals in Urology . Join reputed Super-speciality Hospitals, Multi-speciality Hospitals, and Diagnostic Centres across India. What We Offer: Attractive Salary Package Performance-based Incentives Accommodation Facilities Job Title: Urologist Consultant Qualifications: MBBS- MS/MD/DNB/MCH Package: Upt o - (65 LPA) Location: Gujarat - Rajula Karnataka - Sindhanur Madhya Pradesh - Sagar Maharashtra - Nanded Rajasthan - Bhilwara Uttar Pradesh - Moradabad Uttarakhand - Kashipur Position Type: Full-Time Preferred Skills: . Familiarity with electronic health record (EHR) systems. - Urology, Endourology, Transurethral Resection of the Prostate (TURP), Prostate Biopsy, Kidney Stone, Lithotripsy, Percutaneous Nephrolithotomy (PCNL), Urinary Tract Infection, Benign Prostatic Hyperplasia (BPH), Erectile Dysfunction, Male Infertility, Bladder Cancer, Prostate Cancer, Renal Cancer, Urethral Stricture, Urinary Incontinence, Urinary Catheterization, Ultrasound, CT Urography, MRI, EMR for Urology, EHR, Uroflowmetry, Cystoscopy, URS, RIRS, ESWL, Ureteroscopy, Nephrectomy, Pyeloplasty, Urethroplasty, Urodynamics, Uro-oncology, Andrology, Laparoscopic Urology, Robotic Surgery, Renal Transplant, Prostate, Bladder Tumor, Varicocelectomy, Penile Prosthesis, Testicular, Urethral Dilatation, Stent Placement, Suprapubic Catheterization, Reconstructive Urology, Urological Imaging, TRUS, Stone Disease, Minimally Invasive Surgery Benefits: Opportunities for professional development and continuing education. Supportive and collaborative work environment. How to Apply: Interested candidates should submit their resume and a cover letter to Mail ID- jobs@angplacement.in Thanks & Regards, Jagdish Teli Managing Director 7000476894 ANG Placement & Staffing Solutions Pvt Ltd.

As an R&D Executive at PTC - MORAIYA, your primary responsibility will be characterizing materials and developing/qualifying packaging systems including primary, secondary, and tertiary packaging. You will be tasked with completing design control deliverables and ensuring compliance with relevant regulatory requirements for submission. Additionally, you will provide post-launch troubleshooting support for complex products and develop various drug delivery devices such as Pen Devices, Auto Injectors, DPI, and pMDI while maintaining a deep understanding of regulatory expectations. Your role will involve compiling essential documents such as User Requirement Specifications (URS) and design control/history files for combination products. You will be responsible for conducting functional performance studies of devices, coordinating with vendors to execute non-disclosure agreements, and finalizing trade dress. Furthermore, you will source new packaging materials, develop new vendors, track packaging material availability and procurement, and support cost evaluation processes. In this position, you will prepare lab notebooks, Packaging Development Reports, Bill of Materials (BOMs), and batch Packaging Records for various stages from engineering batches to commercial batches. You will also be involved in preparing specifications, standard test procedures for packaging material components, Standard Operating Procedures (SOPs), and guidelines. Troubleshooting issues related to the process and usage of packaging materials, conducting SAP-related activities, managing change control procedures, and responding to packaging-related queries from regulatory authorities will be part of your responsibilities. Moreover, you will design pack configurations for commercial launch based on marketing requirements, conduct transportation studies, revise artworks for Reference Listed Drug (RLD) changes, and optimize pack configurations to meet marketing needs, cost considerations, and automation requirements. Your role will require attention to detail, regulatory compliance, and effective communication with internal and external stakeholders to ensure the successful development and implementation of packaging systems.,

The role involves handling document issuance, distribution, and retrieval, including verification of various documents such as Batch Manufacturing records, Protocols, layouts, specifications, etc. Issuing approved Standard Formats and Logbooks to User Departments, as well as managing line-clearance checklists, interventions checklist, and BMR/BPR pages. Additionally, handling proposed changes per the change control procedure, assessing associated risks/impacts, and ensuring the implementation of action plans. Conducting investigations using root cause analysis tools, performing additional studies, and deriving appropriate CAPA. Managing recommended CAPA and evaluating the implementation of recommended actions. Performing trend analysis on deviations, change controls, complaints, etc., to identify repetitive events for further evaluation and CAPA. Reviewing URS, DQ, and vendor/supplier documents related to qualification. Preparing and reviewing Validation/Qualification protocols and reports. Executing and reviewing Qualification/Validation activities of Equipment/System/Facility and Plant utilities, coordinating with relevant departments for timely completion. Preparing and reviewing media fill and hold time protocols and reports, as well as Standard Operating Procedures for the Quality Assurance Department. Assessing Change Control, Deviation, CAPA, Investigations, and preparing protocols for process validation and cleaning verification/validation. Conducting sampling activities as per protocols and managing risk assessment activities related to equipment/process/facility/system. The ideal candidate should have a B.Sc/M.Sc/B.Pharm/M.Pharm degree.,

Job Description Project Engineer Position: Project Engineer Reporting to: Sr. Project Engineer Location: Pune (with client site visits as required) Job Type: Permanent Company Overview Beyzon Foodtek Pvt. Ltd., based in Pune, is a management and food processing technology consulting firm. We help food industry clients design best-in-class infrastructure, improve efficiency, and prepare for future challenges. Our services deliver significant improvements in manufacturing capacity, food safety, quality, and profitability. Position Overview The Project Engineer will play a key role in the execution of projects for food manufacturing companies. This role requires hands-on experience in project functions, particularly in utilities, equipment installation, commissioning, and process optimization. The candidate should be technically sound, detail-oriented, and capable of executing projects within defined timelines. Qualification & Experience Qualification: B.E. (Mechanical) Experience: Total 4–5 years of experience Prior experience in the FMCG Food Industry will be considered an added advantage. Exposure to manufacturing and project functions is essential. Hands-on knowledge in utilities installation, process equipment, packaging machines installation & commissioning. Key Responsibilities 1. Provide engineering support for projects, including Brownfield, Greenfield, manufacturing ramp-up, and technology adoption. 2. Assist in end-to-end project planning, coordination, execution, commissioning, and closure. 3. Conduct utilities mapping, planning, and studies of existing equipment/process lines to suggest improvements. 4. Prepare and maintain project management documentation, Gantt charts, and related reports. 5. Draft AutoCAD layouts for plant and equipment as required. 6. Coordinate with internal Food Technology staff, client teams, and vendors; provide regular updates on progress. 7. Collaborate with Food Technology Executives and client stakeholders to conduct equipment/process validation trials. 8. Liaise with equipment suppliers to collect technical and commercial information, support meetings, and documentation. 9. Participate in Factory Acceptance Tests (FAT), installation, commissioning, and validation of equipment/process lines. 10. Document FAT trials; prepare installation/commissioning reports, and Minutes of Meeting (MoM). 11. Prepare presentations and other project-related documentation. 12. Visit client sites (factories/project sites) as required for project activities. 13. Carry out any other project-related responsibilities assigned by seniors. Essentials Quick learner, self-starter, and strong team player. Proficiency in English verbal & written communication. AutoCAD knowledge/experience preferred. Computer savvy, well-mannered, composed personality.

Job Description Senior Project Engineer Position: Senior Project Engineer Reporting to: Company Directors Location: Pune (with frequent client site visits) Company Overview Beyzon Foodtek Pvt. Ltd., based in Pune, is a management and food processing technology consulting firm. We help food industry clients design best-in-class manufacturing setup, improve efficiency, and prepare for future challenges. Our services deliver significant improvements in manufacturing capacity, food safety, quality, and profitability. Role Overview As a Senior Project Engineer at Beyzon Foodtek Pvt. Ltd., you will lead project engineering activities, guide a team of project engineers, and ensure the timely, cost-effective, and quality-driven execution of diverse projects in the FMCG Food industry. These projects may include Brownfield/Greenfield projects, manufacturing capacity enhancement, and adoption of advanced manufacturing technologies. Experience & Qualifications Experience: 7–10 years of experience, with at least 4–5 years in core project management functions. Prior exposure to FMCG Food Industry projects will be an added advantage. Education: Bachelor’s degree in Mechanical Postgraduate qualifications in Project Management or allied areas will be a plus. Technical Skills: Strong knowledge of project planning and execution. Proficiency in AutoCAD Familiarity with utilities planning, equipment installation, commissioning, and validation processes. Soft Skills: Strong leadership, communication, vendor management, and documentation skills. Key Responsibilities 1. Lead and guide a team of project engineers in executing assigned projects. 2. Provide engineering support for diverse projects, including Brownfield, Greenfield, manufacturing ramp-up, and technology adoption. 3. Manage end-to-end project lifecycle: planning, coordination, execution, commissioning, and closure. 4. Conduct utilities mapping and planning as an integral part of every project. 5. Study existing manufacturing equipment, process lines, and utilities to recommend improvement interventions. 6. Ensure project execution adheres to approved engineering details, GFC drawings, timelines, and budgets. 7. Create AutoCAD drawings for plant and equipment layouts as required. 8. Coordinate with internal teams, client teams, and vendors; provide weekly project updates to directors. 9. Liaise with equipment suppliers to obtain technical and commercial information, conduct meetings, and finalize details. 10. Conduct equipment FAT (Factory Acceptance Tests) & Oversee equipment and process line installation and commissioning & Prepare reports for the same. 11. Visit client sites (factories or project sites) as required. Key Attributes Proven ability to lead projects from planning to closure. Strong problem-solving and decision-making skills. Ability to manage multiple stakeholders (internal teams, clients, vendors).

Designation Associate Manager to Sr. Manager Role Lead Automation Engineering Projects Department – Projects Reporting – Head Projects Experience – 12 to 15 Years Qualification – BE/B.Tech – Instrumentation/Electronics/Electrical Or related discipline Role Type – Individual Contributor Role - Lead Automation You are leading Automation centrally with our Engineering project team. In this position you will be a mentor and technical coach leading strategic transformation projects for the site. Therefore, your role is of significant importance and has high visibility within the Zydus Manufacturing Network. Your main responsibilities: Implementation of global automation standards including the development of site-specific automation concepts and solutions. Development of project plans, URS, FRS, and commissioning documents for new automated systems. Develop strategic initiatives and present best practices and key industry trends, including developing and delivering new and unique approaches to automation and digital. Develop, automate, and validate data management processes. Create support and maintain BI system and its infrastructure Responsibility for the optimization, standardization, and upgrade of existing automation technology and process control. Ensuring availability and a target-oriented flow of systems and processes. Responsible for the implementation and administration of the access and virus protection, including back-up and disaster recovery plans for the industrial automation systems. Your profile: Proven successful deployment of automation and digital projects such as AGV, AMR, MES, Track & Trace, equipment integration, computer vision, data automation (ETL), and implementation of BI systems Degree in automation engineering, electrical engineering, or technically comparable studies. Sound knowledge of process control systems and automation systems. Significant knowledge and experience in PLC and SCADA systems, network solutions and virtual environment. Good to have programming skills in software of Mitsubishi, Siemens etc. Fluent programming skills such as Python, SQL, and familiarity with data analysis and statistics. Sound experience in project management and in dealing with project planning methods and tools. Experience in defining, implementing, and managing work structures for the automation department. Leadership skills, a high sense of responsibility and strong communication skills, assertiveness, and team spirit.

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Genesys Cloud AI Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application development aligns with business objectives, overseeing project timelines, and facilitating communication among stakeholders to drive successful outcomes. You will also engage in problem-solving activities, providing guidance and support to your team while ensuring that best practices are followed throughout the development process. Roles & Responsibilities:- Collaborate and manage the team to perform.- Responsible for team decisions.- Engage with multiple teams and contribute on key decisions.- Provide solutions to problems for their immediate team and across multiple teams.- Facilitate training and development opportunities for team members to enhance their skills.- Monitor project progress and implement necessary adjustments to meet deadlines. Professional & Technical Skills: - Must To Have Skills: Proficiency in Genesys Cloud AI.- Strong understanding of cloud-based application architecture and deployment.- Experience with application design and development methodologies.- Ability to analyze and troubleshoot application issues effectively.- Familiarity with integration techniques for various software applications. Additional Information:- The candidate should have minimum 5 years of experience in Genesys Cloud AI.- This position is based at our Bengaluru office.- A 15 years full time education is required. Qualification 15 years full time education

Conducting regular patient check-ups and exams. Diagnosing and treating illnesses and disorders related to the urinary tract, kidneys, and male reproductive system. Prescribing medication and follow up instructions. Performing surgical procedures as needed. Maintaining accurate patient records and communicating with fellow healthcare professionals as needed. Interested candidate with relevant expereince of 2 to 4 years may apply or whatsapp .

Dear Applicants, Job Opportunity: " Urologist" We are delighted to announce excellent career opportunities for both freshers and experienced professionals in Urology . Join reputed Super-speciality Hospitals, Multi-speciality Hospitals, and Diagnostic Centres across India. What We Offer: Attractive Salary Package Performance-based Incentives Accommodation Facilities Job Title: Urologist Consultant Qualifications: MBBS- MS/MD/DNB/MCH Package: Upt o - (65 LPA) Location: Chhattisgarh - Raipur Gujarat - Rajula Karnataka - Sindhanur Madhya Pradesh - Sagar Maharashtra - Nanded Rajasthan - Bhilwara Uttar Pradesh - Moradabad Uttarakhand - Kashipur Position Type: Full-Time Preferred Skills: . Familiarity with electronic health record (EHR) systems. - Urology, Endourology, Transurethral Resection of the Prostate (TURP), Prostate Biopsy, Kidney Stone, Lithotripsy, Percutaneous Nephrolithotomy (PCNL), Urinary Tract Infection, Benign Prostatic Hyperplasia (BPH), Erectile Dysfunction, Male Infertility, Bladder Cancer, Prostate Cancer, Renal Cancer, Urethral Stricture, Urinary Incontinence, Urinary Catheterization, Ultrasound, CT Urography, MRI, EMR for Urology, EHR, Uroflowmetry, Cystoscopy, URS, RIRS, ESWL, Ureteroscopy, Nephrectomy, Pyeloplasty, Urethroplasty, Urodynamics, Uro-oncology, Andrology, Laparoscopic Urology, Robotic Surgery, Renal Transplant, Prostate, Bladder Tumor, Varicocelectomy, Penile Prosthesis, Testicular, Urethral Dilatation, Stent Placement, Suprapubic Catheterization, Reconstructive Urology, Urological Imaging, TRUS, Stone Disease, Minimally Invasive Surgery Benefits: Opportunities for professional development and continuing education. Supportive and collaborative work environment. How to Apply: Interested candidates should submit their resume and a cover letter to Mail ID- jobs@angplacement.in Thanks & Regards, Jagdish Teli Managing Director 7000476894 ANG Placement & Staffing Solutions Pvt Ltd.

You will be responsible for documentation and execution of qualification activities. This includes preparation, review, and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ (Requirement Qualification) documents. Your responsibilities include the review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems. You will be responsible for new project-related FAT (Factory Acceptance Test) and SAT (Site Acceptance Test). You will review and compile raw data, relevant certificates, analysis test reports, and preparation and review of the final summary report. Additionally, you will be responsible for preparation and review of protocols and reports for media fill validation and cleaning validation. Your role involves the initiation of relevant CRN (Change Request Number) for new or existing activity, timely closure of assigned action plans as per CRN, and CRN review and approval. You will also be responsible for corrective and Preventive Action (CAPA) implementation and handling incident investigations and CAPA related to qualification. As part of your role, you will prepare and review VMP (Validation Master Plan), conduct training for employees and external vendors as a qualified trainer, and prepare and review qualification SOPs (Standard Operating Procedure). You will conduct investigations as a site investigation team member and update the Qualification status label. You will be responsible for the periodic qualification schedule preparation, updating, and execution, as well as the qualification of new or transferred equipment. Additionally, you will provide necessary assistance and support to various regulatory, internal, and external inspections.,

• Implement and configure clinical trial solutions as per client requirements. • Collaborate with clients and internal teams for smooth project execution. • Provide training, documentation, and post-implementation support Required Candidate profile • 4+ years of IT solution implementation experience in Healthcare/Clinical Trials/Life Sciences. • Hands-on experience with CTMS, LIMS, EDC, or similar systems preferred. Perks and benefits - GPA &term Insurance-5 days week -Flexible timing

Job Title - (Genesys)+(Level 7-Manager)+(Entity -S&C GN) Management Level: 7-Manager Location: Gurgaon, Mumbai, Bangalore, Chennai, Pune, Hyderabad Must-have skills: Genesys, Genesys pure cloud, Genesys cloud Good to have skills: Genesys PureConnect, Genesys Engage, Consulting experience across any of the CCaaS/Customer Service solutions (Amazon Connect, Nice, Verint, Cisco, Five9, Sprinklr, Twilio, Salesforce, Servicenow, Adobe, Microsoft Azure, Google Cloud etc.) Job Summary : This role involves driving strategic initiatives, managing business transformations, and leveraging industry expertise to create value-driven solutions. Roles & Responsibilities: Develop and execute technology transformation strategies, oversee implementation projects, and optimize digital capabilities for business efficiency. You will work closely with our clients as consulting professionals who design, build and implement initiatives that can help enhance business performance. As part of these, you will Functional Experience :Develop and execute the contact center strategic initiatives including AI/Gen AI strategy to improve customer experience & optimize business expenses, operational costs Industry Experience Experience & Specialization in any of industry divisions such as Communication Media & Technology, Financial Services, Health & Public Services, Products & Resources. Understand market and customer challenges: Create business case and strategic transformation roadmap based on market trends. Help sell and deliver Genesys contact center solutions to clients: Product overview, Partner readiness support, pricing, documentation, first call presentations Drive Partner support activities: A strong focus on nurturing deeper, more strategic relationships with key parties Develop requirements based on leadership input: Performance/Status reporting, Problem Solving and Conflict Management Bring your best skills forward to excel at the role: Experience working with Customer Service Operations: Experience in Contact Center channels, leading Customer Service operations assessment/benchmarking, identifying gaps and deriving business case for driving improvements. Experience implementing multichannel self-service/IVR and Omni-Channel Orchestration Routing: Experience in Genesys Cloud/Engage suite. In-depth knowledge and know-how of Customer Service Operations: Cross-industry experience, functional and hands on experience on Voice and Non-Voice (SMS, Email, Chat etc.) applications solutioning using tools like Genesys Administrator & Architect/Composer/Designer. Proactively identifying customer needs through a technical benefits assessment: Carefully building the business value of the solution, to assist with overcoming potential objections to proposed technical solutions. Knowledge of on-premises, on-cloud, hybrid cloud and cloud economics: This includes pricing strategy of different Genesys on-premises and cloud solutions and providing detailed TCO Experience in Genesys Cloud administration & application experience: Use Genesys Architect/Composer/Designer, Genesys Framework Components (such as Edge, BYOC, SIP, GAX, GVP, AppFoundry, eServices, GRE, URS, Info Mart, GMS, OCS, GPlus Integrations etc.) or similar solutions. Professional & Technical Skills: - Relevant experience in the required domain. - Strong analytical, problem-solving, and communication skills. - Ability to work in a fast-paced, dynamic environment. Additional Information: - Opportunity to work on innovative projects. - Career growth and leadership exposure. About Our Company | Accenture Qualification Experience: 8+Years Educational Qualification: MBA from a tier 1 institute

As a Senior Engineer in Plant Engineering at Dr. Reddys Laboratories Ltd., you will play a crucial role in ensuring adherence to Operations & Maintenance SOPs, schedules, and compliances to prevent breakdowns. Your responsibilities will include the installation and qualification of equipment, preparation and execution of various protocols and reports, breakdown and preventive maintenance of a wide range of equipment, PR initiation and vendor management for AMC equipment. Additionally, you will be in charge of executing infrastructure projects related to electrical requirements, overseeing project activities for quality, delivery, timelines, and safety, and ensuring zero incidents through compliance with work permits and safety procedures. You will also be responsible for conducting safety audits, maintaining critical spares on-site, tracking maintenance-related expenditure and budgets, ensuring equipment availability for production, and maintaining human and equipment safety in daily operations. Moreover, you will be involved in the initiation and closure of Change Controls, CAPA, Incident Investigation, SOP creation and revision for Plant Engineering, and collaborating with cross-functional teams to implement sustainability projects. To qualify for this role, you should hold a Diploma or Bachelor's degree in Electrical, Instrumentation, or Mechanical Engineering, along with a minimum of 10 years of experience in Engineering and Projects, particularly in Biologics, Formulation, Biotech, Biosimilars, Cell, and Gene therapy manufacturing. Your technical skills should include proficiency in operations and maintenance of electrical/mechanical systems, expertise in overseeing infrastructure projects, and experience in navigating audits. In addition to your technical skills, you should possess strong behavioral skills such as the ability to lead and manage teams effectively, plan and coordinate projects, communicate effectively, and demonstrate a proactive inclination towards energy-saving initiatives. At Dr. Reddys, our work culture is centered around the belief that Good Health Cant Wait. We strive to empower individuals to lead healthier lives through innovative healthcare solutions, foster a culture of empathy and dynamism, and value individual ability while promoting teamwork and shared success. If you are looking to join a dynamic team that is committed to making a positive impact on healthcare, we encourage you to explore opportunities with us at Dr. Reddys Laboratories Ltd. For more information, please visit our career website at https://careers.drreddys.com/#!/.,

As a Business Analyst at DDi, you will play a crucial role in eliciting and documenting requirements using various techniques such as meetings and group discussions. You will be responsible for preparing User Requirement Specifications (URS) to capture all requirements and updating them based on review comments. Additionally, you will create Functional Requirement Specifications (FRS) with detailed functional requirements in alignment with the approved FRS template and update them as per review comments. You will collaborate with the development team to provide functional clarifications and perform functional testing to ensure that all requirements are implemented as per the documents. Conducting impact analysis in terms of functionality and dependency for each change request and documenting the impact will also be a key aspect of your role. Furthermore, you will update URS, FRS, and Requirements Traceability Matrix (RTM) to incorporate approved change requests. Participating in project closure activities to prepare or update project documents and lessons learned will be part of your responsibilities. You are expected to update the project status periodically or upon request. Moreover, you will be encouraged to propose innovative solutions using mocks and navigation documents. This role requires you to work independently without direct supervision and manage your time and workload effectively. DDi is a leading technology partner in the Life Sciences industry, offering innovative technology products and solutions for Clinical Development, Regulatory, and Safety domains. With a customer base ranging from global Top 100 life science companies to small and mid-size manufacturers, DDi, as a Makro Company, leverages a unique blend of functional and domain expertise to cater to the technology needs of clients worldwide.,

You will be part of a greenfield project located in GIDC Vapi, covering an area of 10,556 sq m dedicated to the manufacturing of Pharma Intermediates and APIs. The project is designed to include a main intermediate production building, a GMP facility, and infrastructure for Catalytic Hydrogenation, emphasizing sustainable practices and competitive innovation. Your responsibilities will involve the preparation and upkeep of Engineering/Project documentation, Qualification & Validation documents throughout the various stages of the greenfield project until commercial manufacturing. It is essential to ensure the implementation and adherence to industry/cGMP best practices. This includes creating Qualification documents such as URS, DQ, IQ, OQ & PQ for production and utility equipment, as well as overseeing Engineering documents encompassing certificates, calibration, test results, inspection requests, non-compliance reports, and other crucial QA/QC documents. You will be accountable for tasks like conducting factory acceptance tests at vendor sites, qualifying new equipment, and periodically re-qualifying equipment and facilities like PW plant HVAC. Additionally, you will be involved in the Preparation & Review of SOPs for the Engineering department, Training and Approval of Qualification SOPs, preparing Facility qualification documents, and developing Project-specific qualification plans for significant changes. Your role will also entail the creation of various documents such as Installation and operational qualification protocols and reports, Performance Qualification Protocols and reports, and conducting training sessions for new hires and Executives on Qualification Activities. To qualify for this role, you should hold a BE/ BTech degree in Chemical/Mechanical Engineering with a background of 5-10 years in Engineering/Project documentation. Strong written and verbal communication skills will be beneficial for effectively carrying out the responsibilities associated with this position.,

Seeking a CSV Consultant to work on a variety of validation projects including manufacturing systems, lab systems, risk assessments, etc. Some of the work may be done remotely, some at client sites and others at one of our offices. Immediate start date Job Responsibilities: Responsible for the Computer System Validation processes of the company Maintain expertise in current and emerging cGMP requirements and quality trends (e.g., 210, 211, 820, and 21 CFR Part 11) Work independently on and successfully solve problems and complete/qualify a system within given constraint of scope, time and schedule Lead system qualification efforts and be the primary client contact for coordinating work, reporting status, resolving issues, and addressing change orders as they apply Minimum Requirements: Minimum degree requirement - Bachelor's degree with at least 10+ years of experience Must be willing to travel regionally and/or nationally throughout India Candidates must have excellent verbal communication and technical writing skills Experience in generation and execution of protocols and procedures related to different areas of qualification and validation Expertise in ISPE GAMP5, ICH Q8, ICH Q9, ICH Q10, 21 CFR Part 11, Computerized System Validation, Equipment Qualification, and Validation Change Control Working knowledge of protocol development for validation of complex computer systems (e.g., multiple GAMP classes of systems); ability to develop Installation, Operational, and Performance Qualification documents Experience in execution of system validation lifecycle deliverables Experience in project execution within at least one area of systems validation (e.g., laboratory equipment, facilities utilities, manufacturing equipment) Proficient in Microsoft Word, Excel, Power Point, and Project Ability to plan and manage own work All candidates must be legally eligible to work in India

Execution of IQ, OQ and PQ for new equipment, facility & utility system, report preparation and maintenance of record. Execution of Periodic performance verification activities for equipments, facility, utilities and its report preparation. Review Initial qualification master document like URS, GxP assessment, DQ, FAT, SAT, IQ, OQ, PQ and PPV of EFU system and all executed report. Handling of departmental QMS activity through track wise software, discrepancy / deficiency activity compliance of observation, summary preparation for regulatory submission. Qualification and Periodic performance verification activity execution, compilation, review of reports [Filter integrity test (PAO), air velocity, non-viable particle count, air flow pattern as per define schedule, review of calibration certificate for measuring devices]. Ensure and updation of periodic performance verification, calibration, Bulk SIP and smoke study schedule as per available data. Review of all AHU PAO test and NVPC report form for periodic verification, Filter Replacement intimation form, Equipment/instrument inward & Deletion intimation slip & all equipments print reports during qualification. Preparation of master document for periodic performance verification of EFU system Preparation & review of SOPs through EDMS Software Execution of FAT and SAT of equipment, facility and utilities as per requirement. Equipment Periodic performance verification schedule preparation, review, updation and provide data required for monthly report preparation. QE related Instrument calibration schedule preparation (Ellab wireless system, Ellab wired system, Rotronic data loggers certificate review and updation as per available data

Title: Instrumentation and Automation Engineer Qualification: B.E in Electrical & Instrumentation Primary Responsibilities: 1. To attend /or supervise all jobs related to Instrumentation Engineering activities in site. 2. Timely execution of all calibrations of equipments/instruments as per schedule coordination with user. 3. To attend emergency breakdowns of all plant wide machines round the clock as and when required. 4. Maintain the Spare parts of all critical Instruments in site. 5. Timely execution and completion of Validation activities to be done in site. 6. Execution of all In-house Projects in instrumentation and automation in site. 7. Maintain the calibration logs, area /equipment logbooks, preventive maintenance schedule of all the activities. Audit readiness Secondary Responsibilities: 1. Preparation and Review of all documents related to engineering. Timely execution and completion of Performance verification of the equipments. Interested candidates can share your resume to [ Careers@curateqbio.com, hasumitha.chitti@curateqbio.com] with relevant subject line.