Job description:Providing Line Clearance to the equipment's and areas. Issuance of documents as per procedures. Review of all online documentation activities.To monitor the cGMP at the shop floor periodically. Monitoring process validation activities of various products. Review of GMP records and ensuring compliance for any observations. Responsible for coordinating self-inspection. Assist in deviation, incidence, OOS/ OOT investigations.Awareness in guidance on ICHQ7Candidates with less than 1 month notice period or immediate joiners will be preferred.

Position: Executive/Assistant Manager - MDMLocation: Hinjewadi Phase 1Experience: 5-6 YearsKey Responsibilities:Master Data Creation: Hands-on experience in creating and managing SAP master data, including Material Codes, Vendor Codes, Customer Codes, Bill of Materials (BOM), and Recipes.Solution Design: Develop and implement SAP MDM solutions tailored to business requirements.Data Management: Build and maintain MDM repositories, ensuring data accuracy and consistency.Data Integration: Facilitate data load and syndication processes, ensuring seamless integration with other systems.Workflow Development: Create and manage MDM workflows, including de-duplication, validation, and data quality checks.Testing and Documentation: Perform unit tests, support integration tests, and complete project documentation.Client Interaction: Collaborate with business stakeholders to understand requirements and provide MDM solutions that meet their needs.Compliance: Ensure all MDM processes comply with Good Manufacturing Practices (GMP) and other regulatory standards.Data Governance: Develop and enforce data governance policies and procedures to ensure data quality and consistency. Establish data stewardship roles and responsibilities and monitor compliance with data governance standards.Qualifications:Education: Bachelors degree in computer science, Information Technology, or a related field.Experience: 5-6 years of experience in SAP MDM, with a focus on pharmaceutical manufacturing.Technical Skills: Proficiency in SAP MDM, data modeling, and data integration tools. Soft Skills: Strong analytical and problem-solving skills, excellent communication and documentation abilities, and the ability to work collaboratively in a team environment.Regulatory Knowledge: Familiarity with GMP and other regulatory requirements in the pharmaceutical industry.Preferred Qualifications:Experience with data governance and data quality management.Certification in SAP MDM or related fields.Previous experience in a similar role within the pharmaceutical manufacturing sector.If interested, pls share your updated cv.

About the Company:Emcure Pharmaceuticals is an Indian multinational that specializes in manufacturing generic pharmaceuticals and active pharmaceutical ingredients (APIs). Founded in 1983, it has grown into a significant player in the global pharmaceutical industry, focusing on Gynaecology, Oncology, Cardiology and Anti-Infective therapies. Emcure is known for its commitment to innovation, quality, and affordable healthcare solutions worldwide.About the Role:The Zonal Manager is responsible for generating income by developing the strategy and business plan for sales growth in his/ her zone and works to implement it at the ground level by directing, inspiring, and motivating his/her team members to generate more sales by convincing doctors to prescribe their drugs to patients. Locations: Mumbai, Hyderabad, Vijaywada, Therapy: Gynecology, IVF, OrthopedicRoles & Responsibilities:Sales Management:Consistently achieve the zones targets.Identifying & meeting the Top KOLs, KBLs.Inventory management and track the trend of demand.Track performance of teams and allocate available resources.Tracking the New Product Introduction ( NI) movement across zones. Ensure that all TMs and RMs are on > 100%Track & monitor sales progress across zones.Process Orientation:Check call per day, coverage & compliance of TMs and RMs and of all HQs as per the company norms.Checking the implementation of RCPA during JFW to know the competitors better.Submission of accurate and timely reports by all team members.Streamline processes within the team eg: Maintain timelines, establish proper ways of working.People Development:Coach & guide RMs and TMs on their strengths & areas of improvement.Provide performance feedback based on observation in joint calls.To explore new growth opportunities across the zones for better utilization of allocated manpower.Be updated with business information and provide information to team on recent developments.Provide team member platforms to voice their concerns and adequate solutions.Connect with Internal Stakeholders to address people related issues.Market Development:Capture market feedback from customers (internal and external) on a regular basis and provide inputs to PM team.Meet and maintain good relations across top key stakeholders of the zone.Developing a potential customer data base and initiate activities to create a regular prescriber base.Qualification: Graduate, ideally in a Science or Pharmacy discipline Minimum 8 Years of total experience, 3 Years of team handling

Designation: Senior Manager - Europe MarketExperience: 10-15 YearsReporting: Head RAQualification: B.Pharm/M.PharmJob Location: PuneTeam handling experience: 4-6 membersDosage form: All types1. Strong experience in Regulatory Affairs for Europe market.2. To build regulatory strategy for submission of initial MAA for EU (DCP/MRP/NP/CP), evaluation of changes and maintenance of product life-cycle for different dosage forms.3. Compilation of dossiers in CTD, eCTD & national formats for Europe4. Compilation and submission of queries and variations.5. Regulatory compliance with Front offices and with Plant.6. Review of documents, artworks7. Review of change controls8. Gap analysis for new product filing9. Maintaining product Life cycle10. Liaise with all cross functional departments for evaluation/approval of change proposal/deviations/escalation and their execution.11. Internal guidance document preparation.12. Work allocation to subordinates with tracking and review of tasks.13. People management- Responsible for training and development of team.Looking forward for candidates having strong experience in Europe market and capable of leading a team.If relevant and interested pls share your profile.

Maintenance of equipments of granulation area like FBD,RMG, multimill, sifter, blenders, cad mills etc.Maintenance of compression machines (Cadmach/ Korsch /ACG make), metal detectors, lifting and positioning devicesMaintenance of capsule filling machine and line equipment’s.Maintenance of coating machines (NEO MACHINE make), stirrers, colloid mills.Maintenance of Blister packing, cartonators, checkweigher, track and trace system etc.Maintenance of bulk packing lines.Facility, lux level measurement, RA measurement.Handling of documents (PM, lux, RA, etc.)SAP knowledge

Open Positions 1. Utility Officer 1. Instrument Officer 1. Electrical Officer 1. QMS -DocumentationTo Ensure Utilities Maintenance/Instrumentation/Electrical & Operation, QMS Activities as per industrial standards and bench mark. Maintain the Equipment for achieving Efficiency , reliable Operation and in line with Pharmaceutical requirement following Good Engineering Practices Qualification B Tech / Diploma in Electrical Engineering Experience: 03-07 Years

Operator for Liquid ManufacturingWith Experience of Liquid manufacturing activity.Track & Trace Bar CodingCarton CodingSticker Labeling MachineGood GDP and GMP knowledge-logbook .

To perform analysis of finished Products and in-process samples. Proficiency in using analytical instruments such as UV/VISIBLE and IR, HPLC Handling of laboratory incidents and deviation. Extensive knowledge of GMP regulations in cGMP Manufacturing Environment. Chemical and Instrumental analysis of In process and finished products. To perform analysis of stability samples. To perform the calibration of instruments like HPLC, Dissolution tester, UV Spectrophotometer. Analysis of OOS/OOT

Responsible for handling production packing lines Responsible for cGMP during production activityResponsible for In-Process analysis in Shifts (as per the instruction mentioned in BMR & BPR)Ensure training, master batch records, SOPs and other documents are current and compliant under cGMPHanding ManpowerResponsible for daily Production activities as per production planning

Urgent hiring!!!!! Location: Sikkim Department: Quality Control Designation: Officer/Sr. Officer Preferred candidate - Having 3 - 5 yrs. of experience in Quality control - FG/RM section Must have hands on experience in QC instrument i.e. HPLC, UV Spectrophotometer, FTIR, K.F apparatus, Analytical balance, pH meter, Water Activity Analyzer. Candidate from OSD only.Interested candidate may apply at hr.plant@zuventus.com Preference will be given to early joiner.

Water sampling and testing, Manufacturing and Sterility areaMedia PreparationEnvironmental Monitoring Swab Analysis Microbial Limit TestAutoclave handing Analytical Method Validation for Raw Materials

HR GENERALIST POSITION Talent Acquisition, handling Recruitment and On boarding Cycle Identifying talent needs, develop workforce plans, and implement strategies for talent acquisition, retention and development Good Communication/Spoken Skills Managing employee relation issues and providing guidance on corrective actions. Maintained MIS and employee files and records Statutory & HR-GMP Compliances Manpower Handling

IPQA SPECIALIST

Preparation and review of SOPs, BMR/BPR.To process Change control and Deviations. Proficient in handling Track wise To initiate Change Control, CAPA, Deviation, Risk assessment, Market complaint, Investigation To update and maintain Index of SOPs and Formats.To issue & Retrieve Logbooks, Formats etc. To assist in compliance for internal and external audits On line training module knowledge.Should have good knowledge & proficiency in Computer. Must have worked in QMS of reputed Pharmaceutical industry Awareness of internal and external audit dealing is required Regulatory plant experience

Job Description:Candidate will be based at PUNE and will be responsible for New Vendor qualifications for APIs/Excipients required for Finished Pharmaceutical Products.1. Graduate BSc/B Pharm having 3-6 yrs of experience in Pharmaceutical Purchase Function (Raw material API & Excipients)2. Knowledge of Regulatory requirements of RM for different Countries like US/Europe/Canada/Emerging market3. Candidate should have basic knowledge of SAP/HANA4. Negotiations with Vendor and placing Purchase Orders5. Follow up with Vendors to ensure timely supply for alternate/New Vendor development of APIs/Excipients (Indian/Import)6. Handling of request/queries from Internal customers like Formulation Development (F&D), Analytical, QC/QA , RA to Vendor and obtains timely response.7. Arranging of all related documents for Vendor qualifications, submission to Regulatory & keep records of the same

We have opportunity in Regulatory Affairs for Emerging MarketsPosition: Officer/Executive Regulatory AffairsExperience: 2-5 YearsQualification: B.Pharm/M.PharmLocation: Pune Compilation of dossiers in CTD, eCTD & national formatsCompilation and submission of queries and variations.Review of documents, artworksReview of change controlsGap analysis for new product filingMaintaining product Life cycle Candidates having experience LATAM/CIS/ Africa or any other Emerging Markets can applyIf relevant and interested, pls apply

Job DescriptionCompany: Emcure Pharmaceuticals Ltd.Role: Officer/ExecutiveDepartment: Network and SecurityLocation: Hinjewadi, Pune.Role and ResposibilitiesPrimary Skill: Cisco SwitchesCisco RoutersSDWAN VmWare VelocloudWIFI RuckusSecondary skill: Firewall: Checkpoint / Palo Alto, PanoramaGood understanding of TCP-IP, UDP, OSI model, DHCP, DHCP relay, DNSStrong experience in Cisco Routing and Switching, Cisco nexus, Cisco Prime, Network monitoring tools.Good troubleshooting skill in Switching, STP, L2 switching, VTP, VLAN, IP subnetting.Good experience of port security, DHCP SnoopingGood experience of Telnet, SSH, HTTP, HTTPS, console, and TACACS+/RADIUSWork experience with access control, ACLs, VPNsKnowledge of VmWare, VeloCLoud SDWAN, WAN QOS, Good experience in Network and security operations.Proactively grab KT from client.Help and guide junior team membersProvide support to project managers on security/network projects and deploymentsSolid advanced technical skills related to infrastructure technologies including but not limited to Cisco Local Area Networks (LAN) and Wide Area network (WAN) routers and switches, Wireless, Cisco Nexus platform.Good working experience on Cisco Nexus, VDC, VPC, Cisco VXLAN, Cisco catalystGood working knowledge on Ruckus Wireless and Wired network.Solid advanced technical skills on Routing protocols like BGP, EIGRP and OSPF etc.,Solid advanced technical skills on HSRP, STP, VTP, Nexus OTV and Fabric Path,Good troubleshooting knowledge on VeloCloud SD-WAN.Knowledge on packet captures tools like Wireshark and analysis.Good knowledge on Network monitoring and management tools (NetFlow, SNMP).Good working knowledge on QOS.Certification requirements – CCNA, CCNP preferred, CCIE is value add.Note* Candidates having NSE 4 certifications are preferred.

Proactively contribute in Project Initiation, execution, Tracking, Monitoring, Troubleshooting and Facilitating activities till dossier filing. Accountable for the overall outcome of the project from Initiation to Completion.Closely work with US, EU, CA, ROW, Brazil Project managers ,Bridge between R&D and different territory Project managerContribute to Project Initiation in Tool , Project budget preparation. Track and monitor actual vs. budget (cost, man-hours, material) for their optimum utilizationTo ensure R&D sourcing and Supply chain for API (IH & OSC). RLD, RM/PM, Equipment availability for R&D and Plant, BE studies (CROs) and prioritizing on projects. Provide necessary inputs for initiating the procurement process. Track, review & regulate the progress of the project to meet the deliverables. Compare target, planned and actual (Schedule/cost/quality), report the variance to stakeholders, Identify scope change in cost, schedule, facilitate on necessary approvals. Active participation in Annual Budgeting for R&D, and quarterly reviewing the BE budget of budget vs. actual costing and number of studies.Work closely with Plant TT, Plant QA, and QC for production schedule, monthly, quarterly and annual plans for manufacturing of R&D batches. Track RM release, AMV and TT, Micro validation leading to manufacturing of submission batches at OSD and Sanand.Track deficiency for solid orals and coordinate the priority for different analytical activities leading to deficiency response submission by RA for OSD and Sanand Use of appropriated tools to plan and execute projects from timelines, cost and quality perspective. Conduct timely meetings to keep track of ongoing projects and meet deliverables.PM Initiatives: Contribute in implementation of new initiatives in PM department, Coaching team members on Project Management practices.Planning tracking, monitoring and review of the execution of the batches at manufacturing sites OSD and Sanand, conducting weekly meeting to ensure the smooth functioning and availability of the requirements for batch execution. Compilation of Project closure report on completion of the project, implementation of project management tool for monitoring like variance analysis on timely basis.

Role: Regulatory Affairs CanadaJob location: Pune, WakadExperience: 1-4 YearsJD:1. Experience in Canada market is required2. Involved in Dossier preparation, Submission, Compilation of NDS/ANDS, Query Response for all dosage forms.3. Modulewise documents review in line with eCTD guidelines4. Responses for screening deficiencies.5. Gap Analysis 6. Should have good knowledge and understanding of ICH and ANDS guidelines.7. Hands on experience for review of various documents such as specifications, method of analysis, analytical method validations, product development reports, stability protocols etc.8. Knowledge of DocuBridge software is preferred.If relevant and interested, pls share your resume

Therapy: Paediatric, Physician (General Segment), Gynaecology.Position: MREligibility Criteria: B. Sc/ B. Pharma/ B. Com with 3 to 5 years of Pharma Experience in respective therapy.Age: Upto 30 years.Key Responsibilities:Ensure desired visits to Doctors, Chemist, Stockiest and drive secondary sales. •Maintaining proper Call Average, coverage & frequency as per the company norms. •Generate prescriptions from doctors by providing scientific information about the products and explaining the benefits to the patients. •Meeting retail chemists/ purchase heads to make sure that the company products are easily available for patients. •Meeting authorized Distributors/ Stockiest to ensure the required inventory. •To analyze monthly sales trend and have an action plan for SKU wise growth. •To enhance span of prescribers and prescriptions with available doctors list. •To execute marketing strategies and build the customer base to improve sales numbers. •To ensure on-time submission of DCR, stock statement and expense statement, etc. •Follow-up instructions from seniors about shortfalls as well as action plan to surpass monthly targets. •Keeping a close eye on competitor brands and detail to the doctor about unique selling point for our brand.Interested Candidates Kindly share your CVs with Sumit.Sharma1@emcure.com

Walk-In Drive - API- Quality Walk-in Interviews for API - Quality Roles based out of Kurkumbh (Job location) on 06 & 07 April, '2025 (Sunday& Monday), from 1000hrs. to 1600 hrs. at Kurkumbh, MaharashtraWe have the below openings:API - Quality Control :M.Sc. (Analytical / Organic Chemistry) with 2-5 years experience withExpertise in handling RM, intermediates & Finished products in API manufacturing.Handling HPLC, GC, LCMS, ICPMS.Knowledge of Particle Size Analyzer/LCMS /GCMS preferred API - Quality Assurance:M.Sc. (Organic Chemistry) BE/B Tech (Chemical Engineering) with 2-5 years of experience with Must have experience only in API. Experience in API Inprocess QA, API line clearance , QMS, APQR, Process & Cleaning validations will be desirable.Experience of API production as well as QA will be preferred.

Therapy: Paediatric, Physician (General Segment), Gynaecology.Eligibility Criteria: B. Sc/ B. Pharma/ B. Com with 3 to 5 years of Pharma Experience in respective therapy.Age: Upto 30 years.Key Responsibilities:Ensure desired visits to Doctors, Chemist, Stockiest and drive secondary sales. •Maintaining proper Call Average, coverage & frequency as per the company norms. •Generate prescriptions from doctors by providing scientific information about the products and explaining the benefits to the patients. •Meeting retail chemists/ purchase heads to make sure that the company products are easily available for patients. •Meeting authorized Distributors/ Stockiest to ensure the required inventory. •To analyze monthly sales trend and have an action plan for SKU wise growth. •To enhance span of prescribers and prescriptions with available doctors list. •To execute marketing strategies and build the customer base to improve sales numbers. •To ensure on-time submission of DCR, stock statement and expense statement, etc. •Follow-up instructions from seniors about shortfalls as well as action plan to surpass monthly targets. •Keeping a close eye on competitor brands and detail to the doctor about unique selling point for our brand. Interested Candidates Kindly share your CVs with Sumit.Sharma1@emcure.com

Company: Emcure PharmaceuticalsTherapy: Paediatric, Physician (General Segment), Gynaecology.Position: MREligibility Criteria: B. Sc/ B. Pharma -FresherB.Com with 1 year of experienceAge: Upto 30 years.Key Responsibilities:Ensure desired visits to Doctors, Chemist, Stockiest and drive secondary sales. •Maintaining proper Call Average, coverage & frequency as per the company norms. •Generate prescriptions from doctors by providing scientific information about the products and explaining the benefits to the patients. •Meeting retail chemists/ purchase heads to make sure that the company products are easily available for patients. •Meeting authorized Distributors/ Stockiest to ensure the required inventory. •To analyze monthly sales trend and have an action plan for SKU wise growth. •To enhance span of prescribers and prescriptions with available doctors list. •To execute marketing strategies and build the customer base to improve sales numbers. •To ensure on-time submission of DCR, stock statement and expense statement, etc. •Follow-up instructions from seniors about shortfalls as well as action plan to surpass monthly targets. •Keeping a close eye on competitor brands and detail to the doctor about unique selling point for our brand.Interested Candidates Kindly share your CVs with Sumit.Sharma1@emcure.com

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities:Outline the day-to-day responsibilities for this role.Preferred candidate profile:Specify required role expertise, previous job experience, or relevant certifications.Perks and benefits:Mention available facilities and benefits the company is offering with this job.