WALK-IN DRIVE FOR FRESHERS We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below.Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume.QUALIFICATIONMSc Chemistry : Organic / Analytical / MicrobiologyBachelor of Science : MicrobiologyBachelor in Pharmacy Time and Venue :22nd June 2024, 09:30 Hrs to 14:00 Hrs______________________________________________________INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village,Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________We would be pleased if you forward or refer any of your colleagues matching the qualifications as mentioned.Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in.Perks and benefits

Role & responsibilities We have opening in QC & Production department. Preferred candidate profile Experience: FresherM.Sc. in Biotechnology / Microbiology / BiochemistryB.Tech. in Biotechnology / BiomedicalPerks and benefits Apprentice salary: Up to 17,000 per month1 paid leave per monthFree transportation facilitySubsidized canteen food at our facilityShare Your Updated CV on - careers_pfu@intaspharma.com

We are looking for an MBA HR student to join our HR Department for a 6-month to 1-year paid training program.The role will primarily focus on talent acquisition, including:Sourcing profiles for R&D, Production, and Quality departmentsScreening CVs and scheduling interviewsSupporting salary negotiations and offer releasesAssisting with logistics coordination and system onboardingTaking on additional responsibilities as neededWe are looking for students who are keen on building a career in talent acquisition.

Role & responsibilities Reverse Engineering of Formulations:Perform reverse engineering of reference-listed drugs (RLDs) and identify composition, excipients, and active ingredients.Utilize advanced analytical techniques for component identification and quantification.Analytical Method Development & Validation:Develop and validate HPLC, UPLC, GC, LC-MS, FTIR, UV, NMR, XRD, and DSC methods for comparative studies.Characterize excipients, degradation products, and impurities in formulations.Comparative Dissolution & Physicochemical Characterization:Conduct comparative dissolution profiling with RLD as per regulatory guidelines.Study particle size, polymorphism, stability, and compatibility of drug formulations.Regulatory Compliance & Documentation:Prepare analytical reports, method validation protocols, and regulatory documents for ANDA, USFDA, MHRA, EU-GMP submissions.Ensure compliance with ICH, USP, EP, JP, and WHO guidelines.Technology Transfer & Troubleshooting:Support technology transfer for scale-up and commercialization.Assist in troubleshooting analytical challenges during formulation development.Key Skills & Competencies: Expertise in HPLC /UPLC / GC / LC-MS / FTIR / NMR/ XRD/ DSC Knowledge of polymorphism, solubility, permeability, and excipient compatibility Experience in reverse engineering & impurity profiling Strong understanding of ICH Q2 (R1), USFDA, and regulatory guidelines Hands-on experience in GMP, GLP, and stability studies Preferred candidate profile M. Pharmacy / M.Sc (Analytical Chemistry / Pharmaceutical Chemistry / Organic Chemistry) Perks and benefits As Per Company Policy

Role & responsibilities Perform the method validation parameter as per guideline.Perform the analysis of method validation (test: Assay, RS) Exhibit Sample analysis and Forced degradation.Perform the Method Development, Pre AMV on Test Assay and RS, Routine and Scale up Batch analysis.Method Development Report (MDR), Analytical Method Validation Protocol, Analytical Method Validation Report Preparation, Method Transfer.

Role & responsibilities 1. To maintain and ensure the cGMP compliance.2. Preparation of MPCR, PVP, PVR, HSP & HSR based on TTD.3. Preparation of proposed commercial MPCR based on marketing requirements.4. Raw material tracking for the smooth functioning and timely execution of the products.5. QMS related activities (CRF/Deviation/Investigation/CAPA) and compliance.6. Follow up for CRF approval.7. Creation of HALB code and preparation of BOM in SAP8. Compilation of validation documents like Process validation report and Hold time study report.9. Any other job assigned time to time by superiors.Preferred candidate profile US Market experience in ANDA filing, CMC documentation, regulatory compliance, and technology transfer. Perks and benefits As per company policy

Job description:Should have knowledge of provisions of Tax deducted at source (TDS) and Tax collected at source (TCS) and reasonable knowledge of Income Tax Act, 1961Determining the monthly TDS /TCS liabilities and ensure timely payment of tax liabilitiesGather / Compile necessary data, prepare and file TDS / TCS returns Filing of Form 15CA for foreign remittancesEnsure reconciliation of TDS /TCS credit and corresponding income in Form 26AS vis--vis books of account, review the differences and take necessary steps for reconciliation. Help in working out quarterly advance tax instalment working, ensure timely payment of quarterly advance tax liability and helping in preparing computation of income of group companies/trustsProvide support in compiling /preparing necessary data for filing income tax return Provide support in compiling the necessary details for Assessment proceedings /TDS proceedings.Maintain proper records and documents for compliance and litigation.Stay updated on changes in Income tax law especially related to provisions of TDS/TCS and helping in implementing necessary changes in systemResolving queries relating to TDS/TCS of vendors/customersCoordination with cross functional teams for above role Proficiency in excel and working knowledge of SAP

The Product Development Leader (PDL) for Oral Solid Dosage (OSD) will play a pivotal role in leading the development of oral solid dosage forms (tablets, capsules, etc.) from early-stage formulation to commercialization. This position requires strong leadership in overseeing product development strategies, managing cross-functional teams, ensuring timely project execution, and ensuring compliance with regulatory requirements. The PDL will work closely with various internal departments such as formulation development, analytical services, regulatory affairs, and manufacturing. Role & Responsibilities:Formulation Development and Optimization:Lead the formulation development for OSD products, including immediate-release, sustained-release, and controlled-release formulations.Design, develop, and optimize drug formulations based on pre-formulation studies, physicochemical properties, and therapeutic needs.Troubleshoot formulation issues and implement innovative solutions to improve product quality and performance.Project Leadership and Management:Manage product development projects, ensuring adherence to timelines, budgets, and resources.Provide technical guidance and oversight to formulation development teams.Lead cross-functional teams to drive development from laboratory scale to pilot and commercial scale.Monitor and report on project progress, adjusting plans as needed to meet milestones.Regulatory Compliance:Ensure formulations and development processes comply with regulatory requirements (e.g., FDA, EMA, ICH, GMP).Prepare and review technical documentation, including IND, NDA submissions, stability studies, and other regulatory documents.Interface with regulatory bodies as required and support the preparation of regulatory filings.Technology Transfer:Oversee technology transfer activities from R&D to manufacturing, ensuring smooth transition and scale-up.Work closely with manufacturing teams to resolve technical issues and ensure consistency during scale-up.Collaboration & Cross-functional Interaction:Collaborate with analytical development teams to establish appropriate testing methods and specifications.Work closely with quality assurance and manufacturing to ensure compliance with SOPs and GMP standards.Collaborate with clinical and regulatory teams to develop and submit data for clinical trials and regulatory filings.Innovation and Process Improvement:Stay current with industry trends, emerging technologies, and best practices related to OSD formulations and NDDS.Identify opportunities for process improvements, cost reductions, and product innovation.Stability & Product Performance:Oversee stability studies and product performance evaluation to determine shelf-life, formulation stability, and product quality. Analyse and interpret data from stability studies and recommend formulation adjustments as needed.Desired Experience & Expertise: At least 1-5 years of experience in product development, with a focus on oral solid dosage (OSD) forms. Strong knowledge of formulation development techniques, including granulation, compression, coating, and packaging. Experience with advanced drug delivery systems (NDDS) is a plus. Demonstrated experience in project management, regulatory submissions, and technology transfer.Key Skills: Strong understanding of pharmaceutical formulation, pre-formulation studies, and drug delivery systems. Expertise in developing controlled release, extended release, and immediate-release formulations. In-depth knowledge of ICH, GMP, and regulatory guidelines.Qualification : M. Pharm with relevant function experience

Job Description : - Date : 12th to 13th March 2025 Department - Engineering Section - Electrical Position - Sr.Officer / Executive / Technician Education - Diploma Eng / ITI / BE Experience - 3 to 8 Skill Set - Have good exposure of electrical related work + formulation pharma exposure must require with OSD & Sterile facility.Section - Utility / Water SystemPosition - Sr.Officer Education - BE Experience - 3 to 5 Skill Set - Have good exposure in Water System & Utility Area + formulation pharma exposure must require with OSD & Sterile Facility Section - HVAC / BMS Position - Sr. Officer / Manager Education - BE Experience - 3 to 15 Skill Set - Have good exposure in HVAC BMS System + formulation pharma exposure must require with OSD & Sterile FacilityDate : 15th March 2025Department - Engineering Section - Plant Maintenance Sterile + OSD Facility Position - Technician Education - Diploma Eng / ITI Experience - 3 to 5 Skill Set - Have good exposure in Plant Maintenance OSD & Sterile Facility Section - Plant Maintenance Sterile & OSD Position - Assistant Manager / Manager Education - BE Experience - 12 to 15 Skill Set - Have good exposure in Plant Maintenance OSD & Sterile Facility

Walkin at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below.Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume.Role & responsibilities QUALITY ASSURANCEIPQA (Injectable) - (Officer / Senior Officer / Executive)Experience - 02 to 08 YearsQualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY ASSURANCE(QMS / Compliance / Documentation/ Validation & Qualification/OSD)(Officer / Senior Officer / Executive/Senior Executive)Experience - 02 to 08 YearsQualification - B. Pharmacy/ M Pharmacy / M.Sc. Engineering: Instrumentation / QMS(Senior Executive / Executive / Senior Officer) Experience - 03 to 09 YearsQualification BE / B tech with relevant functional experience in Calibration / Instrumentation / QMS activities Injectable - Manufacturing & Packing & Visual Inspection(Senior Executive / Executive / Senior Officer / Officer / Associate)Experience - 01 to 09 YearsQualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activitiesOSD Manufacturing & Packing( Executive / Senior Officer / Officer / Associate)Experience - 01 to 09 YearsQualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activitiesTime and Venue :29th June 2024, 09:30 Hrs to 15:00 Hrs______________________________________________________INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village,Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________We would be pleased if you forward or refer any of your colleagues matching the desired job roles.Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in.Perks and benefits

Systematic work according to regulatory compliance. Knowledge of Data Integrity , ALCOA Operation of Caliber LIMS Handling of OOS, OOT, Incident. Review of Analytical Reports of HPLC , UPLC Distribution of analytical Samples to analysts through the LIMS Software General Knowledge of Analytical Method ValidationTo maintain instrument cleaning and working area cleaning. To ensure all records / documents are maintained in compliance to regulatory requirements. To ensure all volumetric solution are prepared and standardized as per schedule. To maintain instruments logbooks properly as per analysis.

GMP Upstream roleKEY RESPONSIBILITIESCarries out the Cell and Gene Therapy manufacturing in compliance with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs)Executes manufacturing operations in clean room, following cGMP requirements and wearing sterile gowningPrepares equipment and raw materials for manufacturingPerforms (preparation and execution) aseptic process simulation (media fill)Executes all steps outlined in the batch recordsReads and fulfils in real time production batch records and equipment logbooksPerform and assures the cleaning state and routinary maintenance of the manufacturing equipmentImmediately reports any deviations occurred during manufacturing execution or preparation, errors in the documentation or any potential matter relevant for the correct completion of the manufacturing to the managementCarries out the work in compliance with company Safety PoliciesPrepares for production (engineering batch, full scale batch, clinical batch) and identification of batch specific requirementsReports any accidents, incidents and injuries immediately notifying any hazards, unsafe procedures, or conditions in the workplaceKeep up to date by participating in training courses and opportunitiesParticipates at writing and revision of SOPs and Manufacturing documentsParticipate to the quality investigation from production sideParticipates at Regulatory Authorities audits for aspects pertaining the roleSupports the activities for periodic qualification of clean room interacting with QA and engineeringIs involved in process-related meetingsCollaborates with Process Development team to bring manufacturing process in GMPExperience and KnowledgeExperience in clean room environmentsPrevious experience in fermentation and cell culture is mandatoryExperience in manufacturing of any or all - plasmids, viral vectors, or Biologics GMP upstream is essentialExperience of any or all tasks including performing aseptic fermentation and cell culture techniques, operation of large-scale bioreactors (50 to 500L) and related equipment.Good communication skills with the ability to liaise with internal and external stakeholders Showing initiative in executing plans and delivering objectives. Problem solving mindset.Strong team player QualificationsBSc or MSc Degree or equivalent in Life Sciences or Biological / Chemical Engineering with 3-5 years of experience in cGMP setting.

GMP Downstream roleKEY RESPONSIBILITIESCarries out the Cell and Gene Therapy manufacturing in compliance with Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs)Executes manufacturing operations in clean room, following cGMP requirements and wearing sterile gowningPrepares equipment and raw materials for manufacturingPerforms (preparation and execution) aseptic process simulation Executes all steps outlined in the batch recordsReads and fulfils in real time production batch records and equipment logbooksPerform and assures the cleaning state and routinary maintenance of the manufacturing equipmentImmediately reports any deviations occurred during manufacturing execution or preparation, errors in the documentation or any potential matter relevant for the correct completion of the manufacturing to the managementCarries out the work in compliance with company Safety PoliciesPrepares for production (engineering batch, full scale batch, clinical batch) and identification of batch specific requirementsReports any accidents, incidents and injuries immediately notifying any hazards, unsafe procedures, or conditions in the workplaceKeep up to date by participating in training courses and opportunitiesParticipates at writing and revision of SOPs and Manufacturing documentsParticipate to the quality investigation from production sideParticipates at Regulatory Authorities audits for aspects pertaining the roleSupports the activities for periodic qualification of clean room interacting with QA and engineeringIs involved in process-related meetingsCollaborates with Process Development team to bring manufacturing process in GMPExperience and KnowledgeExperience in clean room environmentsPrevious experience in downstream purification is mandatoryExperience in manufacturing of any or all - plasmids, viral vectors, or Biologics GMP upstream is essentialExperience of any or all tasks including performing filtration, chromatography and associated techniques is essentialGood communication skills with the ability to liaise with internal and external stakeholders Showing initiative in executing plans and delivering objectives. Problem solving mindset.Strong team player

Role & responsibilities - Support manufacturing process of Upstream and downstream manufacturing of Monoclonal antibodies.- Handling of AKTA chromatography system, TFF process ,different type of filtration, Bioreactors.- Involved in Media and Buffer preparation activities.- Proper documentation of batches as per SOPs and written procedures.- Ensuring compliance to cGMP in cell culture area as defined in SOP.- Responsible for general area cleanliness, sanitation and compliance to bio safety policies of cell culture.

Role & responsibilities Quality Control- RMPM

Skill Required:Aseptic operationUpstream/Downstream processing Cell culture/MicrobialKnowledge for MAbs/Fermentation/Protein purification Job Description:Proper execution and processing of microbial operations for all commercial, test and validation batches as per production schedule.Proper documentation of batches as per SOPs and written procedures.Ensuring compliance to cGMP in cell culture/microbial area as defined by SOPs of BBM.Preparation & revision of equipment and process related SOPs of cell culture/microbial area.Responsible for general area cleanliness, sanitation and compliance to bio safety policies of cell culture/microbial area.Learn media preparation activities of cell culture/microbial operations.Compilation of documents for the raw material and consumables used in cell culture/microbial process.Qualification of new equipments. Preparation of Qualification documents (URS, DQ, IQ, OQ and PQ).Data compilation and trend updation.

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

1. Ensure compliance of all applicable acts & rules and regulations related to Environment, Health and safety. 2. Developed & maintained ETP laboratory for effective operation of wastewater treatment plant. 3. Keep close observation on various waste generation pattern like wastewater, solid waste, incinerable / co-processing waste etc. and ensure that all the waste generation are within the prescribed / defined limit. 4. Ensure effective management of Hazardous & other waste management by close coordination with M/s BEIL, & other waste disposal facility. 5. Ensure effective implementation & compliance of SOPs related to EHS dept. 6. To prepare monthly / annual form-3, 4 & format related to EHS like XGN report, Hazardous waste statement, Mock drill report etc. 7. Ensure highest standard of safety compliance by timely identified & rectified unsafe condition & unsafe action by proactive approach. 8. Carry out Safety Audits, & Risk Assessment. 9. Ensure that there will no accident / incident at site. 10. Ensure effective implementation of on-Site Emergency plan by regular conducting Mock drill & fire drill. 11. Keep all the records related to EHS, updated condition to ensure compliance of all applicable Acts & rules related to Environment, Health, and safety 12. To prepare and submit Environmental Statement (Form-V) to Pollution Control Board & to ensure preparation of Environmental Audit Reports.13. Work on waste optimization generates from various industrial operations / manufacturing processes. 14. Effective operation & maintenance of Effluent Treatment Plant / Waste management plant / MEE plant / RO Plant. 15. Preparation and Review of SOPs related to EHS dept. & ensure effective implementation of same. 16. Effective implementation of on-Site Emergency plan. 17. Ensure healthy condition of firefighting equipment & system. 18. Developed EHS culture in organization through training & motivational programs. 19. Formation & Setting up Safety Committee, Conducting of committee meeting & preparation of minutes of meeting. 20. Ensure to project activities w.r.t. EHS activities & take active participation in execution work of waste management facilities projects. 21. Ensure that all the applicable GMP related, quality related and procurement related requirements are fulfil and complied on time.

Requirement for R&D chemistChemical Research & Analytical Research activities to be performedHands on experience of instrument like HPLC & GC

Chromatographic skills like SEC, IEX, HIC, RP, etc with operation of HPLC, UPLC equipments. N-Glycan analysis is preferred and higher order structure analysis experience will be advantage. Electrophoresis skills like Capillary electrophoresis (cIEF, CE-SDS NR & R, CE-LIF) etc. Work experience on analytical method development and validation for biotherapeutic products. Experience on documentation preparations like SOPs, MOA, MDR, etc. Computer literacy in Microsoft office and softwares related to critical equipments

Job Summary: The role involves executing various drug product development studies, preparing stability protocols, compiling data, conducting trend analysis, and preparing stability reports for projects. The responsibilities include supporting technology transfer, troubleshooting issues with finished products, coordinating stability studies with other departments, and handling related equipment maintenance.Key Responsibilities:Prepare draft reports for formulation development summaries and stability data. Support technology transfer and process validation batches. Troubleshoot issues related to the finished product process. Execute stability studies in coordination with other departments and prepare reports. Handle and maintain stability chambers and instruments, as requested by the supervisor. Provide training to trainees. Review stability data generated using various techniques, including chromatography. Prepare responses to queries from different regulatory markets. Plan and execute various drug product development studies, such as Filter Adsorption Study, Tubing/Closure Compatibility, Hold Time Study, Shear Stress, and Freeze/Thaw Study. Respond to QA observations and close reports; review and ensure SOP compliance

Function: Business Finance FP&A (Emerging Market)CA/MBA with ~ 6-10 years of experience.Brief Job roleReview of Business case and agreements for In License productsSupport and Lead BPC projectAnalyzing the business model deployed by countryDoing ROI analysis for investment Vis a Vis return from businessReview in market inventory situation and prepare liquidation plan in consultation with country financeMonitoring of working capital and Monthly cash flow forecastAssisting business leader in various report / analysis for respective territoryAny other critical Ad hoc projects Good In communication, Analytical Skill & Project Management.

Position Manager SAP ABAPLocation AhmedabadNote : This role we are looking for work from office only. DO ot have WFH or Hybrid facility.Roles & ResponsibilitiesWork as ABAP ProgrammerPreparation of Technical Specification, Unit testing, contribute to integration testing, and/or be responsible for the design and delivery of end-user training.Assure compliance with the programming and documentation standards.Review program codes and correct ABAP program errors.Maintain and update existing program codes as needed.Assure technical development estimations for assigned project.Maintaining, optimizing, and improving applications and systems. Desired Skills & ExperienceQualification B Tech / M Tech / MBA / MCAPreference - Pharma work Experience and SAP Certification in ABAP5+yr of Strong experience in ABAP design, testing and debugging work related to the implementation, enhancement, and support of SAP modules. Must have Skills:Should have strong hands-on experience in SAP ABAP Development.Strong Experience in Code Remediation and Standard SAP Remediation tools.Should have strong hands-on experience in ABAP dictionary, Reports, SAP Scripts, Smart forms, Adobe forms, Dialog programming, Interface programming, ALE/IDOCs, Enhancements, OOPs. Strong ABAP development experience in RICEFW Forms (Adobe also preferable).Knowledge on Performance tuning and interfacing technologies.Working knowledge on Object Oriented ABAP.Hands on experience on Module pool programming.Good Knowledge of ABAP debugging.Handling various inbound/outbound standard/custom IDOC types.Self-starter, works independently.Basic knowledge of SD, MM, PP, FI and QM Modules.Strong verbal and written communications skills, with an ability to express complex technical concepts in business terms and in English. EWM Technical knowledge will add the advantage

Job Title: Asst. Manager Operation Finance Greece Department : Finance Location : AhmedabadSpecific Job Responsibilities: Product Costing & ERP Standard cost release in SAP for FG/SFG to ensure compliance with the global costing policy. Perform month-end closing activity to maintain financial integrity. Variance analysis on monthly basis to identify major drivers. Providing cost estimates to the business to support future business and commercial teams across Europe. Operational Inventory valuation from SAP for all material categories i.e. RM/PM/SFG/FG/WIP. Front foot involvement in SAP various modules role out for operational site.Budgets Ensure standard costs and routing are up to date to ensure accurate costing for new financial year. Perform annual cost release for the new financial year in compliance with global costing policy. Cost center wise opex budget with detailed clarificationMIS & Financial Reporting Operational MIS reporting with detailed reason for deviation as compared to budget. Provide MIS vs financial profitability detailed reconciliation item wise. Provide reports and analysis on production outputs as part of weekly and month end reporting. Develop periodic and adequate reporting for site. Monthly FI period closure after thorough check for IC balance, provisions.These are the main functions of the role; however, employees may be required to carry out other, ad hoc duties, as may be reasonably required. There will also be an expectation of EU travel Relevant Professional / Educational Background, Skills & Experience: CA/ICWA qualified with a strong academic profile Minimum 5 years post qualification experience in a Multinational manufacturing company (preferably pharmaceutical or FMCG industry)Strong communication and interpersonal skillsStrong cultural awareness ensuring an ability to work with global colleaguesCapable of working on own initiativeTeam player demonstrating maximum flexibility as required to complete key tasksStrong administration, attention detail, technically advanced in IT and data management.Passionate dynamic manager with a strong presence with the ability to inspire staff, deliver to deadlines and manage expectations with confidence.Able to handle multiple priorities and critical decision making within tight time constraintsFlexible and thrive in fast paced, changing environment. Commercial outlook and ability to understand business priorities and challenges.

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below.Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume.Role & responsibilities Injectable - Manufacturing & Packing & Visual Inspection(Senior Executive / Executive / Senior Officer / Officer / Associate)Experience - 01 to 09 YearsQualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activitiesOSD Manufacturing ( Executive / Senior Officer / Officer / Associate)Experience - 01 to 09 YearsQualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activitiesTime and Venue :05th April 2025, 09:30 Hrs to 14:00 HrsSATURDAY______________________________________________________INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village,Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________We would be pleased if you forward or refer any of your colleagues matching the desired job roles.Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in.Perks and benefits

Exciting Career Opportunity for Fresher B.Sc. Graduates!Are you a passionate B.Sc. graduate eager to kick-start your career? We are looking for dynamic and enthusiastic individuals to join our team!Department - Quality Control LabPosition - Trainee (Staff Grade) Education - B.Sc Graduate Specializing in Chemistry & Microbiology) with Minimum 55 % are require. (Pass Out 2023-2024 / 2024-2025)Skill Set Require - - Strong analytical & problem-solving abilities- Good communication skill in English & teamwork skills- Willingness to learn & grow Time (Registration): 09.00 a.m. to 02.00 p.m.Job Location: Intas, Pharmez, AhmedabadInterview Venue: Intas Pharmaceutical Limited, Plot no. 05 to 14, Pharmez, Near Village Matoda, Sarkhej Bavla Highway 8-A, Taluka- Sanand, Dist- Ahmedabad. Why Join Us? Hands-on training & career growth opportunities Supportive work environmentNote: - Ready to work in all shift are mandatory (first / second / general & night)

Cyber Security Analyst1. Planning, implementing, managing, monitoring, and upgrading security measures for the protection of the organizations data, systems, and networks2. Ensuring that the organizations data and infrastructure are protected by enabling the appropriate security controls3.monitor and respond to common cyber threats such as 'phishing' emails, 'pharming' activity, malware and ransomware4.monitor identity and access management, including monitoring for abuse of permissions by authorised system users5.liaise with stakeholders in relation to cyber security issues and provide future recommendations6.record all findings, actions taken and lessons learned following an incident to strengthen future responses7.generate incident reports for both technical and non-technical staff and stakeholders8.identify potential weaknesses and implement measures, such as firewalls and encryption9.investigate security alerts and provide incident response using incident handling methodologies and best practices10.Determines security violations and inefficiencies by conducting periodic audits.11.Upgrades system by implementing and maintaining security controls.12.monitor for attacks, intrusions and unusual, unauthorised or illegal activity13.test and evaluate security products and check suppliers certification, compliance and accreditation14.design new security systems or upgrade existing ones15.use advanced analytic tools to determine emerging threat patterns and vulnerabilities16.keep up to date with the latest security and technology developments17.Research/evaluate emerging cyber security threats and vulnerabilities and ways to manage them18.Plan for disaster recovery and create contingency plans in the event of any security breaches19.engage in 'ethical hacking', for example, simulating security breaches20.Contributes to team effort by accomplishing related results as needed.21. Troubleshooting security and network problems22. Responding to all system and/or network security breaches23. Participating in the change management process24. Testing and identifying network and system vulnerabilities25. Daily administrative tasks, reporting, and communication with the relevant departments in the organization. Mandatory Technical Expertise:1.Vulnerability Management tool Tenable / Nessus, WAS, Qualys, CrowdStrike, Burpsuite, Web Security Scanner2.XDR Platform Trend Micro and MS Defender3.Azure and Azure AD and Security tools, Defender EDR, Defender for Office, Defender for Cloud/Server/DB4.SIEM Trend Micro or FortiGate or IBM QRadar, Log Rhythm, MS Azure Sentinel (Azure Event Hub, Azure Log Analytics Workspace)5.Experience with Web filtering tool specifically with Fortinet, and NAC / Cisco ISE(a). Implement new web filtering solution using Fortinet(b). Test, verify and implement policies, create groups, grand access to groups. 6. Experience with WAF Imperva, FortiWeb, F5 7. Experience with DMARC RUA/RUF6.Experience with Firewall and Firewall rules, IP addressing, subnets, ports and VPN. (a). Configure and implement firewall rules(b). Audit firewall rules and network segmentation.(c). Verify and Submit firewall rule requests(d). Working Knowledge on OT firewall(f). Practical knowledge on Azure Firewall, VNET, NSG, VPC , CIPM configuration7.Significant Experience with SIEM to (a) Configure and implement rules, data sets, APIs, third party cloud API integration to facilitate ingestion of logs sources like o365, Azure AD, AWS(b) Integrate log data sets with SIEM(c) Configure IOC, and alerts(d) Conduct searches raw logs, Investigate alerts, assets, domains, users, IPs, files, Threat Intelligence and Threat Advisories (TI / TA)(e) Configure and monitor events using rules and run rules against historical data(f)Working experience with Python, Kali-Linux, YARA-L language8.Experience with AD, GPOs, Security groups, Windows Servers, Desktop OS.9.Experience in the field of Information Systems Security required. Analyst must have working knowledge of relevant ISO 27001/FISMA/NIST information security regulations and guidelines.10.Working knowledge of IT Security Best Practices regarding networks and networking including protocol analysis, anomaly detection, and troubleshooting11.Experience reviewing logs, scripting tasks, or creating structured queries/regex searches12.GxP, 21CFR and GMP Process knowledge is a plus13.Advanced understanding of TCP/IP, common networking ports and protocols, traffic flow, system administration, OSI model, defense-in-depth and common security elements.14.Hands-on experience analyzing high volumes of logs, network data (e.g. Netflow, FPC), and other attack artifacts in support of incident investigations15.Experience with vulnerability scanning solutions16.Proficiency with at least 4 or 5 of the following: Anti-Virus, XDR, SIEM, NIPS, HIPS, WAF, ID/PS, Full Packet Capture, Host-Based Forensics, Network Forensics, Encryption and RSA Security17.In-depth knowledge of architecture, engineering, and operations of at least one enterprise SIEM platform (e.g.Trend Micro, Microsoft Sentinel, ArcSight, QRadar, LogLogic, Splunk)18.Experience developing and deploying signatures (e.g. YARA, Snort, Suricata, HIPS)19.Understanding of mobile technology and OS (i.e. Android, iOS, Windows), VMware technology, and Unix and basic Unix commandsEducation, Experience, and Licensing Requirements:Bachelors Engineering degree in computer science, Information SystemsSecurity Analyst: 5-7 years of prior relevant experienceSenior Security Analyst: 8-10 years of prior relevant experienceAdvanced certifications such as CEH, CHFI, ECIH, CISM, SANS GIAC/GCIA/GCIH, CISSP or CASP and/or SIEM-specific training and certificationITIL Foundation or Intermediate ProcessCertified in CAPM or PMP or Prince2

Role & responsibilities Expertise in batch manufacturing and preparation related activities.To observe & follow all rules and regulations of the production department.Must be from Parenteral background & exposure to Aseptic vial / Bottle filling process is desirable.To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures.Technical exposure and expertise on filling & Autoclave machine.Exposure of USFDA audits.Preferred candidate profile Candidate should have relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization. Perks and benefits As Per Company Norms.