241 Osd Jobs - Page 2

Amneal Pharmaceuticals is looking for Officer, Process Development to join our dynamic team and embark on a rewarding career journey Develop and optimize manufacturing processes Support trials, validation, and scale-up activities Analyze data to improve yield and efficiency Ensure compliance with regulatory standards

Walk-in interview @ Ahmedabad For Sun Pharmaceutical Industries Limited, Dadra Date: 15th Jun 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: The Fern Residency, Ahmedabad Near Subhash Bridge Corner, RTO Circle Ahmedabad Gujarat 380027. India Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Officer / Sr. Officer Manufacturing & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 2- 6 years of experience in OSD manufacturing handling Granulation, Compression, Tablet Coating, Tablet Inspection, and Bottle Packing activities in an OSD manufacturing plant, should have knowledge of cGMP. 2) Designation: Technician Manufacturing & Packing Education: ITI / Diploma/ B. Sc Department: OSD Manufacturing & Packing Experience: 4 - 8 years of work experience in pharmaceutical company, handling Granulation, Compression, Tablet Coating, Tablet Inspection and Bottle Packing activities in a regulated manufacturing plant. For all the positions, we are looking for candidates with experience in regulated plants like USFDA, MHRA, ANVISA, TGA etc. Interested candidates meeting with criteria should carry their updated resume along with photograph, Photocopy of Salary Supporting/Appointment/latest Increment letters giving salary breakups of Monthly & Annual Salary is must. Those who are unable to attend the personal interview may send their resume by e-mail to rupeshkumar.upadhyay@sunpharma.com

Role & responsibilities Formulation Research And Development (FRD): Executes and supports formulation research & product development activities of the company to meet the pre-determined goals. Develops the formula based on information collected through literature search, innovator product details, pre-formulation studies and requirements as applicable for product and process design. Studies the effect of changing levels of key excipients such as taste masking agents, film formers, disintegrants, plasticizers etc. to establish the robustness of formulation. Finalization of excipients along with specifications and the finalized formula to yield a satisfactory physical and chemical properties including alternate excipient sourcing for optimization. Prepares SOP for the relevant R&D activities and documents like PIF, PDP, PDR, MFR. Supports the documentation of Test license NOC, Test license, Product filing for DCGI and FSSAI Product license. Supporting for execution of Pre-exhibit (Feasibility/ Scale-Up/optimization/ Pilot BE/ Placebo) batches. Raw materials sourcing Performs daily calibration of analytical/weighing balances and pH meter as per requirement. Environment, Health & Safety (EHS): Key Skills and Qualifications: Knowledge of EHS Regulations and Standards: Understanding and applying relevant regulations, such as ISO 14001, ISO 45001, and OSHA regulations. Risk Assessment and Hazard Identification: Identifying potential hazards in the workplace, including chemical, physical, biological, and ergonomic risks. Safety Program Development and Implementation: Creating and implementing safety programs, policies, and procedures. Training and Education: Providing training to employees on safety procedures, emergency response, and relevant regulations. Inspection and Monitoring: Conducting regular inspections of equipment, facilities, and work processes to ensure compliance with safety regulations. Incident Investigation: Investigating incidents, accidents, and near misses to identify root causes and implement preventative measures. Record Keeping and Documentation: Maintaining accurate records of EHS-related activities, inspections, training, and investigations. Compliance with Regulations: Ensuring compliance with environmental, health, and safety regulations and standards. Reporting and Communication: Preparing reports, communicating EHS information to management and regulatory bodies. Emergency Response: Developing and implementing emergency response plans and conducting drills. Promoting a Safety Culture: Fostering a positive safety culture within the organization. Staying Updated on Best Practices: Keeping abreast of the latest EHS regulations, standards, and technologies. Mechanical Engineering: Hands on experience on maintenance of HVAC and utility systems For maintenance of equipment's like Air handling units, process equipments, chillers, water plant, boiler, ETP & STP, Compressors, lab gases and all other utilities Perform installation, maintenance, and repair of pharmaceutical machinery. Troubleshoot and resolve technical issues promptly. Conduct regular inspections and preventive maintenance. Ensure compliance with safety and industry regulations. Collaborate with production teams to optimize machinery performance. Document service activities and generate detailed technical reports. Provide training to end-users on machinery operation and maintenance. Preferred Male candidates.

Role & responsibilities Dossier extension of already developed formulations to global regulated markets of solid oral dosage forms. Formulation development, scale up and technology transfer of newly developed solid oral dosage forms & documentation thereof. Handling of equipment used for manufacturing of solid oral dosage forms at lab as well as commercial scale. Writing laboratory note books, scale reports, QbD based product development reports, submission batch reports, master formula card, process validation reports etc. Co-ordination within the team and with cross-functional teams and assist in regulatory query response as well as assist in product filing for ROW markets.

Should have minimum 2 years of experience in OSD (Compression) Mfg. Fatte Machine

Work Location: Naidupeta, Tirupati District, Andhra Pradesh Experience Required: 8-12 years (OSD Process Maintenance) Qualification: • B.E. / B.Tech. in Mechanical, Electrical, Instrumentation or allied discipline. Key Responsibilities: • Plan, schedule and execute preventive, predictive and breakdown maintenance for OSD production and packing equipment (RMG, FBD, FBP, Fette/Sejong presses, auto coaters, capsule fillers, blister / bottle lines, etc.). • Lead troubleshooting and root-cause analysis to minimise downtime and improve Overall Equipment Effectiveness (OEE). • Prepare and control spare-parts inventory, maintenance budgets and AMCs. • Drive equipment qualification, calibration, re-validation and change-control activities in alignment with QA/Validation teams. How to Apply: Send your updated CV to: Ganesh.janne@aurobindo.com or WhatsApp: 8096888868 (Subject: AM/DM Process Maintenance OSD – ”)

Key Responsibilities: SCCM Administration & Maintenance: 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. Shifts: 24*7 rotational shifts Qualifications Bachelor s degree in Computer Science, Information Technology, or a related field.

Role & responsibilities Prepare, review and submit regulatory documents for new drug applications, product registrations, amendments and renewals to the US, Brazil, EU, India and State Level authorities. Regulatory Submissions : Prepare and submit regulatory documents, including INDs (Investigational New Drug Applications) and NDAs (New Drug Applications) to regulatory authorities. Compliance and Licensing: Ensure compliance with regulatory requirements of US, Brazil, EU & India. Liaise with regulatory authorities for drug licensing, including product registrations, renewals and manufacturing licenses for local and international markets. Ensure timely submission of import licenses and NOcs (No Objection Certificates) for imported pharmaceutical products. Regulatory Strategy: Provide strategic input on regulatory requirements for new product development, lifecycle management and post-market activities, including regulatory intelligence gathering and competitive landscape analysis. Cross Functional Collaboration: Collaborate with R&D, Clinical, Quality, Manufacturing and Marketing teams to ensure alignment with regulatory strategies and compliance. Regulatory Health Authority Communication: Act as a liaison between the company and regulatory agencies to address questions or requests regarding regulatory fillings and approvals. Documentation and Reporting: Maintain accurate and up-to-date records of regulatory agencies submissions, communications with regulatory authorities and product approval status. Regulatory Training: Assist in training internal teams on regulatory requirements and best practices to ensure overall compliance across departments. Audit and Inspection Management: Coordinate with regulatory bodies in the event of audits, inspections or investigations. Preferred candidate profile Education: Bachelor's degree in Life Sciences (Pharmacy, Biology, Chemistry or related field). Advanced degrees (e.g. Master's or Ph.D.) are a plus. Experience: Minimum 05 -07 Years of experience in Regulatory Affairs, with a focus on regulatory submissions and drug licensing in the pharmaceutical industries. Knowledge: In-depth knowledge of regulatory requirements (FDA, EMA, ICH, etc.) drug development processes and regulatory submission strategies.

Job Information Job Opening ID ZR_1895_JOB Date Opened 29/04/2023 Industry Technology Job Type Work Experience 5-8 years Job Title Network and SCCM Admin City Hyderabad Province Telangana Country India Postal Code 500081 Number of Positions 2 SCCM admin with EUC, He or she should have Min 5 years in SCCM (Packaging, Distribution and Deployment) and Min 2 years in INTUNE, Followed by good experience Min 4 years in Windows OSD, Active Directory, Azure AD,O365 L2 / L3 Level Trouble shooting. We need Network Engineer with SDWAN Cloud Genix or SDWAN Prisma, He or she should have Min 5+ years in Network Engineer and Min 2+ years in SDWAN Cloud Genix or SDWAN Prisma, Followed by 3 + experience in Palo Alto, checkpoint, FortiGate, Cisco routers and switches, Cisco wireless, F5 Load Balancing, BGP, OSPF. SCCM admin with EUC, He or she should have Min 5 years in SCCM (Packaging, Distribution and Deployment) and Min 2 years in INTUNE, Followed by good experience Min 4 years in Windows OSD, Active Directory, Azure AD,O365 L2 / L3 Level Trouble shooting. We need Network Engineer with SDWAN Cloud Genix or SDWAN Prisma, He or she should have Min 5+ years in Network Engineer and Min 2+ years in SDWAN Cloud Genix or SDWAN Prisma, Followed by 3 + experience in Palo Alto, checkpoint, FortiGate, Cisco routers and switches, Cisco wireless, F5 Load Balancing, BGP, OSPF. Location: Pan India check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#2B39C2;border-color:#2B39C2;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered=""> I'm interested

Job Responsibilities: 1. To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. 2. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. 3. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. 4. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. 5. To approve the SOPs & format, batch records relating to production operations and to ensure their strict implementation. 6. Cost: Overhead recovery, and manufacturing efficiency to be maintained. 7. Cascading Sun Values and culture to the root level. 8. People Development: Develop Talent pipelines for level II, III & IV key jobs. 9. Monitoring and control of the manufacturing environment; Process validation and calibration of analytical apparatus; Designation and monitoring of storage conditions for materials and products; compliance with GMP requirements. 10. To ensure the qualification and maintenance of department, premises and equipment. To ensure that the appropriate validations are done. 12. Retention of records; Performance and evaluation of in-process controls; 13. Training, including the application and principles of QA; 14. To design and implement the policies, systems and procedures as required for the efficient management of the shop floor.

Walk In Drive For Production OSD In Formulation Division @ Bollaram Department:- Production OSD Qualification :-ITI | BA | Diploma | B Com | BSC | B Pharmacy Experience :- 2 To 8 Years Skills :- Blister Packing | CAM & HI Cartonator | Blister CAM | Cartonatory | Capsule Filling | Roll Compactor | Compression | Coating | Granulation | Documentation | Packing Executive | Manufacturing Executive Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur | MSNF-V, Rk Puram Venue Location:- Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Coating , Granulation , Compression, Capsule Filling , Blister Packing , Cam Cartontor, Hi Cartonator, Primary Packing , Secondary Packing, Documentation. 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.

Preferred candidate profile Qualification : B Pharma/M Pharma Year of Experience : 5 - 6 Yrs in shop floor management. Must have hands on experience in Granulation Section. Having exposure of Audit facing internal and external party. Interested candidates may share profile at hr.plant@zuventus.com Job Location : Sikkim

Role & responsibilities All Packing Activities Primary And Secondary Packing Line Handled in Oral Solid Dosage From Section. To maintain and improve quality of the product as per predetermined standards. To follow the good documentation practices To allocate the man power at shop floor. To perform in process checks as per defined frequency in BPR/SOP. To coordinate and work with supervisor and team members to execute the assigned task. To Co-ordination with QA and QC dept. regarding the line clearance, samples collection and release. To co-ordinate for Preventive maintenance and calibration activities to be done. Disposal of waste generated in primary packing area. Preferred candidate profile 3 - 5 yrs of experience in OSD packing. B. Pharma/M Pharma B Sc/ M Sc are not eligible. Interested candidate may share updated profile at hr.plant@zuventus.com

HIRING! We are Hiring for Quality Assurance Department with OSD Background: QUALITY ASSURANCE Open Positions: Officer/Sr. Officer - 2 to 7 years Desire Profile : 1. Hands on experience of review of batch record and COA. 2. Well-versed in schedule M and others regulatory guidelines. 3. Knowledge of export documentations. 4. Exposure of handling regulatory and customer Audits. Interested candidates may share updated resume at hr.plant@zuventus.com

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client Name: USA based Pharma Company Position: Executive - Regulatory Affairs (Formulations for USA market) Department: Regulatory Affairs Location: Ahmedabad Job Profile: Responsible for supporting the Regulatory Affairs department in its efforts to remain in compliance with the regulations of all intended market territories (USA Market). Regulatory support for assigned projects through product development and lifecycle management of products for US market. Review and approve labels in line with US regulatory requirements for assigned products. Prepare, develop, and maintain internal Regulatory informational trackers. Prepare technical documents required for submission of dossier as per country specific requirements. Respond to consumer inquiries based on approved labels and product information. Coordinate the receipt of raw material regulatory documents from vendors. Preparation of module 1 sections including labelling sections. Perform drug listing of assigned products for US market. Support publishing of ANDA submissions Support manufacturing site for commercialization and life cycle management of the approved products. Other projects and duties as assigned by Senior Management. Desired Profile: B.Sc / B.Pharm / M.Sc / M.Pharm with 2 to 5 years experience in US regulatory affairs Labelling department with growing & well established pharmaceuticals. OTC products Experience is a Plus. Must have good exposure in supporting role of ANDA filling for USA market. Exposure in Solid Oral (Tablets & Capsules) for regulated markets (USA) would be preferred. Exposure to working in US Markets is Mandatory. Ability to compile, manage and interpret data. Ability to work both independently and within a team environment. Ability to manage several tasks simultaneously. Ability to co-ordinate & manage the project with external stake holder. Effective communicator with excellent relationship building & interpersonal skills. Proficiency in Microsoft Office and Adobe Acrobat. Strong communication skills, both verbal and written. Strong organizational skills. Recruiter's Contact Details: BEST-FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India Mobile: 09722042906, 09722052906 E-Mail: post@bfrr.in Website: www.bestfitrecruitment.co.in

Preferred candidate profile Experience: 2-6 years Role : Operator/ Supervisor Granulation/ Wurster Coating - Machines: RMG/ FBP/ FBD/ Wurster Coating/ Roll Compactor Compression - Machines: Hata/ Fette/ Korsch/ Sejong/ Killian/ Cadmach Coating - Machines: Ohara/ Glatt/ ACG Smart/ Gansons/ Bectochem Bottle Packing Operator & Supervisor, Machines: CVC/ Pharmapack/ Countec/ Labelling Blister Packing Operators, Machines: BQS/ Uhlmann/ IMAPG/ Cartonator Capsule Filling/ Inspection Operators, Machines: Sensum/ TTS/ AF90T/ AF150T/ ZRO200T/ Pressfit/ Checkweigher/ Hartnett Printing/ Band Sealing Work Location: Granules India Limited Sy No. 160/A, 161/E, 162 & 174/A, Gagillapur Village, Dundigal-Gandimaisamma Mandal, Medchal-Malkhajgiri District 500 043, Telangana, India Walk-In Interview Location: The Fern Kesarval Hotel & Spa, Verna, Bus Stand, Kesarval Gardens, Edapally - Panvel Hwy, Cortalim, Goa - 403710

Preferred candidate profile Experience: 2-6 years Role : Operator/ Technician/ Officer/ Supervisor Granulation/ Wurster Coating - Machines: RMG/ FBP/ FBD/ Wurster Coating/ Roll Compactor Compression - Machines: Hata/ Fette/ Korsch/ Sejong/ Killian/ Cadmach Coating - Machines: Ohara/ Glatt/ ACG Smart/ Gansons/ Bectochem Bottle Packing Operator & Supervisor, Machines: CVC/ Pharmapack/ Countec/ Labelling Blister Packing Operators, Machines: BQS/ Uhlmann/ IMAPG/ Cartonator Capsule Filling/ Inspection Operators, Machines: Sensum/ TTS/ AF90T/ AF150T/ ZRO200T/ Pressfit/ Checkweigher/ Hartnett Printing/ Band Sealing Warehouse - RM/ PM/ FG Engineering - Process Maintenance Work Location: Granules India Limited Sy No. 160/A, 161/E, 162 & 174/A, Gagillapur Village, Dundigal-Gandimaisamma Mandal, Medchal-Malkhajgiri District 500 043, Telangana, India Walk-In Interview Location: Elite Hotels (Manjira), Nh - 44, Sy No.100, Macharam, Jadcherla, Mahabubnagar - 509301

Number of Openings 1 ECMS ID in sourcing stage 528151 Duration of Contract 5 years Total Yrs. of Experience 10+ Relevant Yrs. of experience 10+ Detailed JD (Roles and Responsibilities) Key Responsibilities: Design, deploy, and standardize medium to large-scale SCCM environments (single to multi-tier sites). Manage Inventory, Software Distribution, Patch Management, and Image Management using SCCM. Develop and maintain custom deployment scripts (VBScript, Batch, PowerShell) for automation and compliance. Create, import, and manage Applications and Packages in SCCM. Build and troubleshoot OSD Task Sequences, including: WIM creation and capture Application deployment at build time UDI splash screen design HW driver import User State Migration (USMT) Coordinate application packaging, testing, and releases. Install, configure, and troubleshoot Distribution Points and SCCM infrastructure components. Manage Client Health across environments and resolve escalations from L2 support teams. Troubleshoot SCCM logs (client/server side) to resolve deployment and configuration issues. Implement Security Patch Management and Windows Update strategies through SCCM. Plan and administer Patch Management lifecycles. Create SCCM canned reports, SSRS dashboards, and custom SQL queries for inventory and compliance tracking. Support Mobile Device Management (MDM) integration where applicable. Provide timely documentation, status updates, and end-user support as needed. Soft Skills: Strong communication and documentation skills Proactive and detail-oriented Team player with the ability to lead initiatives when required Mandatory skills Required Skills: Deep knowledge of Microsoft SCCM/MECM Strong understanding of Windows 10/11 imaging technologies and imaging engines Hands-on with: Application creation and deployment OSD imaging and task sequencing Client health management and troubleshooting SCCM logs, SQL queries, and reporting Experience with Scripting (VBS, Batch, PowerShell) Strong problem-solving skills and ability to handle escalated incidents Experience coordinating with cross-functional teams for planning and solution design Desired/ Secondary skills Experience with Intune or MDM platforms ITIL or Microsoft certification in SCCM or Endpoint Configuration Manager Experience in retail or enterprise-scale environments Domain Retail Client Name MMS-MediaMarkt Saturn Max Vendor Rate in Per Day (Currency in relevance to work location) 12,000 INR/Day Delivery Anchor for tracking the sourcing statistics, technical evaluation, interviews, and feedback etc. Saranya, Manasa Client Interview / F2F Applicable Client Interview -Yes Work Location Offshore Start date immediately WFO/WFH/Hybrid WFO Hybrid BG Check (Pre/ Hybrid/ Post onboarding) Post Onboarding Is there any working in shifts from standard Daylight (to avoid confusions post onboarding) YES/ NO CEST Working hours

Required Skills Technology | Network Monitoring Tools | Traverse Domain | IT in Banking | Customer Support Behavioral | Aptitude | Communication Technology | Network Monitoring Tools | Solarwinds Behavioral | Aptitude | Information Processing Education Qualification : Any Graduate Certification Mandatory / Desirable : Technology | IT Certifications | Microsoft Certification | Microsoft Windows Server Networking Fundamentals Details: 1. SCCM Administration - Working knowledge of SCCM administration and related dependent components like AD, DNS, BitLocker, Group Policies etc. 2. Patch Management: a. Deployment of monthly updates on every patch Tuesday following the Change process b. Provide the patching status report to the customer 3. Software Distribution: a. Deployment of application versions to keep the devices complaint b. Provide the deployment status report to the customer 4. Hardware and Software Inventory: a. Generate hardware and software inventory reports as per the customer requirements 5. Configure features Asset intelligence, DCM, Reporting 6. Manage and administer the client settings, system discoveries, collections, boundaries and bandwidth settings etc. 7. SCCM Client installation on Servers and Desktops 8. Hands on experience on fixing SCCM/Packaging related issues on End User Windows 10 devices 9. Expertise in Windows Batch Scripting 10. Windows 10 Autopilot 11. Create and Manage Windows 10 Image with customizations, LTI and ZTI 12. OS upgradation - In-place upgrade and Feature Upgrade 13. Troubleshoot OSD Task sequence errors 14. Monitor and troubleshoot the SCCM infrastructure components and client health issues 15. Monitor and Troubleshoot: a. Monitoring the daily health of SCCM infrastructure components and client issues b. Troubleshoot failed SCCM components and clients c. Troubleshoot failed Software and Patch Deployments 16. Backup and Maintenance - Knowledge on the SCCM site backup and Maintenance tasks 17. Incident and Service Request Management - Monitor the ticket queue and act up on the reported incidents on a daily basis 18. Address the tickets escalated from L1/L2 team 19. Manage and lead team of L1/L2 Technical Skills: In-depth hands-on experience on any two of SCCM, SCOM, Traverse, SolarWinds, ManageEngine, Nexthink etc.,

Role & responsibilities Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, filling, and packing for oral dosage products. 5. SOPs and Documentation Prepare, update, and maintain Standard Operating Procedures (SOPs), BMR, and BPR documents. 6. Document Maintenance Ensure proper maintenance of documents, including BMR, BPR, cleaning records, calibration logs, environmental records, and equipment usage logbooks. 7. Manpower Allocation Allocate and manage manpower for the effective utilization of resources. 8. Production and Packing Oversight Oversee and manage the overall manufacturing and packing activities in the oral department. 9. Compliance with cGMP & GDP Monitor and implement Current Good Manufacturing Practices (cGMP) and Good Distribution Practices (GDP) within the department. 10. Quality Management System: Handle the Quality Management System (QMS), including initiating, investigating, and completing change control, deviations, and incidents. 11. Equipment & Area Qualification: Monitor and review equipment and area qualification activities and ensure timely reporting. 12. Validation Activities Coordinate with QA and QC departments for product process validation and cleaning validation activities. 13. Production Target Achievement Ensure daily and monthly production output targets are achieved. 14. Cross-Department Coordination Facilitate coordination between Quality Assurance, Quality Control, Warehouse, and Engineering departments. 15. Material Availability Check Ensure availability of required raw materials (RM) and packaging materials (PM) as per the production plan and schedule. 16. Training & Development Conduct training programs on SOPs, GMP, technical procedures, and identify training needs for department personnel. 17. BMR/BPR Handover to QA Ensure completed BMR and BPR are handed over to the QA department before dispatch activities. Required Candidate profile: 1. 07-10 years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet functions, ERP

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-10 Yrs Job Location: Pashamylaram - Patancheruv Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-7 Yrs Job Location: Pashamylaram - Patancheruv-Sangareddy Dist. Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

Execute demand planning for core and event demand at BU level - SKU, Warehouse, CSO, Customer level for Power tools Spare parts. Provide final demand to supply, inventory planning consisting of standard demand, phase-in/ phase-out, new launches, promotions, cannibalization. Lead demand validation as part of the SOP process in the respective CSOs within the region. Collaboration with BU (LOP, LOG, MKX) Sales. Ensure forecast quality and deliver related KPIs. Day-to-day operational control steering of FG supply (e. g. exception management) from plant/Buyout supplier/RDC/IDC to regional/local distribution center. Monthly Demand Review Meeting (DRM) with ChiP to align on demand fulfillment exception management. Initiate actions in case of supply issues (e. g. transportation delay) in collaboration with GS/OSD ChiP/LOG. Monitor Track material availability at CDC LDCs. Maintenance of Inventory structure material master data with ROP at CDC LDCs. Support overstock management, non-moving (>180 days) collaborate with sales MKX identify measures deployed. Single point of contact for business operations, Sales and marketing for supply-related topics. Master data maintenance update (SAP-P13, PCD Add-one). Foreign trade : Co ordination with GS/OSD, GS/OSP, Freight forwarder , CHA LSP for movement, Custom clearance and delivery.

On Roll Job with Pharma company Job Location : Ahmedabad 1. Dispensing officers 01-2 year experience Production exp required 01 Granulation officers 3-6 year experience

Manage daily production of tablets, capsules, and powders in Nutra OSD facility. Ensure compliance with cGMP, FSSAI, WHO-GMP, and internal quality standards Oversee production planning, documentation (BMRs/BPRs/SOPs), and shift management Required Candidate profile B.Pharm / M.Pharm / B.Sc / M.Sc Strong OSD & nutraceutical manufacturing experience Knowledge of regulatory compliance and production equipment Team leadership and coordination skills