241 Osd Jobs - Page 5

Role & responsibilities Experience: 9-14 years Specialization: Oral Solid Dosage Key Responsibilities: 1. Develop and optimize formulations for OSD drug products. 2. Conduct pre-formulation studies, compatibility assessments, and stability testing. 3. Lead formulation development for OSD products, including tablets, capsules, and granules. 4. Design and optimize OSD formulations, ensuring stability and efficacy. 5. Work closely with manufacturing teams for scale-up and technology transfer of OSD formulations. 6. Ensure compliance with regulatory guidelines and GMP standards. 7. Innovate in OSD drug delivery systems and formulation strategies. 8. Develop regulatory-compliant documentation for submission. Qualifications: PhD/Masters in Pharmaceutical Sciences. Significant experience formulation development and OSD technologies. Strong understanding of regulatory requirements for OSD products. Proficiency in QbD , DoE , and process optimization. Preferred candidate profile 1. Experience of compliance with regulatory guidelines and GMP standard 2. Hands on experience of Pre -formulation studies , compatibility Assessment , stability Testing

Execute and manage technology transfer of OSD products from R&D to manufacturing. Coordinate and monitor scale-up and exhibit batches in line with regulatory requirements. Ensure USFDA and other regulatory compliance throughout product development and scale-up. Prepare and review tech transfer documents , protocols, and reports (BMRs, MFRs, PVPs, etc.). Support investigation and troubleshooting of manufacturing issues, and suggest process optimization. Collaborate with cross-functional teams: R&D, QA, RA, Manufacturing, and SCM. Participate in audits and provide technical support during regulatory inspections. Drive continuous improvement initiatives to enhance productivity, cost efficiency, and quality. Qualifications: B.Pharm / M.Pharm in Pharmaceutics or related discipline. 7-11 years of relevant experience in Tech Services Hands-on experience with OSD formulations, preferably for the US market . Proven experience in scale-up , exhibit batches , and tech transfer. Strong understanding of regulatory guidelines (USFDA) Excellent documentation, communication, and cross-functional collaboration skills.

Roles and Responsibilities Perform secondary operations such as HICART packaging. Operate blister packing machine, compression machine, coating machine, granulation machine, formulation machine (FBD), OSD machines. Ensure quality control measures are in place to maintain high-quality products. Monitor production processes to identify areas for improvement. Collaborate with team members to achieve production targets.

Vibonum Technologies Private Limted conducting a Walk-in interview for Quality Control Executives and Officers Production for its OSD Plant at Mysore. Quality Control Executive Total Vacancies - 20, Education: B. Pharm / M. Pharm / M.Sc Exp: 6-8 Years Quality Control Officer Total Vacancies - 20, Education: B. Pharm / M. Pharm / M.Sc Exp: 2-5 Years Work Location: Nanjangud Mysore Walking Address: Sai Vishram Business Hotel, Hebbagodi, 144-C/1, Kirloskar Road, opp. MTR, Bommasandra Industrial Area, Bommasandra, Bengaluru, Karnataka 560099 Google Map: https://maps.app.goo.gl/Pkh8ASL1JFpJv2An8

Vibonum Technologies Private Limted conducting a Walk-in interview for Production Supervisors and Production Officer for its OSD Plant at Mysore. Production Supervisor: Total Vacancies - 40, Education: B. Pharm / M. Pharm Exp: 5 Years and above Production Officer Total Vacancies - 40, Education: Diploma / ITI Exp: 5 Years and above Work Location: Nanjangud Mysore Walking Address: Sai Vishram Business Hotel, Hebbagodi, 144-C/1, Kirloskar Road, opp. MTR, Bommasandra Industrial Area, Bommasandra, Bengaluru, Karnataka 560099 Google Map: https://maps.app.goo.gl/Pkh8ASL1JFpJv2An8

Designing the developmental strategies for assigned products Perform feasibility assessment of new projects. Collation of developmental data for justifying the product requirements Assigning the daily activities to the team to meet the timelines of the project Co-ordinate with the analytical development to ensure the availability of development data Co-ordinate with sourcing department for the timely availability of materials for progress of the development activities. Co-ordinate with licensing department for the availability of licenses for submission batches. Co-ordinate with technology transfer/manufacturing department for smooth transfer of new products from Research and development to commercialization. Responsible for addressing regulatory deficiencies in co-ordination with cross functional teams. Preparation, approval & implementation of SOPs and relevant training activities & records. Calibration and qualification of equipment and instruments of Formulation Development Department. Ensure the compliance to the laid down systems and procedures by the team members. Ensure that the team members follow Good Documentation Practices, Quality Management systems such as Change control, deviations for continuous compliance. Responsible for designing experimental design (DoE) – composition and process optimization, statistical analysis, defining design space, statistical data interpretation and report preparation. Responsible for preparation of PDP and PDR.

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.

Alembic Pharmaceuticals Ltd. is looking for a potential candidate for the position of Research Associate in our MS&T (Technology Transfer) department based at sites nearby Vadodara . Position Criteria : B.Pharm or M.Pharm (Pharmaceutics) Minimum 1 to 5 years of relevant experience. Willingness to work at site in shifts Job Description : Execution/monitoring of Feasibility, scaleup, Validation and Verification batches. Troubleshooting of problems faced during manufacturing of post-approval change batches. To monitor all critical variables using statistical analysis. Initiation /preparation of MRS, sample request, and GMP document as per SOP. Review and Preparation of Technology transfer batch documents like BMR, MFR, Scale-up batch protocol, Scale-up batch report, Additional testing protocol (ATP), Pre-Approval Investigation Annexure and Hold time report. Assist in the Challenge study, GOP study and Critical process parameter at time of execution on shop floor. Handle Software like SAP, CONDOR, MONITOR and MES. Interested candidates can share their cv to " msnt@alembic.co.in " with a position title "RA-Tech Transfer)

We have been retained by a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development to hire a "Junior GMP Consultant - QC & QA" to be based at their HO located at Navi Mumbai. Details of the position are mentioned below: Company: Our Client is a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development. They have their head office in Mumbai and subsidiaries in Europe, Singapore, Australia and Malaysia. They have been providing high quality & credible consulting services to the Pharmaceutical Industry in India and internationally. They have a young and committed team of GMP and Regulatory Experts. Role & responsibilities: Adequate experience and well versed with Quality Control and Quality Assurance systems and procedures in accordance to regulatory standards. Hands on experience in handling HPLC, GC, UV, FTIR, etc., worked on LIMS, audit trail, CSV , familiarity with GMP, GLP, EUGMP and ICH guidelines, Should have exposure working in formulations like oral solids dosage form (OSD), injectables, etc. Experience: Min 5-10 years experience in quality control & Quality Assurance in pharmaceutical industry. Knowledge & Skills Candidate should have exposure working in QC/QA laboratory in Regulated companies. Well versed with Quality Management systems/procedures Thorough knowledge of testing Raw materials, finished product, Packing materials and handling of key instrumentation like HPLC (auto sampler), GC, dissolution testing. Well versed with QC systems & procedures, audit trail review of HPLC, GC and have knowledge of computer system validation related to QC instruments. Familiarity with GMP, GLP, EUGMP and ICH guidelines. Familiar with stability management and calibration Well versed in carrying out Analytical Method validation/verification, Analytical tech transfers. Fluency in English and good communication written and verbal. Job responsibility: 1)To assist project lead in reviewing the QC systems, documentation and practices for client. 2) Participate in Supplier audits at various sites 3) Maintaining GMP data base and preparation of SOPs 4) Ready to do extensive travelling to visit Client sites and supplier audits (domestic & international) Preferred candidate: Candidates based only in Mumbai/Navi Mumbai will be preferred. 6. Qualifications: Education: A masters degree in Pharmaceutical Sciences or a master's degree in Analytical Chemistry Skills and Competencies: Strong analytical and problem-solving skills. Attention to detail and accuracy in testing and documentation. Proficient in the use of laboratory equipment and software. 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: 98202 34987 / 81307 24980

We are hiring for the following 2 positions: Senior Executive- Quality Control RM Section Head- 5-8 Years of Experience Executive- Quality Control- Analytical Method Validation- 4-6 Years of Experience 1. Senior Executive- Quality Control- RM (Raw Material) Section Head Raw Material Testing and Release: Supervise and ensure the testing of raw materials (active pharmaceutical ingredients, excipients, packaging materials) according to approved specifications. Lead the RM team in the timely testing and release of raw materials for production use, ensuring no delays in manufacturing. Ensure that the testing of raw materials is compliant with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulatory standards. Supervision and Team Management: Lead, guide, and mentor a team of QC analysts in the RM section, ensuring effective training and development. Allocate tasks and manage workload distribution within the team to ensure smooth and efficient operations. Conduct regular performance appraisals, set objectives, and ensure team productivity and morale. Raw Material Specifications and Documentation: Review and ensure the accuracy and completeness of raw material specifications, test protocols, and related documents. Approve the testing methods and ensure compliance with the established standard operating procedures (SOPs). Ensure the proper maintenance of records related to raw materials, including stability studies, inventory control, and release certificates. Compliance and Regulatory Adherence: Ensure all raw materials and testing activities comply with the Indian Pharmacopeia (IP), USP, BP, and other regulatory standards. Ensure that all QC raw material processes are aligned with FDA, EMA, and other regulatory guidelines as applicable. Assist in audits (internal and external), and provide necessary data and reports during regulatory inspections. Equipment and Instrument Management: Oversee the calibration, maintenance, and qualification of equipment used in the RM section, ensuring accurate and reliable results. Ensure that the laboratory instruments and equipment are well-maintained and functioning optimally. Quality Control & Troubleshooting: Address any deviations, out-of-specification (OOS) results, or out-of-trend (OOT) findings related to raw material testing. Investigate and resolve any quality control issues, and recommend corrective and preventive actions (CAPAs). Lead root cause analysis and support the investigation of quality incidents related to raw materials. Vendor Management & Raw Material Supplier Interaction: Liaise with suppliers and vendors to ensure the timely and quality supply of raw materials. Participate in the selection and qualification of raw material suppliers and ensure they meet quality standards. Continuous Improvement and Efficiency: Identify opportunities for process optimization and recommend improvements to enhance operational efficiency. Ensure that the QC RM section continuously adheres to cost-effective practices, reducing wastage and improving turnaround time. Training and Knowledge Sharing: Train QC team members on analytical techniques, equipment usage, and quality control standards for raw material testing. Keep the team updated on industry trends, new regulatory guidelines, and best practices. Executive-Quality Control- Analytical Method Validation (AMV) Analytical Method Validation (AMV) : Conduct validation of analytical methods as per ICH, FDA, and other regulatory guidelines. Perform method development, optimization, and validation for raw materials, in-process materials, and finished products. Ensure adherence to validation protocols and documentation. Testing & Documentation : Oversee the execution of analytical testing for stability, release, and in-process samples. Review and verify analytical data, ensuring accuracy and completeness. Prepare and review validation reports, SOPs, and other related documentation. Compliance & Quality Assurance : Ensure compliance with GMP, GLP, ISO, and other relevant standards in laboratory activities. Support the QC team in audits (internal and external) and address any non-conformities. Ensure proper handling, storage, and disposal of chemicals, reagents, and samples in compliance with safety protocols. Equipment Maintenance : Coordinate with the maintenance team for the calibration and qualification of laboratory instruments. Perform routine checks and calibration of instruments used in testing and validation. Continuous Improvement : Actively participate in continuous improvement initiatives and training programs. Suggest and implement improvements in analytical methods and processes to enhance efficiency. Cross-Department Collaboration : Liaise with R&D, production, and regulatory teams to resolve technical issues. Assist in troubleshooting analytical issues in collaboration with the technical team

Project Role : Technology Architect Project Role Description : Review and integrate all application requirements, including functional, security, integration, performance, quality and operations requirements. Review and integrate the technical architecture requirements. Provide input into final decisions regarding hardware, network products, system software and security. Must have skills : Microsoft Intune Good to have skills : Microsoft Endpoint Configuration Manager Minimum 7.5 year(s) of experience is required Educational Qualification : BE BSc or equivalent Summary :As an Intune Architect, you will be responsible for the design, build, configure MECM infrastructure, application deployment, patch management process, OSD. Design and build Windows 10/11 SOE image, Intune configurations for Autopilot deployment, Configuration policies, MDM, Endpoint Security, Proactive Remediations, Reporting & Compliance Roles & Responsibilities:a)Ability to build new greenfield infrastructures for MECM.b)Able to build new solutions for modern device management.c)Design and plan Windows Servicing approach.d)Day to day administration of MECM environment to include engineering new solutions as needed.e)Providing technical guidance to MECM team and customer.f)Provide Tier 3 support for MECM Intune.g)Creating and updating technical documentation as required.h)Design and build Intune configurations for Windows 10 Autopilot, Configuration policies, endpoint security.i)Experience with PowerShell and OSD (Operating System Deployments)j)Configuring WDS, configuring PXE, configuring the VM build environment, and integration with MDT.k)Experience in performing large scale upgrade from windows to windows 11.l)Experience is managing deployment of device drivers. m)Experience in servicing MECM current branch infrastructures. Professional & Technical Skills:a)Should have strong experience on MECM & Intuneb)Ability to design, build and configure MECM environment.c)Design and build Windows 10 image, provide support in image rollout.d)Should be able to design policies in Intune for Windows 10/11e)Should have strong hand on Autopilot enrolments and associated configurations and rollout. Additional Information: The candidate should have a minimum of 8+ years of experience in Microsoft Endpoint Configuration Manager & Intune. The ideal candidate will possess a strong educational background in computer science or a related field, along with a proven track record of delivering impactful solutions Qualifications BE BSc or equivalent

1. Responsible for overall engineering functions of OSD & Injectable plant. 2. Responsible for O&M of utility, HVAC, Water system & process maintenance. 3. Responsible for PM/Calibration/Facility maintenance and department safety function. 4. Responsible for regulatory / statutory audit compliance at site. 5. Responsible fo preparation of maintenance reports, budget & expense control. Work Experience 18 to 22 years Education B.Tech in Mechanical Engineering Competencies

Join our EUX Technology teams and collaborate with other technology teams to ensure Infor s workstations are up-to-date using our BigFix management and Jamf for MacOS. Youll be part of our global Software Deployment team, working closely with three consistent team members in the US and Poland, with opportunities for collaboration across various IT and non-IT teams where English is the primary language. You will also be part of the MacOS Apple team with members in the US, EMEA and APAC. Enjoy a flexible workday with the ability to plan your tasks individually, focusing on tasks such as package building, BigFix system administration, Jamf Pro Administration, deployments and scripting. Regular working hours apply, with occasional exceptions with a focus on the EMEA/US work hours. (as there is where the majority of the team members are located) Essential Tasks: Software Deployment, incl BigFix MacOS Apple team, incl Jamf. Software deployment, packaging. Windows OSD team: Intune admin, Autopilot, CloudPC s Contact and collaborate with different business partners. BigFix, Intune and Jamf admin Creating packages with Bigfix, scripting,. Bash and powershell scripting 3rd line support for Windows / Apple MacOS Clients MacOS Updates and features. Windows OS Features Basic Qualifications: Resourcefulness: As a IT EUX Endpoint professional, youll need to be able to search for information and apply solutions quickly and efficiently. Were looking for individuals who can think critically and creatively to find the best solutions. Technical skills: We require good knowledge of MS Technologies, as well as experience with automation and scripting tools such as Bash scripting, BigFix relevance or other scripting languages. Communication skills: good communication skills in English, both verbal and written, are essential. We value team members who can collaborate effectively and clearly communicate technical information. Remote work adaptability: Demonstrated ability to thrive in a remote work environment, exhibiting self-motivation, independence, and proactive communication skills. Able to effectively manage tasks and responsibilities in a distributed team setup. Preferred Qualifications: Continuous learner: Proven track record of actively seeking out opportunities to expand technical knowledge and skillset. Demonstrated enthusiasm for embracing new technologies and methodologies. Adaptability and flexibility: Ability to adapt to evolving priorities and requirements in a fast-paced, dynamic environment, while maintaining a positive and proactive attitude.

Greetings from Natco Pharma Limited We are conducting Walk-in interviews for the following requirements for our formulation division in Kothur. Job Requirements Department: QA (IPQA / AQA / Qualifications / Micro QA / Documentation) - 1 to 10 Years Positions: Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc / B. Pharmacy / M. Pharmacy Hands-on experience in IPQA activities for OSD / Sterile operations. Experience in Qualification activities for all Equipments, Utilities, Instruments, and Facilities. Experience in Analytical QA & Micro QA and handling OOS, OOT, incidents, Investigations, and GLP activities. Department: Microbiology (OSD / Injectables) - 3 to 12 Years Positions: Assistant Manager / Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc (Microbiology) Experience in QMS & GLP activities and Analytical Doc review Experience in Media Preparation and Method Validations of MLT & BET Experience in Vitek-2 Operation/Culture handling/Water Sampling / Analysis Experience in Environmental monitoring activities. Preferably Male candidates Department: Engineering (QMS / Process / Electrical) - 4 to 10 Years Positions: Executive / Officer / Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: Diploma / B. Tech Hands-on experience in QMS, Documents & OQ protocol execution. Experience in Process maintenance and vendor follow-up activities. Experience in OSD Process / Packing Maintenance and Qualifications. Experience in Electrical Maintenance & Electrical substation. Should have knowledge about AutoCAD Department: Warehouse (OSD / Sterile) - 0 to 6 Years Positions: Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: B. Com / B. Sc Handling of Raw / Packing Materials Knowledge of SAP & Isolator handling Experience in Dispensing & Material Management

Roles and Responsibilities Plan Production activities Weekly, Daily & Monthly/ manager the shift production on time Preparation of all production related documents, i.e. SOPs, production formats, Machine qualifications, BMR, BPR etc. Control over quality production & production norms Guide subordinates and production operators to achieve trouble free production target Guide about GMP & its compliance Improve Productivity and cost reduction using minimum manpower Process Validations & Cleaning verification of Products for Registration Review Batch Manufacturing Record and Batch Packing Record Review online records during production operation To face Internal as well as External Agency Audits Supervising packing material and ensuring on time product delivery Categories: Allopathic and Herbal/Nutraceuticals tablets/capsules Preferred candidate profile B.Pharma /Bsc Chemistry with minimum 5 years of experience Must be good at team management production planning and execution Must be comfortable traveling to Ranjangaon MIDC, Pune If Interested, please share your updated CV on email: hr@tuliplab.com