96 Iq Jobs - Page 3

We are experts in end-to-endpharma engineering and our success is built on our relationships, both with ourcolleagues and our customers. If you want to work on projects shaping thefuture of sustainable and intelligent pharma facilities, NNE is the place tobe. Work with us We are looking for a determined and dedicated Engineer for Process Automationwho can provide innovative solutions in complete life science andpharmaceutical projects. This also includes understanding the clients complexprocess facilities, with Good Automated Manufacturing Practice (GAMP) regulatedrequirements for a pharmaceutical production facility. Our department consistsof dedicated engineers, specialized in different phases of the project includingConceptual Design, Basic Design, Detailed Design, Commissioning andQualification. Employment type: NNE employee Department : Process Automation How you might spend your days As an Engineerfor Process Automation, you'll be working with a motivated, multi-functionalteam where youll be: Responsible for deliverables in a specific area of appropriate quality and time such as: Development of functional specifications / design documents. DCS Application development based on programming standards and design guidelines. Peer reviews to ensure consistency. Testing and Verification to ensure that programming or coding is meeting functionality. Commissioning and Qualification to ensure that systems and equipment meet the requirements of end-users and regulatory agencies with cross-functional collaboration. Assisting lead/Sr. colleague on different tasks based on project phase. Contributing to technical solution within/across team. We offer you a positionwhere you will interact with highly skilled engineers within Automation in anactive and exciting environment that allows you to continue growing with newways of working at NNE. You will work in a project-oriented, internationalclimate supporting our customers and colleagues across the globe. Our projectscover the full range from small revamp projects to high-volume greenfieldproduction facilities. NNE handles projects for a vast number of internationalcustomers and intends to continue expanding our business abroad. Consequently,you may expect travelling activities of shorter or longer duration. We do not expect you toknow it all, as we ourselves need to develop and be open-minded to constantlyfind the right solutions. We are ready to welcome our new colleague(s) with aprofessional onboarding program and internal courses and training that keep ourbiggest asset you developed for the long run. Who you are At NNE,we care about who you are as a person. In the end, how you work, and yourenergy is what impacts the work we do as a team. As a person, you are: Able to perform work independently with occasional guidance and oversight by seniors. Able to apply knowledge to real life situations, learn on the job and gain practical experience. Able to take initiative, prioritize, and plan the work to reach deadlines. Having a positive approach and can be persistent when facing challenges. Customer-oriented and focused with strong professional ethics. Excellent in communication skills , curious and open-minded to learn new things. The miles youve walked. To applyfor the position there are some things that are needed, and others are a bonus.We believe these qualifications are needed for you to do well in this role: Have a degree in engineering in Electronics/Instrumentation/ Electrical/Industrial Automation or similar technical field. You have at least a minimum experience of 2-8 years in a similar field Good working knowledge of 800xA system (Control Builder , Hardware/Software), other system libraries or any other DCS/PLC automation systems. Knowledge of PCDL, PCEL libraries and SFCs would be an added advantage. Good understanding of ISA S88 Batch process & good engineering practice would be an advantage. Good understanding of Process Automation System Architecture. Have developed program from Functional specifications and system hardware specifications. Knowledge of functional specifications (Control Module, EM and Phase class) for recipes would be preferable. Experience in Integration Specs, Installation packages, Test and Qualification protocols including test plans would be preferable. FAT, SAT, IQ and OQ experience would be an added advantage.

Make your TALENTcount at NNE We are experts in end-to-endpharma engineering and our success is built on our relationships, both with ourcolleagues and our customers. If you want to work on projects shaping thefuture of sustainable and intelligent pharma facilities, NNE is the place tobe. Work with us We are looking for a determined and dedicated Advanced Engineer for ProcessAutomation who can provide innovative solutions in complete life science andpharmaceutical projects. This also includes understanding the clients complexprocess facilities, with Good Automated Manufacturing Practice (GAMP) regulatedrequirements for a pharmaceutical production facility. Our department consistsof dedicated engineers, specialized in different phases of the project includingConceptual Design, Basic Design, Detailed Design, Commissioning andQualification. Experience: Minimum 5+ years Job function : Advanced Automation Engineer Employment type : NNE employee Department: Process Automation How you might spend your days As an AdvancedEngineer for Process Automation, you'll be working with a motivated, multi-functionalteam where youll be: Responsible for deliverables where output is Medium to Complex in a specific area such as: Development of functional specifications / design documents. DCS Application coding based on programming standards and design guidelines. Peer reviews to ensure consistency. Co-ordination and alignment with cross-functional teams i.e. Process/Mech. & E/I Team Testing and Verification to ensure that programming or coding is meeting functionality. Commissioning and Qualification to ensure that systems and equipment meet the requirements of end-users and regulatory agencies with multi-discipline collaboration. Assisting lead/Sr. colleague on different tasks based on project phase. Contributing to technical solution within/across team. Demonstrating Subject Matter Expertise in a specific area. Sharing lessons learnt / guiding juniors. We offer you a positionwhere you will interact with highly skilled engineers within Automation in anactive and exciting environment that allows you to continue growing with newways of working at NNE. You will work in a project-oriented, internationalclimate supporting our customers and colleagues across the globe. Our projectscover the full range from small revamp projects to high-volume greenfieldproduction facilities. NNE handles projects for a vast number of internationalcustomers and intends to continue expanding our business abroad. Consequently,you may expect travelling activities of shorter or longer duration. We do not expect you toknow it all, as we ourselves need to develop and be open-minded to constantlyfind the right solutions. We are ready to welcome our new colleague(s) with aprofessional onboarding program and internal courses and training that keep ourbiggest asset you developed for the long run. Who you are At NNE,we care about who you are as a person. In the end, how you work, and yourenergy is what impacts the work we do as a team. As a person, you are: Able to perform work independently. Able to adapt procedures, processes, tools, equipment, or techniques to accomplish the correct output of specific assigned tasks. Able to take initiative, prioritize, and plan the work to reach deadlines. Able to make operational decisions through a choice between known alternatives. Having a positive approach and can be persistent when facing challenges. Customer-oriented and focused with strong professional ethics. Excellent in communication skills and open-minded to learn new things. The miles youve walked. To applyfor the position there are some things that are needed, and others are a bonus.We believe these qualifications are needed for you to do well in this role: Have a degree in engineering in Electronics/Instrumentation/ Electrical/Industrial Automation or similar technical field. You have at least a minimum experience of 5 years in a similar field Good working knowledge of 800xA system (Control Builder , Hardware/Software), other system libraries or any other DCS automation systems. Knowledge of PCDL, PCEL libraries and SFCs would be an added advantage. Good understanding of Process Automation System Architecture, ISA S88 Batch, pharma process, good engineering practice, GDP & regulatory knowledge would be preferable. Knowledge of Design/ functional specifications (Control Module, EM and Phase class) & application development for recipes would be preferable. Experience in Integration Specs, Installation packages, Test and Qualification protocols including test plans would be preferable. FAT, SAT, IQ and OQ experience would be preferable.

Role & responsibilities Good knowledge of QMS documents, SOP preparation, Change control initiation as per GMP norms. Good knowledge and preparation of Equipment qualification documents URS, DQ, IQ, OQ and PQ. Preparation and maintain daily log book of utility equipment, water system and HVAC system. Handling of breakdown and operation of water system and HVAC system Handling breakdown of pharma process equipment and Preparation of Preventive maintenance schedule/planner. Schedule Preparation and performing HVAC validation, Instrument calibration. Knowledge and handling of utility equipment, DG, Transformer, Air compressor, Boiler and PCC and MCC panel. Good Knowledge of deviation and CAPA documents

Academic: 1. Should have minimum qualification of M.Sc preferably in chemistry. 2. Minimum 10+ years experience 3. Academic career should be good (preferably first class and above) 4. Candidate will be preferred having good communication skill and writing Job Profile: Equipment Qualification protocol / report review DQ, IQ, OQ, PQ, FAT & SAT Should have knowledge of API process equipment like reactor, centrifuge etc. Equipment URS review, Layout, P & ID review Handling of QMS documents Like Change control, Deviations, Incidences, Performing the Investigation using different investigation tools. Performing the Risk Assessment like nitrosamine Risk Assessment, Quality risk Assessment. HVAC Qualification, PP area Qualification. Handling of temperature mapping activities. Facility Qualification

1) To prepare the Standard operating procedure for Engineering Department. 2) Operation & Maintenance of Purified Water System, UF, CSRO, HSRO, EDI & Distribution loop system 3) Operation & Maintenance of HVAC/AHU system in API Industry, Pressure balancing, Filter cleaning & area validation activity at site. 4) To prepare qualification documents DQ/IQ/OQ for the equipment to be install at site. 5) To prepare preventive maintenance schedule for the newly installed equipment. 6) To comply the Engineering related points as per cGMP & GDP practices. 7) To Orient the Engineering Team towards Updated Knowledge for cGMP and Regulatory Norms. 8) To maintain discipline with co-employees & workers. 9) To initiate & implementation ideas with respect to energy conservation. 10) To allocate manpower as per work priority. 11) To ensure the critical equipment spares as availability and Co Ordinate with engineering store. 12) To maintain engineering related documents. 13) To act as training coordinator.

Able to search and gather data on the internet via Google, LinkedIn. Develop and maintain a robust database of potential clients and industry contacts. Regularly update and verify contact information for accuracy. Conduct thorough market research to identify trends, opportunities, and challenges. Prepare comprehensive market reports, including trend analysis and market forecasts. Work closely with Sales and Marketing teams to align strategies with market trends.Role & responsibilities Preferred candidate profile Bachelor's degree in any or Marketing preferred or related field. A Master's degree is a plus. Proven experience as a Market Research Analyst or similar role. Strong proficiency in market research methodologies and tools. Excellent analytical and critical thinking skills. Detail-oriented with the ability to manage and analyze large sets of data. Effective communication skills, both written and verbal. Ability to work independently and collaboratively in a fast-paced environment. Perks and benefits Competitive salary aligned with your experience and industry benchmarks. Attractive incentive structure for each plus no limit on the incentive money. Ongoing professional development initiatives, including trainings, and other opportunities. A collaborative and inclusive work culture that cherishes diversity. Clear pathways for career advancement and personal growth within the organization. Worklife Balance Culture

Designation: Quality Assurance Chemist Location :Medchal, Hyderabad Qualification: B.sc/B.pharma Experience: Min.3 relevant exp as Qa chemist Package: 4-5LPA Shifts: General shifts If interested Contact: 8247381453 Share Cv laxmi@hireiton.com Required Candidate profile • Qualification of utilities like Purified Water systems • Reviewing BMR/BPR & issuing analytical worksheets, logbooks • Must have worked in a pharmaceutical company in the past

1. To review URS, DQ of new equipment, system & utilities like HVAC, Water system, Compressed air, Nitrogen system etc. 2. To prepare, monitor and review of qualification documents i.e. FAT, SAT, IQ, OQ & PQ protocol and reports. 3. To review all types of area layouts. 4. To execute the facility qualification for release facility in routine use. 5. To review calibration certificate of instruments. 6. To review preventive maintenance report. 7. To prepare, monitor and review temperature mapping protocol and report of equipment and area. 8. To tracking of periodic qualification of equipment, area and inform to responsible person. 9. Prepare & review of Standard Operating Procedure. 10. Preparation & review of Quality risk assessments report. 11. Preparation of Product Quality Review Report. 12. Preparation & review of Trend report of Deviation, Market Complaint, Out of Specification, Out of trend, Return Goods. 13. Release of RM/PM/FP & Intermediates in SAP system. 14. Perform internal audits of different departments. 15. Knowledge about GEMBA walk / Walk through audit in respective department and ensure the compliance of identified observations. 16. Initiation, review, evaluation & closure of change controls as initiator or QA coordinator role. 17. Issuance, archival and control of all documents likes SOPs, MPCR, format and logbook. 18. Withdrawal of raw material, intermediate/ finished product, stability, hold time and equipment cleaning (swab) samples.

About The Role Design, configure, and manage NetApp storage solutions, including ONTAP, AFF, and FAS series. Implement and maintain storage replication, backup, and disaster recovery strategies using SnapMirror, SnapVault, and MetroCluster. Perform storage provisioning, troubleshooting, and performance tuning. Work with NAS (CIFS/NFS) and SAN (FC/iSCSI) technologies for enterprise environments. Support NetApp integration with cloud providers (AWS, Azure, Google Cloud). Automate storage management tasks using PowerShell, Python, or Ansible. Collaborate with IT teams to ensure high availability, security, and efficiency of storage environments. Monitor and resolve storage-related incidents and performance issues. Required Skills & Qualifications Bachelor's degree in Computer Science, Information Technology, or a related field. Experience in NetApp storage administration. Expertise in NetApp ONTAP, SnapMirror, SnapVault, MetroCluster, and Active IQ. Hands-on experience with SAN/NAS protocols (NFS, CIFS, iSCSI, FC). Knowledge of cloud-based storage solutions (AWS FSx, Azure NetApp Files, Google Cloud). Familiarity with automation tools like PowerShell, Ansible, Python. Strong troubleshooting and problem-solving skills. NetApp certifications (NCDA, NCIE, or equivalent) are a plus. About The Role - Grade Specific Netapp Storage Admin

Email Campaign Specialist Skill-Oracle Responsys,Sql,Oracle Unity,Oracle Infinity IQ,Email Campaigns,Implementation 2Years On Ppr Team Handling Exp Mand Exp-4+Years PKG Upto-13LPA Gurgaon NP-Imm-30Days Ritika-8587970773 ritikab.imaginators@gmail.com Required Candidate profile Skill- Oracle Responsys,Sql,Oracle Unity,Oracle Infinity IQ,Email Campaigns,data Integration,CDP,Implementation,PL/SQL,AB Testing

Job description Job Title: Desktop Support Engineer | Pharma Industry | Bangalore /Hyderabad Location Company: Instrumentation and Control Solutions (ICS) Website: www.ics-india.co.in Location: Bangalore/Hyderabad Experience: 2-8 years (Pharma Industry experience mandatory) Qualification: BE/B.Tech/ Any Graduation Key Responsibilities: Maintain inventory of manufacturing automated systems, including PLCs and SCADA systems. Install and maintain computer hardware and peripherals. Install and upgrade operating systems and computer software. Troubleshoot networking and connection issues. Provide recommendations for software or hardware upgrades. Assist in 21 CFR Part 11 compliance assessments during computerized system selection. Prepare and maintain IT-related SOPs for Manufacturing Automated Systems. Participate in the qualification and validation of automated systems from an IT perspective. Prepare daily reports and manage manual backups (weekly/monthly/yearly). Manage service and incident requests via the help desk dashboard. Skills Required: Strong technical knowledge. Basic understanding of computer systems and networks. Eagerness to learn new technologies and processes. Why Join Us? Work with a reputed MNC Pharmaceutical Client. Be part of a dynamic team focused on cutting-edge technology in manufacturing automation. Enjoy a collaborative and growth-oriented work environment. Application Process: Interested candidates can share their updated resumes at hr@ics-india.co.in or contact us at 9109102346 for further details. Note: This is a full-time position requiring candidates with prior experience in the pharmaceutical industry. Connect me on LinkedIn- www.linkedin.com/in/nikita-sen-2a9565114

Works with engineers to develop sampling, quality tools, and PFMEA. Leads PPAP, ensures supplier qualification via IQ, OQ, PQ. Manages supplier list compliance with strong Supplier Quality experience in medical devices.

Role & responsibilities Mandatory Technical Skills: Good Understanding of Databases SQL server/Sybase IQ (Or any SQL database). Good knowledge of working on C++ in Linux environment Good knowledge of Python scripting Good knowledge of UNIX shell scripting Preferred Technical Skills: Knowledge of GIT Proven skills to coordinate with various teams. Prior experience in of Accounting Systems/Payments systems/Banking domain Excellent Communication Skills Preferred candidate profile 2-5 Years in Sybase Perks and benefits

1) To prepare the Standard operating procedure for Engineering Department. 2) Operation & Maintenance of Purified Water System, UF, CSRO, HSRO, EDI & Distribution loop system 3) Operation & Maintenance of HVAC/AHU system in API Industry, Pressure balancing, Filter cleaning & area validation activity at site. 4) To prepare qualification documents DQ/IQ/OQ for the equipment to be install at site. 5) To prepare preventive maintenance schedule for the newly installed equipment. 6) To comply the Engineering related points as per cGMP & GDP practices. 7) To Orient the Engineering Team towards Updated Knowledge for cGMP and Regulatory Norms. 8) To maintain discipline with co-employees & workers. 9) To initiate & implementation ideas with respect to energy conservation. 10) To allocate manpower as per work priority. 11) To ensure the critical equipment spares as availability and Co Ordinate with engineering store. 12) To maintain engineering related documents. 13) To act as training coordinator.

Position Overview: We are seeking a knowledgeable and results-driven CSV Engineer to join our team, specializing in providing expert validation services to our clients. In this role, you will work closely with a diverse range of companies, ensuring the compliance, reliability, and quality of their computerized systems while adhering to industry regulations and best practices. Key Responsibilities: Validation Strategy and Planning: - Collaborate with clients to develop tailored validation strategies and plans based on their specific needs and regulatory requirements. - Assess project scope, goals, and timelines to design efficient validation approaches. Validation Execution: - Design, develop, and execute validation protocols, including IQ, OQ and PQ to verify system functionality and compliance. - Provide on-site or remote assistance during testing and data collection phases. Documentation and Reporting: - Generate comprehensive validation documentation, such as validation master plans, Risk assessment/GxP Assessment, FS, CS, FRA, test scripts, 21 CFR PART 11 Assessment and validation reports. - Create clear and organized documentation that demonstrates compliance and traceability. Change Control and Risk Management: - Collaborate with clients to assess and manage risks associated with changes to computerized systems, ensuring proper change control procedures are followed. - Advise on the impact of changes and recommend appropriate validation strategies. Regulatory Compliance: - Stay up-to-date with relevant regulations, guidelines (e.g.,21 CFR PART 11, EU Annexure 11, cGMP, GAMP5, Data Integrity etc.), and industry trends related to computer system validation. - Apply your expertise to guide clients in meeting regulatory requirements during the validation process. Client Collaboration: - Build strong working relationships with clients, acting as a trusted advisor and validation expert. - Provide guidance, recommendations, and regular updates to ensure successful validation outcomes. Training and Support: - Provide training to Perfect Utilities engineers involved in the validation process, empowering them to understand and implement validation principles. Continuous Improvement: - Offer insights and suggestions for process improvement and optimization within the validation lifecycle. Required Qualifications and Candidate Profile: Diploma, Bachelors Degree or equivalent in technical area preferred 1-5 years of hands-on experience in computer system validation of PLC based complex system preferably across different industries and systems. Knowledge of BMS, DCS, Lab Software Validation, Vision Software Validation. Being familiar with validation principles, regulatory requirements (e.g., 21 CFR PART 11, EU Annexure 11, cGMP, GAMP5, Data Integrity etc.) Proven track record of delivering successful validation projects and ensuring compliance. Excellent communication and interpersonal skills to collaborate effectively with diverse clients. Candidate should be ready for travelling across India. Benefits: As a valued member of our team, you will enjoy the opportunity to work with a range of clients, contribute to their success, and expand your professional network. We offer competitive compensation, a dynamic and supportive work environment, and the chance to make a meaningful impact in the industry by delivering exceptional validation services. If you are a skilled CSV Engineer with a passion for assisting companies in achieving compliance and reliability in their computerized systems, we invite you to join us. Help us provide top-notch validation expertise and contribute to our clients' growth and success.

CSV Overall, 10 + Yrs. of experience in SAP CSV Validation Services. Developing validation strategies and plans for SAP implementations, upgrades, and modifications to ensure compliance with regulatory requirements. Conducting System GMP impact assessment, GAMP category assessment, ERES applicability assessment, Requirement/ Functional risk assessment after establishing communication with relevant stakeholders. Conducting change assessments and impact analyses to identify mandatory validation deliverables. Collaborating with cross functional teams, including IT, Business Process, CSV and Quality Assurance to ensure alignment on validation deliverables. Creation, execution, documentation, and review of validation plan, including FDS, BDS, TDS, test plan/ scripts, IQ/OQ/PQ Protocols, Traceability Matrix, validation reports and Release notification (Go Live). Support in defect management/ discrepancy investigation if any as part of the validation deliverables. Providing guidance and support to project teams on validation best practices and compliance requirements. Submit the complete Change/Incident/Project documentation with evidences for review and approvals by the business/quality teams. Upon acquiring all approvals, shall communicate to the development/transport/Basis teams to deploy the change/incident/project in Production environment. Ensure the change/incident/project in Production environment is deployed without any deviations. Participating in validation related meetings, training sessions. Participate in Governance reviews, status reporting and handling of escalations Keeping abreast of industry trends, regulatory changes, and best practices related to CSV in SAP. Contributing to the continuous improvement of validation processes and procedures within the organization. Support during Client Visit and Regulatory inspections.

Description 1. Ensure Review and Approval of planning, execution and documentation of Change Management Activities (at Asses / Review states); along with associated lifecycle documents and test documents for Change Lifecycle by maintaining the IT Compliance standards. 2. Responsible for the review and approval of Test Scripts and executed test cases to assure compliance with good documentation practices. 3. Individual contributor for Quality, Compliance, and Good Documentation Practices 4. Experienced in authoring review of validation documentation such as URS, FRS, and SDS, Validation Plan, Issues Log, Design Review, IQ Protocol/Report, OQ Protocol/Report, Test Cases, Test executions, Trace Matrix, and Validation report, etc. 5. Working on Defect Management, CAPA and Deviation documentation, review and approval. working on testing and validation management tools like ServiceNow, HP ALM, Document Management (GDRS/ EDMS), or equivalent tools, etc. 6. Research in supporting systems (e.g., GDRS, ServiceNow, EDMS, etc.) that store the records to be reviewed 7. Sign Approve request forms for HPQC as IT Compliance approver. Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade C Level To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) No Remote work possibility No Global Role Family To be defined Local Role Name To be defined Local Skills validation Languages RequiredENGLISH Role Rarity To Be Defined

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Tealium iQ Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years fulltime education Summary :As an Application Developer with expertise in Tealium iQ, you will be responsible for designing, building, and configuring applications to meet business process and application requirements. Your typical day will involve collaborating with cross-functional teams, developing and testing code, and ensuring the quality of the application. Roles & Responsibilities: Design, build, and configure applications to meet business process and application requirements using Tealium iQ. Collaborate with cross-functional teams to identify and prioritize application requirements. Develop and test code to ensure the quality of the application. Ensure the application is scalable, maintainable, and meets performance requirements. Provide technical support and troubleshooting for the application. Professional & Technical Skills: Must To Have Skills:Expertise in Tealium iQ. Good To Have Skills:Experience with JavaScript, HTML, CSS, and other web technologies. Strong understanding of web analytics and tag management. Experience with Agile development methodologies. Experience with version control systems such as Git or SVN. Additional Information: The candidate should have a minimum of 5 years of experience in Tealium iQ. The ideal candidate will possess a strong educational background in computer science or a related field, along with a proven track record of delivering impactful solutions. This position is based at our Bengaluru office. Qualification 15 years fulltime education

Relevant 6-8 years having Electromechanical Background. Strong experience in creating and managing documentation, such as Good Documentation Practices (GDP), in regulated industries like medical devices, pharmaceuticals, and aerospace. Proficient in statistical tools such as Minitab, with experience in techniques like ANOVA, t-tests (1t, 2t), Gage R&R, DOE (Design of Experiments), Monte Carlo simulations, and understanding statistical concepts like resolution. Solid understanding of translating Design Master Records (DMR) into production processes, with knowledge of both R&D and manufacturing activities (similar to roles like an industrialization engineer at Philips). Proven ability to communicate clearly and collaborate with global stakeholders, and effectively manage multiple manufacturing activities across teams. Experience performing and guiding product validation tests (such as TMV, IQ, OQ, and PQ) directly on the shop floor. Ideally, a background in verification or validation within regulated industries.

Project Role : Tech Delivery Subject Matter Expert Project Role Description : Drive innovative practices into delivery, bring depth of expertise to a delivery engagement. Sought out as experts, enhance Accentures marketplace reputation. Bring emerging ideas to life by shaping Accenture and client strategy. Use deep technical expertise, business acumen and fluid communication skills, work directly with a client in a trusted advisor relationship to gather requirements to analyze, design and/or implement technology best practice business changes. Must have skills : Computer System Validation (CSV) Good to have skills : Life Sciences Minimum 2 year(s) of experience is required Educational Qualification : BE Summary :As a Tech Delivery Subject Matter Expert in Business Process Architecture, you will be responsible for driving innovative practices into delivery, bringing depth of expertise to a delivery engagement. Your typical day will involve using your expertise in Computer System Validation (CSV) to analyze, design and/or implement technology best practice business changes, while working directly with clients in a trusted advisor relationship to gather requirements. Roles & Responsibilities: Lead the analysis, design and/or implementation of technology best practice business changes using your expertise in Computer System Validation (CSV). Collaborate with cross-functional teams to ensure successful delivery of projects. Provide subject matter expertise to clients and internal teams on Computer System Validation (CSV) and related topics. Stay updated with the latest advancements in Life Sciences and related technologies, integrating innovative approaches for sustained competitive advantage. Professional & Technical Skills: Must To Have Skills:Expertise in Computer System Validation (CSV). Good To Have Skills:Knowledge of Life Sciences. Strong understanding of business process architecture and related technologies. Experience in collaborating with cross-functional teams. Excellent communication and interpersonal skills. Additional Information: The candidate should have a minimum of 2 years of experience in Computer System Validation (CSV). Qualification BE

Description Talent with Lifesciences domain experience with Manual testing and GxP testing skills Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade B Level To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) No Remote work possibility No Global Role Family To be defined Local Role Name To be defined Local Skills Manual tester with GXP life science Languages RequiredENGLISH Role Rarity To Be Defined

Automation Anywhere Developer Mandatory Skills and Qualifications Needed: Must have hands on RPA development Experience and well versed on both AA V11.x and AA 360 versions. To have working knowledge of at least One programming language and Coding best practices. Experienced in feasibility Study to check technical fitment of specific process steps to RPA automation. Must have hands on experience in Solution Design (SDD/TDD) involving Web/Mainframe(Terminal Emulator)/API/PDF/SAP/SF automations Awareness and Exp in Citrix/Java based/Web Service/REST API Automations Knowledge &Experience in IQ BOT/Document Automation/ WLM/Queue mgmt./multiboot Architecture/AARI Experienced in Preparing PDD, SDD, AOH, test scenarios, UAT and Perform code review. Must have knowledge on A360 Control room, bot deployment &Credential vault management. Must have Knowledge of Reusable components. Good knowledge on DB queries & DB Connectivity handling Mentor and groom junior team members/developers in overcoming technical roadblocks. Suggest mechanisms for best performance of RPA solution & knowledge of best practices and coding standards. Capable of Identifying technical exceptions and propose handling and debugging techniques. Experience on Debug Logs and Reporting features Must complete at least A360 Advanced certification (Masters certification preferred) Experience working with one or more automation tools – BP, UiPath, Power Automate, WF etc(preferred)

Purpose of the role: This position will form an integral part in achieving all quality objectives by developing & implementing the current Quality procedures and systems in line with global regulatory expectations and industry practices. Need to work closely with all CFT team in a collaborative manner to build a Quality system. Primary Responsibility: 1. Lead all personnel and processes involved in Inspection and Packaging operations occurring on all shifts. 2. Maintain knowledge of state-of-the-art Biopharmaceutical industry standards and guidelines for inspection and packaging concepts, practices, and processes. 3. Responsible for DP facility packing activities (operation and cleaning of Visual inspection board, Plunger rod insertion & Labelling machine, Cartridge Labelling machine, Blister packing machine, Automatic Cartoning Machine, Pen Assembling and labelling machine, Cold room) related to drug product. 4. Assist the installation and commissioning activities like FAT, SAT etc. of the packing lines for Vials, PFS and Cartridge facility packing. 5. Preparation and review of the URS, QRM, IQ, OQ and PQ protocols for Plunger rod insertion & Labelling machine, Cartridge Labelling machine, Blister packing machine, Automatic Cartoning Machine, weighing balances, Pen Assembling and labelling machine, Serialization etc. 6. Ensure QMS compliance in qualification, visual inspection and packing related activities. 7. Assist the validations of equipment and the process. 8. Identify and implement the visual inspection and packing procedures with compliance to current GMP requirements. 9. Implementation of Track & Trace system for the packaging. 10.Performing the FAT & SAT of packing line equipment at vendor sites or at our facility. 11. Performing/executing the IQ, OQ and PQ related to packaging lines. 12. Performing the visual inspection activities. 13. Assisting the validation activities of other equipment like cold room, pass-box and area. 14. Prepare & review of all SOP`s/protocols related to visual inspection/packing area procedures/equipment and drug product facility. 15. Identify and implement the manufacture procedures with compliance to current GMP requirements. 16. Timely initiation, investigation, impact assessment of QMS elements.

AppBank Specialist TEAM/ROLE:AppBank Operations/AppBank Specialist TEAM OVERVIEW: AppBank Operations is a 24x7, two city model unified production management team supporting the business application of the firm using cutting-edge systems and processes that form the core of our key business, sharing best practices while providing a critical mass to help drive transformation. The team also adopts various tools developed by AppBank Engineering team to automate failures using machine learning techniques, notify discrepancies in the health of production and automation of health-restoration, with a focus on continuous measurement of risk and cost. Team members have the opportunity to work at the forefront of technology innovation alongside industry leaders and make significant contributions to the field. JOB SUMMARY: Analyst/Associate in AppBank, the Technology Divisions Run-The-Bank production management organization in customer. Specialist role in the production management function for technologies and systems that support the Firms various business functions. RESPONSIBILITIES: Work actively with team members to analyze and resolve application issues Identify defects, discrepancies, and trends by ways of code debugging or log analysis Manage incidents and effectively communicate with users, application owners and senior stakeholders across all areas Improve application stability and performance by observing patterns, recurring failures and/or issues, and advise application owners on permanent fixes accordingly Adopt various tools developed by AppBank Engineering team to automate failures using machine learning techniques and notify discrepancies in the health of production and automation of health-restoration, with a focus on continuous measurement of risk and cost. Identify alerts / processes that can be automated and then work with AppBank Engineering team in automating them Challenge existing application setup, processing and suggest different ways to solve problem or improve stability Actively participate in Change management process with view to manage risk in production environment Build and improve run books for generalists to minimize operational errors and gain fungibility/efficiency Develop reports that provide trending statistics to track and manage application health and support service performance Willing to learn and troubleshoot/support proprietary technologies not available through market place. No knowledge of proprietary technologies is required pre-hire MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS: Bachelors degree (U.S. or equivalent) and Five (5) years of software development experience MUST HAVE SKILLS AND/OR LICESNSES REQUIRED TO PERFORM THE JOB: Computer Science concept of Data Structures in practical use cases Problem solving in a development or production environment, including experience observing patterns, analyzing root cause and suggesting ideas to resolve issues Good communication skills with ability to articulate the technical and functional aspects of a development/production problem to help drive solutions with App Dev teams and senior stakeholders One of the following Structured or Object Oriented programming languages:Java, C, C++, VB, .NET, ASP or Angular etc. One of the following Scripting languages:Shell script, Perl, JavaScript or Python etc. One of the following RDBMS environments:Sybase ASE/IQ, Oracle or DB2 OPTIONAL SKILLS OR QUALIFICATION ( NICE TO HAVE ) Experience in the Financial Service Industry Experience in Cluster Computing and Big Data solutions:Spark, Hadoop, HDSF, XRS using public cloud Degree in Computer Science JD Link :

Role & responsibilities: Handling Project and maintenance of formulation pharmaceutical equipment, Handling QMS related activities like handling deviation, CCF, CAPA, Risk assessment FMECA. Preparation of DQ, IQ, SOPs for equipment. Maintain inventory for equipment spares, Handling material management by SAP, Preparation of work permit and analyse the work environment for safety Preferred candidate profile: It is compulsory to have experience in Formulation Plant Maintenance , Instrumentation, OSD & QMS . Qualification required: B.E. Mechanical/EC/IC NOTE : 1.) Experience in API, Utility will not be considered. 2.) Experience apart from OSD will not be considered