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.

Cyber Security Analyst 1. Planning, implementing, managing, monitoring, and upgrading security measures for the protection of the organizations data, systems, and networks 2. Ensuring that the organizations data and infrastructure are protected by enabling the appropriate security controls 3.monitor and respond to common cyber threats such as 'phishing' emails, 'pharming' activity, malware and ransomware 4.monitor identity and access management, including monitoring for abuse of permissions by authorised system users 5.liaise with stakeholders in relation to cyber security issues and provide future recommendations 6.record all findings, actions taken and lessons learned following an incident to strengthen future responses 7.generate incident reports for both technical and non-technical staff and stakeholders 8.identify potential weaknesses and implement measures, such as firewalls and encryption 9.investigate security alerts and provide incident response using incident handling methodologies and best practices 10.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 activity 13.test and evaluate security products and check suppliers certification, compliance and accreditation 14.design new security systems or upgrade existing ones 15.use advanced analytic tools to determine emerging threat patterns and vulnerabilities 16.keep up to date with the latest security and technology developments 17.Research/evaluate emerging cyber security threats and vulnerabilities and ways to manage them 18.Plan for disaster recovery and create contingency plans in the event of any security breaches 19.engage in 'ethical hacking', for example, simulating security breaches 20.Contributes to team effort by accomplishing related results as needed. 21. Troubleshooting security and network problems 22. Responding to all system and/or network security breaches 23. Participating in the change management process 24. Testing and identifying network and system vulnerabilities 25. 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 Scanner 2.XDR Platform Trend Micro and MS Defender 3.Azure and Azure AD and Security tools, Defender EDR, Defender for Office, Defender for Cloud/Server/DB 4.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/RUF 6.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 configuration 7.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 language 8.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 troubleshooting 11.Experience reviewing logs, scripting tasks, or creating structured queries/regex searches 12.GxP, 21CFR and GMP Process knowledge is a plus 13.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 investigations 15.Experience with vulnerability scanning solutions 16.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 Security 17.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 commands Education, Experience, and Licensing Requirements: Bachelors Engineering degree in computer science, Information Systems Security Analyst: 5-7 years of prior relevant experience Senior Security Analyst: 8-10 years of prior relevant experience Advanced certifications such as CEH, CHFI, ECIH, CISM, SANS GIAC/GCIA/GCIH, CISSP or CASP and/or SIEM-specific training and certification ITIL Foundation or Intermediate Process Certified in CAPM or PMP or Prince2

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 Lab Position - 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, Ahmedabad Interview 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 environment Note: - Ready to work in all shift are mandatory (first / second / general & night)

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 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activities OSD Manufacturing ( Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time and Venue : 05th April 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ 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

Job Title: Asst. Manager Operation Finance Greece Department : Finance Location : Ahmedabad Specific 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 clarification MIS & 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 skills Strong cultural awareness ensuring an ability to work with global colleagues Capable of working on own initiative Team player demonstrating maximum flexibility as required to complete key tasks Strong 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 constraints Flexible and thrive in fast paced, changing environment. Commercial outlook and ability to understand business priorities and challenges.

Function: Business Finance FP&A (Emerging Market) CA/MBA with ~ 6-10 years of experience. Brief Job role Review of Business case and agreements for In License products Support and Lead BPC project Analyzing the business model deployed by country Doing ROI analysis for investment Vis a Vis return from business Review in market inventory situation and prepare liquidation plan in consultation with country finance Monitoring of working capital and Monthly cash flow forecast Assisting business leader in various report / analysis for respective territory Any other critical Ad hoc projects Good In communication, Analytical Skill & Project Management.

Position Manager SAP ABAP Location Ahmedabad Note : This role we are looking for work from office only. DO ot have WFH or Hybrid facility. Roles & Responsibilities Work as ABAP Programmer Preparation 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 & Experience Qualification B Tech / M Tech / MBA / MCA Preference - Pharma work Experience and SAP Certification in ABAP 5+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

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

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 chemist Chemical Research & Analytical Research activities to be performed Hands on experience of instrument like HPLC & GC

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.

Skill Required: Aseptic operation Upstream/Downstream processing Cell culture/Microbial Knowledge 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.

Role & responsibilities Quality Control- RMPM

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.

GMP Upstream role KEY RESPONSIBILITIES Carries 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 gowning Prepares equipment and raw materials for manufacturing Performs (preparation and execution) aseptic process simulation (media fill) Executes all steps outlined in the batch records Reads and fulfils in real time production batch records and equipment logbooks Perform and assures the cleaning state and routinary maintenance of the manufacturing equipment Immediately 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 management Carries out the work in compliance with company Safety Policies Prepares for production (engineering batch, full scale batch, clinical batch) and identification of batch specific requirements Reports any accidents, incidents and injuries immediately notifying any hazards, unsafe procedures, or conditions in the workplace Keep up to date by participating in training courses and opportunities Participates at writing and revision of SOPs and Manufacturing documents Participate to the quality investigation from production side Participates at Regulatory Authorities audits for aspects pertaining the role Supports the activities for periodic qualification of clean room interacting with QA and engineering Is involved in process-related meetings Collaborates with Process Development team to bring manufacturing process in GMP Experience and Knowledge Experience in clean room environments Previous experience in fermentation and cell culture is mandatory Experience in manufacturing of any or all - plasmids, viral vectors, or Biologics GMP upstream is essential Experience 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 Qualifications BSc or MSc Degree or equivalent in Life Sciences or Biological / Chemical Engineering with 3-5 years of experience in cGMP setting.

GMP Downstream role KEY RESPONSIBILITIES Carries 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 gowning Prepares equipment and raw materials for manufacturing Performs (preparation and execution) aseptic process simulation Executes all steps outlined in the batch records Reads and fulfils in real time production batch records and equipment logbooks Perform and assures the cleaning state and routinary maintenance of the manufacturing equipment Immediately 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 management Carries out the work in compliance with company Safety Policies Prepares for production (engineering batch, full scale batch, clinical batch) and identification of batch specific requirements Reports any accidents, incidents and injuries immediately notifying any hazards, unsafe procedures, or conditions in the workplace Keep up to date by participating in training courses and opportunities Participates at writing and revision of SOPs and Manufacturing documents Participate to the quality investigation from production side Participates at Regulatory Authorities audits for aspects pertaining the role Supports the activities for periodic qualification of clean room interacting with QA and engineering Is involved in process-related meetings Collaborates with Process Development team to bring manufacturing process in GMP Experience and Knowledge Experience in clean room environments Previous experience in downstream purification is mandatory Experience in manufacturing of any or all - plasmids, viral vectors, or Biologics GMP upstream is essential Experience of any or all tasks including performing filtration, chromatography and associated techniques is essential 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

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 Validation To 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.

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 ASSURANCE IPQA (Injectable) - (Officer / Senior Officer / Executive) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY ASSURANCE (QMS / Compliance / Documentation/ Validation & Qualification/OSD) (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. Engineering: Instrumentation / QMS (Senior Executive / Executive / Senior Officer) Experience - 03 to 09 Years Qualification 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 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activities OSD Manufacturing & Packing ( Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time 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

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 System Position - 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 Facility Date : 15th March 2025 Department - 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