545 Osd Jobs

About The Role Project Role : Technology Support Engineer Project Role Description : Resolve incidents and problems across multiple business system components and ensure operational stability. Create and implement Requests for Change (RFC) and update knowledge base articles to support effective troubleshooting. Collaborate with vendors and help service management teams with issue analysis and resolution. Must have skills : Application Packaging Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Technology Support Engineer, you will engage in a dynamic work environment where your primary focus will be on resolving incidents and problems that arise across various business system components. Your day will involve ensuring operational stability, creating and implementing Requests for Change, and updating knowledge base articles to facilitate effective troubleshooting. Collaboration with vendors and service management teams will be essential as you analyze and resolve issues, contributing to the overall efficiency and effectiveness of the technology support operations. Roles & Responsibilities:- Expected to perform independently and become an SME.- Required active participation/contribution in team discussions.- Contribute in providing solutions to work related problems.- Assist in the development and maintenance of operational documentation to enhance team knowledge.- Engage in continuous improvement initiatives to streamline processes and enhance service delivery. Professional & Technical Skills: - Must To Have Skills: Proficiency in Application Packaging.- Good To Have Skills: Experience with software deployment tools and methodologies.- Strong understanding of incident management processes and best practices.- Familiarity with change management frameworks and their application in IT operations.- Experience in troubleshooting and resolving application-related issues. Additional Information:- The candidate should have minimum 3 years of experience in Application Packaging.- This position is based at our Bengaluru office.- A 15 years full time education is required. Qualification 15 years full time education

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D, API R&D Candidates also eligible for this positions Position : Executive / Senior Executive Qualification : M.Sc, M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 20.09.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

Job Title: Packing Supervisor OSD (USFDA Approved Plant) Job Location: Dadra Job Summary The Packing Supervisor will oversee and manage the packaging operations of oral solid dosage pharmaceutical products in compliance with USFDA, cGMP, and company standards This role ensures timely execution of packing activities, adherence to quality and safety norms, and coordination with cross-functional teams to meet production targets, Key Responsibilities Supervision & Operations Oversee day-to-day packaging operations for OSD products, Ensure compliance with USFDA, cGMP, and SOPs during all packing activities, Monitor and maintain the integrity of batch records and documentation, Quality & Compliance Ensure packaging processes meet quality standards and regulatory guidelines, Coordinate with Quality Assurance (QA) for line clearance and in-process checks, Participate in internal and external audits; address observations promptly, Team Management Lead, train, and supervise packaging personnel, Conduct performance evaluations and ensure adherence to GMP practices, Equipment & Material Management Ensure proper maintenance and calibration of packing equipment (blister, bottle, strip machines), Monitor inventory of packaging materials and initiate procurement as needed, Safety & Housekeeping Implement and enforce safety guidelines in the packing area, Maintain a clean and organized work environment, Continuous Improvement Identify process improvement opportunities and implement lean practices, Support validation activities and new product introductions, Qualifications Education: B Pharm / M Pharm in relevant field, Experience: 36 years in a USFDA-approved OSD plant, with at least 12 years in a supervisory role, Skills: Strong knowledge of USFDA, cGMP, and regulatory requirements, Hands-on experience with blister, bottle, and strip packing machines, Good leadership, communication, and problem-solving skills, Key Competencies Attention to detail and documentation accuracy, Ability to work under pressure and meet deadlines, Strong coordination with QA, QC, and Production teams, Show more Show less

Job Description Position: Technical Lead - SCCM Experience: 6 to 9 years Location: Noida Education: B.E./ B.Tech./ .MCA Primary Skills: SCCM, MECM, Intune, OSD, SCCM Infra Key Responsibilities Lead and resolve escalated MECM-related incidents and service requests. Design, deploy, and manage MECM infrastructure and client configurations. Package, test, and deploy applications across enterprise environments. Manage MECM with Intune for co-management scenarios. Perform OS deployments. Collaborate with security and infrastructure teams to ensure endpoint health and compliance. Managing OS & Boot Images Required Skills & Qualifications 6+ years of hands-on experience with MECM/SCCM in enterprise environments. Strong knowledge of Windows OS deployment using Task Sequences & WDS Experience with Intune, Azure AD, and co-management. Proficiency in PowerShell scripting and automation. Familiarity with SQL queries and reporting in MECM. Excellent troubleshooting and analytical skills. Experienced with Imaging technologies like DISM & ImageX Preferred Certifications Microsoft Certified: Endpoint Administrator Associate Microsoft 365 Certified: Endpoint Administrator Associate

Role Purpose The purpose of this role is to support delivery through development and deployment of tools. Do 1. Provide tool design, development and deployment support for the project delivery a. Interact with the internal project or client to understand the project requirement from a tool perspective b. Design the solution keeping in mind the tool requirements, current tools available as well as details on licenses required etc. c. Provide budget and timeline estimates for the tool development/ deployment as required d. For any new tool development, identify sources for development (internal or 3rd party) and work with the project managers on the development of the tool keeping in mind the production rollout timelines e. Conduct commercial discussions with the 3rd party vendors for licenses or tool development f. Conduct appropriate testing to ensure error free deployment of the tool on the project g. Ensure deployment of tool on time and within the estimated budget Mandatory Skills: MS System Center Operations Manager. Experience: 5-8 Years.

Walk In Drive for Engineering Services Department In Formulation Division @ Kothur Department:- Engineering Services OSD Skills- OSD ( Electrical | Mechanical) | Sterile Mechanical | HVAC | Water System Qualification :- ITI | Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulations Work location :-MSNF-II, Kothur Interview Date- 13-09-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- Unit-II Kothur, Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8787 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.

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

Architect SCCM/Intune setups, manage full endpoint lifecycle, enforce policies, deploy apps/OS, automate patching, monitor via Power BI, troubleshoot issues, script with PowerShell, and integrate hybrid/cloud environments. Required Candidate profile Experience with SCCM & Intune; expert in infra design, Autopilot, AAD Join, Apple DEP, Win11 deployment, app packaging, and PowerShell automation for MDM, reporting, and troubleshooting.

Architect SCCM/Intune setups, manage full endpoint lifecycle, enforce policies, deploy apps/OS, automate patching, monitor via Power BI, troubleshoot issues, script with PowerShell, and integrate hybrid/cloud environments. Required Candidate profile Experience with SCCM & Intune; expert in infra design, Autopilot, AAD Join, Apple DEP, Win11 deployment, app packaging, and PowerShell automation for MDM, reporting, and troubleshooting.

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory. Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval. Verification and review of the audit trails for Standalone, Empower and LIMS. Ensure cGMP / cGLP compliance. To follow Safety, Health and Environmental procedures and practices. Review and approval of excel sheet validations. Review results acceptance for API and Excipients and Packing material. Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols. Handling of Robotic Process Automation of Chromatography Data review (RPACD) To carry any other activities assigned by upward reporting staff. Qualification Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 3 to 7 years of experience in QC or AQA department is mandatory. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Role & responsibilities: To perform line clearance, area clearance & daily IPQA activities. To review BMR/BPR/BCR, validation protocols. To perform sampling activity at manufacturing facility. To perform facility round at shop floor. Collection of control sample and Stability sample. Issuance of LMR, BMR, ECR and maintaining the record product wise. Issuance of Finished product label & maintaining the record.

Candidate having minimum 3 to 5 year experience in Granulation, Compression & Coating section in pharmaceutical industry. Interested candidate can call on this mobile no-+91-78310 31890, 9816336040 Food allowance Health insurance Annual bonus Provident fund

ensure compliance with cGMP, cGLP, SOPs & regulatory norms. Prepare/review QMS docs (SOPs, CAPA, Deviation, OOS, Complaints). Oversee production, resource planning, validations, in-process checks & documentation (BMR/BPR). Coordinate with QA/QC/

Interview for BSC Chemistry Fresher for Packing Department for Large Formulation Pharma Company No MSC Candidates Contract Base Job Call on 9727755967 / 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Packing Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Dassault Systemes ENOVIA V5 Good to have skills : Dassault Systemes 3DEXPERIENCE ENOVIA Customization Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Lead, you will engage in the development and configuration of software systems, either managing the entire process or focusing on specific stages of the product lifecycle. Your day will involve applying your extensive knowledge of various technologies, methodologies, and tools to support clients and projects effectively, ensuring that the software solutions meet the required standards and specifications. You will also collaborate with team members to drive project success and enhance overall productivity. Roles & Responsibilities:1. Capable of understanding and contributing to the technical solution from 3DEXPERIENCE design through to code level.2. Working closely with Development Project Managers and Business Analysts to produce accurate delivery estimates and manage the transition from analysis through to 3DEXPERIENCE design and delivery.3. Provide regular and effective progress updates to and work closely with Development Project Managers to ensure the management of any delivery risks or issues.4. Participate in reviews and meetings and provide updates on project progress. Professional & Technical Skills: - Must Have Skills: Proficiency in Dassault Systemes ENOVIA V5.- Good To Have Skills: Experience with Dassault Systemes 3DEXPERIENCE ENOVIA Customization ,3DX Upgrade or Migration or Integration1 Experience on 3DEXPERIENCE 2022x or above customization and configuration 2 Experience in Web services 3 Must have Skills :3D Dashboard configuration and customization, Widget Development4 Experience in 3DX configuration and customization, Java, ADK, TCL, JSP, Spinner, MQL, DMC, JPO5 Excellent verbal and written communication skills in English and comfortable discussing technical issues6 Good Team management skills and work closely with other peers. Additional Information:- The candidate should have minimum 5 years of experience in Dassault Systemes ENOVIA V5.- This position is based at our Bengaluru office.- A 15 years full time education is required. Qualification 15 years full time education

JOB DESCRIPTION Designation: Executive Job Location: Bangalore Department: EAM About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose We are seeking a skilled and proactive Electrical and Utility Executive to oversee the maintenance, operation, and optimization of electrical systems and utility services within our facility. The ideal candidate will ensure uninterrupted power supply, efficient utility management, and compliance with safety and regulatory standards This role focuses on the engineering and maintenance of formulation injectable and OSD facility systems, supporting the engineering team in optimizing performance and enhancing organizational competency while adhering to delivery, quality, and safety standards. Responsibilities include ensuring the timely resolution of equipment breakdowns, analyzing instrument failures, and reviewing of Utility system to ensure the seamless operation of Utility, HVAC and Electrical equipment s and systems. Key Responsibilities: Maintain electrical systems including HT/LT panels and UPS systems. Operation and maintenance of all utilities during shift and day -to-day operations. Monitor and manage utility services such as BMS, water supply, compressed air, HVAC, Nitrogen, Air compressor, chilled water, Hot water and steam systems during shift hours. Conduct preventive and breakdown maintenance of electrical and utility equipment. Coordinate with vendors and contractors for service and maintenance activities. Ensure compliance with statutory regulations and safety standards. Maintain documentation related to electrical inspections, energy audits, and utility consumption. Implement energy-saving initiatives and monitor energy efficiency. Respond promptly to electrical faults and utility disruptions. Support installation and commissioning of new equipment and systems. Adherence to Standard Operating procedures, Safety, cGMP, QMS & EHS Requirements. Planning and coordinating with service provider to carry out external HVAC and maintenance activity Responsible for performing the HVAC and compressed air validation, requalification activities as per the schedule. Responsible to prepare master list and planners as per the schedule. Educational Qualification: BE/B.Tech or Diploma in Electrical and Electronics engineering (E&E) Technical/functional Skills: Trouble shooting of Utility, Electrical and HVAC equipment s. Hands-on experience with BMS, EMS and HT/LT switchgear, and other industrial control systems. Knowledge of Power distribution and load management Familiarity with relevant standards like IEC, IS. Strong knowledge of electrical systems, utility operations, and safety protocols. Ability to read and interpret electrical schematics and technical manuals. Experience: 3 6 years of experience in electrical and utility maintenance in a manufacturing or industrial setup . Behavioral Skills: Strong problem-solving and analytical abilities. Excellent communication and teamwork skills. Ability to manage multiple projects and meet deadlines. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Greetings!!!! We are looking for a QA - Manger - OSD _Chennai Location Job Description: Responsible for BMR, batch release, validations, qualifications, SOPs, GMP compliance. Handle audits, QMS (Deviation, OOS, OOT, CAPA), and technology transfer. Exposure to analytical operations will be an added advantage. Strong experience in OSD / Liquid formulation QA required. Key Skills: QA, Quality Assurance, BMR, Batch Release, Validation, GMP, SOP, QMS, Audit, Deviation, OOS, OOT, CAPA, Pharma QA. Salary: As per market standards Note: Immediate joiners preferred. Interested Candidates Kindly share your updated cv to uma@bvrpc.com

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

Role & responsibilities Perform granulation process operations as per SOP and batch requirements. Handle RMG (Rapid Mixer Granulator) machine for mixing and wet granulation. Operate and monitor FBD (Fluidized Bed Dryer) machine for drying granules. Ensure cleaning and maintenance of equipment (RMG, FBD, and associated accessories) as per cGMP and safety guidelines. Record operational parameters, cleaning logs, and maintain proper documentation. Follow SOPs, GMP, and safety protocols during operations. Coordinate with production and quality teams for smooth batch execution. Preferred candidate profile Experience: 14 years in Pharma Production (Granulation). Hands-on experience in RMG & FBD operations . Knowledge of cGMP guidelines, equipment cleaning, and documentation . Ability to work in shifts and follow strict compliance requirements.

Roles and Responsibilities Operate compression machines to produce tablets in OSD manufacturing process. Ensure accurate weight control during compression operations. Monitor machine performance and troubleshoot issues as needed. Maintain cleanliness and organization of production area. Collaborate with team members to achieve production targets. Desired Candidate Profile 1-4 years of experience in pharmaceutical production, preferably in compression operations. Strong understanding of formulation, compression, and manufacturing processes. Ability to work accurately with precision instruments and equipment. Basic knowledge of tablet coating techniques would be an added advantage.

Walk In Drive Quality Assurance Department In Formulation Division @ Kothur Department :- Quality Assurance OSD Qualification :- B Sc | B Pharmacy | M Pharmacy | MSC Experience :- 2 to 8 Years Skills:- AQA | IPQA|CQA| IPQA MFG|IPQA Packing Division :- Formulation Interview Date:- 13-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those who have experience in QA OSD (IPQA,AQA,Packing,Documentation,Validations) 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.

Roles and Responsibilities Operate and maintain OSD (Oral Solid Dose) manufacturing equipment, including compression machines, granulation lines, dispensing systems, and packaging machinery. Ensure compliance with cGMP guidelines during production operations to ensure product quality and regulatory compliance. Collaborate with cross-functional teams to resolve issues related to equipment maintenance, process optimization, and productivity improvement. Conduct routine inspections of equipment and facilities to identify potential problems before they become major issues. Participate in training programs to enhance knowledge of new technologies and procedures.

Walk In Interview at Vapi. Date : 14-09-2025 (Sunday) Designation: QC Officer-Sr. Officer Job Location: Daman Qualification: M.Sc (Chemistry). / B. Pharm/ M. Pharm Experience: 02 to 07 Years (OSD) Required Candidate profile Roles and Responsibilities: -Analytical Validation -Finished Goods -Stability -Raw material -GLP -(HPLC user must)

Job Title: HVAC Executive (MNC) Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: Minimum 5 Years Salary: Up to 7 LPA 9796871050 Job Description: We are looking for an experienced HVAC Executive to join our team in the pharmaceutical industry. The ideal candidate should have hands-on experience in HVAC system validation, operation, and maintenance along with a strong understanding of Quality Management Systems (QMS). Key Responsibilities: Ensure smooth operation, preventive maintenance, and breakdown maintenance of HVAC systems. Execute and monitor validation activities for HVAC systems as per regulatory guidelines. Maintain proper documentation in compliance with cGMP, regulatory, and company requirements. Prepare and review SOPs related to HVAC operations and maintenance. Coordinate with cross-functional teams to ensure uninterrupted facility operations. Support quality audits and inspections by providing HVAC-related documents and compliance reports. Monitor and control environmental conditions (temperature, humidity, differential pressure, etc.). Implement energy efficiency and cost optimization measures in HVAC operations. Ensure adherence to QMS standards including deviation handling, CAPA, and change control. Desired Candidate Profile: B.Tech in Mechanical related engineering discipline. Minimum 5 years of experience in HVAC operations and maintenance in a pharmaceutical manufacturing environment. Strong knowledge of HVAC validation, QMS practices, and regulatory compliance. Ability to troubleshoot HVAC equipment and systems. Excellent documentation, analytical, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Facility Management & Administration Executive / Sr. Executive Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (in Pharma Industry) Salary: Up to 7 LPA (Negotiable) 9796871050 Job Description: We are looking for an experienced Facility Management & Administration Executive/Sr. Executive with strong exposure to pharmaceutical industry facility operations. The candidate will be responsible for managing housekeeping, pest control, laundry, security, canteen services, contract labour management, and ensuring compliance with QMS and cGMP requirements. Key Responsibilities: Oversee facility management services including housekeeping, pest control, laundry, security, and canteen operations. Manage and monitor contract labour workforce ensuring compliance with labour laws and company policies. Implement and monitor QMS practices in facility operations with adherence to pharma industry standards. Coordinate with internal departments to ensure seamless support for production and administrative functions. Ensure compliance with cGMP, safety standards, and regulatory requirements in all facility-related operations. Prepare and maintain records, SOPs, and documentation related to facility management. Handle vendor management, service contracts, and negotiations. Support audits and inspections by providing facility and administration compliance documents. Drive continuous improvement initiatives in facility management and cost optimization. Desired Candidate Profile: Graduate / Diploma / MBA preferred with relevant specialization. 5+ years of experience in facility management & administration in a pharmaceutical industry. Strong knowledge of QMS, cGMP, and pharma compliance requirements. Experience in managing contract labour and third-party vendors. Excellent organizational, leadership, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: QMS Production Executive Industry: Pharmaceutical (OSD Plant) Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (OSD Pharma Plant) Salary: Around 6 LPA 9796871050 Job Description: We are seeking an experienced QMS Production Executive to join our Oral Solid Dosage (OSD) pharmaceutical manufacturing plant. The ideal candidate should have in-depth knowledge of Quality Management Systems (QMS) and hands-on experience in managing production activities in compliance with cGMP and regulatory requirements. Key Responsibilities: Ensure compliance with QMS requirements in production operations. Manage and maintain production documentation including BMR, SOPs, deviations, and change controls. Monitor and review CAPA, deviations, OOS, and audit observations related to production. Coordinate with QA, QC, and regulatory teams to ensure smooth operations. Support qualification and validation activities for equipment and processes. Implement best practices to ensure adherence to GMP, safety, and regulatory guidelines. Train production staff on QMS and compliance requirements. Support internal and external audits and regulatory inspections. Desired Candidate Profile: B.Pharm / M.Pharm or equivalent qualification. 5+ years of experience in OSD pharma production with strong QMS exposure. Strong understanding of cGMP, QMS, and regulatory compliance. Good documentation, analytical, and problem-solving skills. Ability to work independently and lead a team effectively. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Production Supervisor Industry: Pharma (MNC) Location: Bari Brahmana, Jammu Qualification: M.Sc. Chemistry / B.Pharm Experience: 3 to 6 years Salary: Up to 5 LPA Contact: 9796871050 Job Responsibilities Supervise day-to-day production activities in OSD, Capsule, and Tablet manufacturing plant . Ensure adherence to cGMP, SOPs, and regulatory guidelines during production. Monitor production processes to meet daily, weekly, and monthly targets. Maintain accurate documentation and batch records as per pharma compliance. Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations. Implement continuous improvement practices to enhance productivity and reduce wastage. Ensure proper training and guidance to operators and shop floor staff. Maintain strict compliance with EHS (Environment, Health & Safety) standards. Key Skills & Competencies Strong knowledge of pharma production processes (OSD, Tablets, Capsules). Familiarity with regulatory audits (USFDA, MHRA, WHO, etc.) . Excellent leadership, team handling, and communication skills. Ability to handle deviations, change control, and CAPA. Good problem-solving and decision-making abilities. Desired Candidate Profile 36 years of relevant experience in a reputed Pharmaceutical OSD plant . Hands-on experience in tablet/capsule manufacturing processes. Strong understanding of GMP compliance and documentation practices . Candidates with exposure to multinational pharma setups will be preferred. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: OSD Packaging Supervisor Industry: Pharmaceutical Qualification: B. Pharma Location: Bari Brahmana (Jammu) Experience Required: 2 to 5 Years Salary: Up to 5 LPA (Negotiable) 9796871050 Job Description: We are seeking a skilled and detail-oriented OSD Packaging Supervisor to join our pharmaceutical team. The candidate should have experience in Oral Solid Dosage (OSD) packaging operations, ensuring compliance with GMP standards and regulatory requirements. Key Responsibilities: Supervise daily packaging activities of OSD products as per production schedules. Ensure compliance with cGMP, SOPs, and regulatory guidelines during all packaging operations. Monitor line clearance, in-process checks, and reconciliation of packaging material. Handle and train packaging staff to maintain efficiency and quality standards. Maintain documentation including batch packaging records, deviation reports, and logbooks. Coordinate with quality assurance and production teams for smooth operations. Implement safety measures and maintain housekeeping standards in packaging areas. Support regulatory audits and inspections with packaging-related documentation. Desired Candidate Profile: B. Pharma degree is mandatory. 2 to 5 years of experience in OSD packaging operations in a pharma manufacturing setup. Knowledge of blister, strip, and bottle packaging lines. Familiarity with cGMP, QMS, and documentation practices. Strong leadership, communication, and team management skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Granulation Operator Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Qualification: ITI / Diploma Experience Required: 3 to 6 Years Salary: Up to 4 LPA 9796871050 Job Description: We are looking for an experienced Granulation Operator to join our pharmaceutical manufacturing unit. The candidate will be responsible for operating and monitoring granulation equipment and processes while ensuring compliance with cGMP and safety standards. Key Responsibilities: Operate and monitor granulation machines (RMG, FBD, multi-mill, sifter, etc.). Perform granulation activities as per SOPs, BMR, and regulatory requirements. Ensure proper cleaning, calibration, and maintenance of equipment. Monitor critical process parameters (temperature, pressure, RPM, etc.). Maintain accurate documentation of production processes and equipment logs. Support in process validation and qualification activities. Adhere to safety protocols, GMP standards, and quality guidelines. Coordinate with production, maintenance, and QA teams for smooth operations. Desired Candidate Profile: ITI / Diploma in relevant discipline. 3 to 6 years of experience as a Granulation Operator in the pharmaceutical industry. Hands-on experience in handling RMG, FBD, sifter, multi-mill, and related granulation equipment. Knowledge of cGMP, documentation, and safety compliance. Team player with good communication and problem-solving skills. https://www.linkedin.com/in/satnam-singh-37b9b518/

WALK IN DRIVE R&D MUMBAI Interested candidates need to register through the QR code or link given below (works best on Google Chrome) https://macleods.in/HR/Ad.aspx?VAL=RjFndFFJSVZWY2lSQ2ZxQXBzdzczUT09 Department : PDR Experience : 4 - 9 Years Qualification : M.Pharma/ M.Sc Location : Mumbai Job Description: 4-9 years of experience in solid oral dosage & liquid orals form in formulation & development department for regulated market Thanks & Regards HR Team