241 Osd Jobs - Page 6

Maintain the microbiology laboratory as per regulatory requirements. Planning and coordination with cross functional team for timely release of the RM,FP, Stability samples. Handling of microbiology related OOS/OOT, Deviation, Lab event. Prepare the response and closure of audit observations. Change control management for revision of SOP s, Validation protocol. Ensure the availability of resources of microbiology laboratory. Ensure the microbiologist certification program of all microbiologist. Implementation of new projects for cost saving, compliance enhancement , work simplification. Having technical knowledge of following major test MLT of OSD products and MLT validation. Disinfectant efficacy test ( Disinfectant Validation) Maintenance of microbial cultures Maintenance of Microbiological media, Growth promotion test. Autoclave validation LAF, Biosafety cabinet, Incubators, pass box validation. Objectionability assessment of identified inhouse isolates. ALCOA++ Good knowledge of various guidelines like ISO14644, HTM 2010, EU Annex 1, 4, WHO, USP chapter 60, 61, 62, 1115, 1116, 1072, 21 CFR regulations Part 210, 211 Environment monitoring program design, risk evaluation, Location selection, Alert and action limit establishment. Purified water system validation. Chemical and microbial analysis of water. 10. Audit experience for FDA, MHRA. ANVISA, TGA etc. 11. Handling of software following but not limited: SLIMS, Lonza Moda, Equisoft, Vitek 2 compact software, High air flow, ICDAS, Trackwise, EDAMS, LMS, e residue , Lab X software, TOC software 12. Hands on experience of major instruments like: Vitek 2 system, TOC analyser, Autoclave, Conductivity meter, Air sampler, Digital Microscope, LAF, Biosafety cabinet.

Role & responsibilities Candidate having experience in to OSD pharmaceuticals from QC/QA/Production/F&D/ADL

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAP Document and Reporting Compliance Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will be responsible for designing, building, and configuring applications to meet business process and application requirements. You will collaborate with teams to ensure successful project delivery and implementation. Roles & Responsibilities: Expected to be an SME 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 Lead and mentor junior professionals Conduct regular team meetings to discuss progress and challenges Stay updated on industry trends and best practices Professional & Technical Skills: Must To Have Skills: Proficiency in SAP Document and Reporting Compliance Strong understanding of SAP data structures and reporting functionalities Experience in SAP implementation projects Knowledge of SAP security and compliance standards Hands-on experience in SAP configuration and customization Additional Information: The candidate should have a minimum of 5 years of experience in SAP Document and Reporting Compliance This position is based at our Bengaluru office A 15 years full-time education is required Qualification 15 years full time education

Role & responsibilities Analytical Method development of solid oral dosage form/Semisolid/Liquid and other dosage form. Analytical Method validation of above dosage forms. CDP study: Protocol and report preparation of validation. SOP and Specs Preparation. Preferred candidate profile Minimum 4 years of experience in Analytical development laboratory MSc- Chemistry Preferred Perks and benefits Company Travel

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical products to ensure they meet established quality standards. They work in laboratories, using analytical Techniques to test raw materials, in-process samples, and finished products. Quality assurance analyst Responsible for ensuring compliance with regulatory requirements by conducting audits, inspections, and assessments Preferred candidate profile Qualification B.Pharma , B.Sc or B.Tech Biotech D.Pharma DIKSHA ( 8628944666 ) (9:30 AM to 7:30 PM ) Preferred candidate profile Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Chanigarh,Panchkula, Paonta Sahib ,BADDI ( Himachal Pradesh ) Functional : QC,QA & Production.Industry: Pharma manufacturing unit/ Food Technology The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us DIKSHA ( 8628944666 ) (9:30 AM to 7:30 PM )

Role & responsibilities 1. Production Planning and Scheduling 2. Compliance and Documentation 3. Supervision of Manufacturing Processes 4. Personnel Management and Training 5. Quality and In-Process Control 7. Process Optimization and Yield Improvement 8. Regulatory and Customer Audits Preferred candidate profile Education: B.Pharm / M.Pharm / B.Sc with strong domain knowledge in OSD manufacturing. Experience: 15+ years in pharmaceutical production, with at least 5 years in a managerial role overseeing OSD manufacturing. Regulatory Exposure: Hands-on experience in facing WHO-GMP, and other inspections. Skills: Leadership, decision-making, analytical thinking, team management, and strong knowledge of GMP and QMS.

Role & responsibilities 1. Packaging Development activities for primary, secondary & tertiary packs for Domestic, Regulated & Non-Regulated market as per marketing/Regulatory/customer requirement. 2. Monitor & control the Artwork development and approvals. 3. Getting changes made in artworks from as per marketing, Regulatory & customer requirements. 4. Preparing Master Packing Specification, Material Specification & Approved Vendor List 5. New & Periodic Vendor Audits for packing material. 6. Shade approval & shade card management. 7. Interdepartmental & vendor co-ordination & follow ups. 8. Handling packing material complaints.

Role & responsibilities Conduct in-process checks during various stages of sterile injectable manufacturing, including dispensing, compounding, filtration, filling, and sealing. Perform line clearance and area clearance before the start of manufacturing and packaging operations. Monitor aseptic practices and personnel hygiene compliance inside cleanrooms and controlled areas. Verify critical process parameters and environmental conditions during batch processing. Ensure compliance with SOPs, batch manufacturing records (BMR), and batch packaging records (BPR). Participate in visual inspection activities and oversee container-closure integrity checks. Monitor the usage and replacement of sterilized garments, materials, and equipment in aseptic areas. Raise deviations, non-conformances, and change controls as needed. Assist in investigations for OOS, OOT, or any batch-related quality issues. Provide training to operators and workers on GMP, GDP, and aseptic technique

Role Summary: OSD Production QMS is responsible for ensuring adherence to quality standards within the production process. The role involves monitoring production activities, implementing quality control measures, maintaining compliance with regulatory requirements, and driving continuous improvement initiatives. Roles And Responsibilities Quality Compliance: Implement and monitor compliance with QMS standards Industry-specific standards. Conduct periodic audits of production processes to identify deviations and enforce corrective actions. Ensure all production processes align with regulatory and company quality standards. Documentation & Reporting: Maintain and update standard operating procedures (SOPs), work instructions, and quality records. Prepare detailed reports on quality performance, including non-conformance incidents and corrective actions taken. Process Improvement: Analyze production workflows and recommend improvements to enhance efficiency and quality. Participate in root cause analysis for production issues and implement preventive measures. Key Skills and Competencies: In-depth knowledge of Quality Management Systems and standards. Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Proficiency in using quality management tools and techniques. Familiarity with relevant USFD, EU, TGA regulatory requirements and industry best practices.

Position : Section Head - Batch Release QA Functional Area: QA Reports to: QA Head Grade: G9B Department: Quality Location: Halol (OSD) POSITION SUMMARY Responsible for IPQA activity and strategy in line with Sun Pharma Compliance, Product Quality Management objectives and Regulatory requirements. Responsible for planning and arranging for internal and external departmental support of quality assurance activities as directed in approved protocols, quality systems or Procedures. Identify and implement solution for improving existing site quality assurance systems and processes Involvement in co-ordination of activities for software like SAP HANA at plant Responsible for review and Approval of Quality management/GMP records. Responsible to ensure and perform site data review of batch records for completeness of documentation, approval and rejection of materials per current good manufacturing procedures and escalation of quality incidences, Continuous process verification (CPV). Manage the batch release function at site wrt documentation, systems, approval and rejection of materials, products at the Site per current Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxPs and applicable department programs, including training, documentation, Standard Operating Procedures, and Sun Pharma Global Quality Policies, Standards and Procedures. Key responsibilities: 1. Ensure compliance to regulatory requirements on product, process, equipment and release procedures. 2. Manage Batch release activities for commercial dispatch. 3. Escalate compliance concern to concern stakeholder. 4. Review, compliance of BPR and batch release for commercial dispatch. 5. Review and approve the investigations, CAPA, and effectiveness checks with adherence to timeline. 6. Execute change control and risk assessment whenever required. 7. Ensure Quality Metrics, Quarterly BPR report as per specify timeline. 8. Ensure timely Batch release through electronic system. 9. Planning and arranging for internal and external departmental support of Quality Assurance activities as directed in approved protocols, quality systems or Procedures. 10. Follow the EHS policy and maintain the compliance to GMP requirements. 11.Co-ordination with QPs and customers of different region for batch release. 12.Management of Technical agreement with QP and Customers. 13.Responsible for oversight in warehouse and BSR. 14.Management of retain sample storage , inspection and life cycle management. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS M.sc / M. Pharm/ B. Pharm 15 years with work experience preferred. REQUIRED SUCCESS ATTRIBUTE Knowledge of GxPs, cGMP and other regulatory requirements. Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Success Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS Incumbent performs work assignments in both normal office and non-aseptic manufacturing/packaging environments. Moderate to loud noise level is common in production rooms. The incumbent must be able to comply with the gowning requirements for entry into controlled non-aseptic manufacturing areas, and wear personal protective equipment as required. This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Roles and Responsibilities Prepare dossiers for regulatory submissions (ANDA) according to US FDA guidelines. Manage CMC sections of ANDA applications, including formulations and OSD products. Coordinate with cross-functional teams for dossier preparation and submission. Ensure compliance with regulatory requirements throughout product lifecycle management. Maintain accurate records and databases related to regulatory affairs activities.

Roles and Responsibilities 1. Review of Technology data package and preparation of Gap analysis document. 2. Preparation of technology transfer protocol and report. 3. Co-ordination with FD for smooth Tech Transfer. 4. Monitoring of validation batches at production site. 5. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. 6. Review of MPCR and protocol. 7. Planning for Execution of Process design, Process qualification batch. 8. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. 9. Should be part of handling deviation, change control and failure investigations. 10. Process manufacturing parameters for Qualification batches Vs Commercial batches. 11. Preparation and reviewing of intended batch documents for regulatory submission. 12. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products.

Roles and Responsibilities Granulation: Operate and maintain granulation equipment (e.g., high shear mixers, fluid bed dryers). Perform wet and dry granulation processes, ensuring uniformity and consistency in batches. Monitor parameters like moisture content, particle size distribution, and granule flow properties. Compression: Operate tablet compression machines to produce solid dosage forms. Monitor compression parameters such as hardness, thickness, weight, and friability. Troubleshoot and adjust compression equipment to optimize production. Coating: Oversee the tablet and capsule coating processes, ensuring proper application of film coatings. Work with coating machines like pan coaters and fluid bed coaters. Monitor and control coating parameters such as spray rate, drying time, and temperature. Capsule Filling: Operate capsule filling machines to ensure accurate dosing of powder or pellets into capsules. Perform checks for capsule fill weight and ensure proper capsule sealing. Troubleshoot issues related to capsule filling, such as jammed capsules or weight discrepancies. General Responsibilities: Ensure all equipment is functioning properly and safely, adhering to preventive maintenance schedules. Maintain a clean and sterile environment in compliance with Good Manufacturing Practices (GMP). Perform in-process quality control checks to ensure that the products meet specifications. Document all activities, including batch records, machine logs, and quality checks in accordance with regulatory requirements. Collaborate with quality control and engineering teams to identify and resolve any production issues.onitor and control process parameters to ensure quality products meet specifications. Maintain accurate records of production data and perform routine maintenance tasks on equipment. Collaborate with team members to achieve daily targets and improve overall productivity. Ensure compliance with Good Manufacturing Practices (GMP) guidelines.

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.

We have been hired by a highly reputed and fast growing Pharma company to hire a "DGM - Formulation & Development' to be based at their plant located at Aurangabad . Details of the position are mentioned below: Role & responsibilities: Literature search/study and to prepare development trials strategies. Pre formulation study execution. Market/Innovator/reference product characterization. Execution and documentation of trial batches for prototype formulation development. Execution and monitoring of development stability studies. Execution of process optimization/scale-up batches. Technology transfer activities at site. Preparation/review of documents like BOM, MFR, compatibility study protocol & report, stability study protocol and report, PDR, etc as per requirements. Co-ordination with production, other relevant cross-functional departments/teams. Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc dosage forms aimed for ROW and domestic market. Should possess experience in handling various equipment like RMG, FBD/FBP, compression machine, roller compactor, coating machine, etc. Preferred candidate profile : Educational Qualification: M. Pharm Experience: 12 - 20 Years of relevant experience in a leading Pharma Company. Good Communication & Presentation skills Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak Director, Pharma Placements Inc. Mobile number: 98202 34987

Roles and Responsibilities Responsible for overall Quality System Review & Improvements Handling and control of Non-conforming products. Responsible for review & approval of key Quality System Procedures, Standard Operating Procedures & other Master Documents. GAP Analysis of the process and products. Identifying the scope of improvement based on trend analysis. Putting forward the suggestions for improvements to the Management. Participation in audits, compliance and Tracking of Audit Compliances/Status. Review & closeout of Change Controls, Deviation Complaints & CAPA. Participating in Impact assessment, investigation & approval of deviations. Review & Approval of change controls, Deviations, OOS, CAPA, Market Complaints, etc. Ensuring implementation of software based QMS in the Organization. Ensure Compliance of Software based QMS Systems. Responsible for clearance of rejected Raw & Packing Materials. Desired Candidate Profile Candidate should have good communication skills and Pharmaceutical OSD Experience required

Roles and Responsibilities Conduct quality control testing of OSD products using HPLC, GC, and other relevant instruments. Ensure compliance with GLP guidelines and maintain accurate records in LIMS system. Review batch manufacturing records (BMRs) and perform audits as required. Implement QMS procedures to ensure product quality and regulatory compliance. Collaborate with cross-functional teams to resolve quality issues.

Roles and Responsibilities Ensure compliance with cGMP guidelines during documentation, cleaning validation, equipment qualification, process validation, and OSD operations. Conduct BMR reviews, BPR reviews, change controls, deviation management, CAPA implementation, and market complaint handling. Perform QMS activities such as document issuance, master planning, batch manufacturing record review, stability analysis reports preparation. Maintain accurate records of quality systems including logbooks and protocols. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.

Roles and Responsibilities Operate and maintain granulation, compression, coating, packing machines to ensure efficient production. Ensure compliance with GMP guidelines during manufacturing processes. Monitor machine performance and troubleshoot issues to minimize downtime. Collaborate with team members to achieve production targets and quality standards. Participate in continuous improvement initiatives to enhance process efficiency.

Roles and Responsibilities Manage OSD (Oral Solid Dose) production department, ensuring compliance with cGMP guidelines. Oversee secondary packaging operations, including blister line management and cartonation activities. Supervise primary packing processes, ensuring accurate labeling and sealing of bottles/capsules. Coordinate with cross-functional teams to ensure smooth operation of the plant. Monitor quality control measures to maintain high-quality products.

Manage and maintain SCCM/MECM infrastructure, including servers, management point, distribution points, and clients. Perform health checks and routine maintenance of SCCM components. Monitor SCCM logs and troubleshoot issues related to deployments, updates, and configurations. Software & Patch Management: Deploy Windows updates, security patches, and third-party application patches using SCCM. Create and manage deployment packages for applications, drivers, and OS images. Ensure compliance with patching policies and update schedules. OS Deployment & Imaging: Configure and manage Windows OS deployment (OSD) using SCCM Task Sequences. Troubleshoot PXE boot, driver injection, and imaging related issues. Client Health & Troubleshooting: Ensure SCCM client health and remediate issues affecting deployments. Troubleshoot application installation failures, patching issues, and SCCM agent problems. Reporting & Compliance: Generate SCCM reports for software deployments, patch compliance, and inventory. Work with security teams to ensure endpoint compliance and vulnerability management. Technical Skills: Strong experience with SCCM/MECM (Current Branch ,2012, or later versions) administration. Handson experience with Software Deployment, Patch Management, and OSD. Good understanding of Windows Server (2016/2019/2022) and Active Directory. Familiarity with Intune, Azure AD, and Modern Endpoint Management.

Role & responsibilities 1. Product Strategy & Lifecycle Management: Develop and implement strategic product roadmaps for OSD products in alignment with business objectives. Conduct market research and competitive analysis to identify trends, opportunities, and threats. Manage the product lifecycle from development to commercialization, ensuring alignment with customer and regulatory requirements. 2. Business Development & Customer Engagement: Collaborate with the sales and business development teams to identify and engage potential clients. Support contract negotiations, pricing strategies, and proposals for new business opportunities. Serve as the key point of contact for clients, addressing their technical and commercial inquiries. 3. Project & Cross-functional Coordination: Work closely with R&D, manufacturing, regulatory affairs, and quality assurance teams to ensure seamless product development and commercialization. Drive project timelines and ensure deliverables are met within budget and compliance parameters. Facilitate internal and external stakeholder communication to optimize project execution. 4. Regulatory & Compliance Oversight: Ensure all OSD products comply with global regulatory requirements (FDA, EMA, MHRA, etc.). Stay updated on evolving regulatory landscapes and provide guidance to internal teams and clients. Support dossier development and regulatory submissions for product approvals. 5. Financial & Performance Metrics: Monitor product performance, profitability, and cost-effectiveness. Track KPIs and generate reports on sales, market trends, and operational efficiency. Identify opportunities for cost optimization and revenue growth. Preferred candidate profile Bachelors or Masters degree in Pharmacy, Life Sciences, Chemistry, or a related field. MBA is a plus. 6+ years of experience in product management, business development, or project management within a CDMO, pharmaceutical, or OSD manufacturing environment. Strong understanding of formulation development, tech transfer, and regulatory requirements for OSD products. Skills & Competencies: Strong analytical and strategic thinking skills. Excellent communication, negotiation, and stakeholder management abilities. Proficiency in project management tools and CRM systems. Ability to work in a fast-paced, matrix organization and manage multiple projects simultaneously. Knowledge of global pharmaceutical markets, trends, and competitive landscapes

Role & responsibilities 1. Product Strategy & Lifecycle Management: Develop and implement strategic product roadmaps for OSD products in alignment with business objectives. Conduct market research and competitive analysis to identify trends, opportunities, and threats. Manage the product lifecycle from development to commercialization, ensuring alignment with customer and regulatory requirements. 2. Business Development & Customer Engagement: Collaborate with the sales and business development teams to identify and engage potential clients. Support contract negotiations, pricing strategies, and proposals for new business opportunities. Serve as the key point of contact for clients, addressing their technical and commercial inquiries. 3. Project & Cross-functional Coordination: Work closely with R&D, manufacturing, regulatory affairs, and quality assurance teams to ensure seamless product development and commercialization. Drive project timelines and ensure deliverables are met within budget and compliance parameters. Facilitate internal and external stakeholder communication to optimize project execution. 4. Regulatory & Compliance Oversight: Ensure all OSD products comply with global regulatory requirements (FDA, EMA, MHRA, etc.). Stay updated on evolving regulatory landscapes and provide guidance to internal teams and clients. Support dossier development and regulatory submissions for product approvals. 5. Financial & Performance Metrics: Monitor product performance, profitability, and cost-effectiveness. Track KPIs and generate reports on sales, market trends, and operational efficiency. Identify opportunities for cost optimization and revenue growth. Preferred candidate profile Bachelors or Masters degree in Pharmacy, Life Sciences, Chemistry, or a related field. MBA is a plus. 6+ years of experience in product management, business development, or project management within a CDMO, pharmaceutical, or OSD manufacturing environment. Strong understanding of formulation development, tech transfer, and regulatory requirements for OSD products.

Walk In Drive For Warehouse Department In Formulation Division @ Kothur Department :- Warehouse Formulations Qualification :- BA | B Com | BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 to 8 Years Interview Date:- 05-04-2025 Interview Time:- 9.00AM TO 2.00PM Work location :- MSNF- II, Kothur Interview location :- MSN Laboratories Pvt Ltd | Formulation Unit - II, Kothur Venue Details:- MSN Laboratories Pvt Ltd| Formulation Unit -II, Kothur | Sy. No 1277&1319 -1324| Nandigama | Ranga Reddy| Telangana - 509216 Contact :- 04030449251|9200 | 8954 Note:- Candidate should bring Update Resume , Pay slips, Bank Statement, Certificates ,Aadhaar card & Pan card. About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk In Drive For Engineering Services Department In Formulation Division @ Kothur Department :- Engineering Services Formulation Qualification :- Diploma Mechanical | B Tech Mechanical Experience :- 0 to 8 Years Fresher's :- 2023 & 2024 Passed outs only Division :- Formulation Interview Date :- 05-04-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II,Kothur Venue Location :- Venue Location:-MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.