Alembic Pharmaceuticals is a leading pharmaceutical company with a strong emphasis on research and development (R&D). The AGM / Deputy General Manager (DGM) of Project Management in the R&D department at their Hyderabad location plays a pivotal role in overseeing and coordinating various projects to ensure they align with the company's strategic objectives. Key Responsibilities:Project Planning and Management: Define project scopes, objectives, and deliverables in collaboration with senior management and stakeholders. Develop detailed project plans, including timelines, resource allocation, and budget management. Coordinate and lead project team meetings to ensure alignment on project goals and milestones.Execution and Monitoring: Oversee day-to-day project activities, ensuring adherence to project plans and schedules. Monitor project progress, identify potential risks and issues, and implement mitigation strategies. Track project performance using appropriate systems, tools, and techniques.Stakeholder Communication: Serve as the primary point of contact for project stakeholders, including internal teams, external partners, and regulatory authorities. Prepare and present regular project updates to senior management. Foster strong relationships with stakeholders to ensure project alignment and support.Qualifications and Experience:Educational Background: A Master's degree in Pharmacy, Chemistry, or a related field is typically required. An MBA or equivalent management qualification is advantageous.Experience: A minimum of 10 to 18 years of experience in project management within the pharmaceutical industry, with a focus on R&D projects.Technical Skills: Strong understanding of pharmaceutical R&D processes, regulatory requirements, and quality standards. Proficiency in project management tools and methodologies.Soft Skills: Exceptional analytical, strategic thinking, and problem-solving abilities. Excellent communication and interpersonal skills, with the capability to influence and collaborate at all organizational levels.Interested candidates can share CV on bdcv@alembic.co.in

Alembic Pharmaceuticals Ltd is looking for a Regulatory Affairs professional for the position of Senior Executive/Assistant Manager/ Deputy Manager based at our Corporate Office - Vadodara, Gujarat. Job Criteria:B.Pharm or M.Pharm qualification having experience between 7 - 15 yrs. with dossier filling experience in MEXICO or South East Asian Countries. Knowledge for review of quality documents like executed batch documents, method validation, change Good communication skill Job Responsibility:Compilation and review of product license applications, variations, and renewals for Mexico country as per regulatory requirements respectively with minimal supervision Manages electronic documents and creates electronic submissions in CTD format. Preparation and review of responses to authority questions during registration and product lifecycle. Keep track of assigned projects and follow-ups to ensure the Dossier is delivered as per set timeline/commitments. Designing, Reviewing & Approval of Artwork required for registration purposes. •Dossier due diligence for products being in-licensed from other company Support in preparing the meeting materials as needed, eg, regulatory project status/ submission/ approval information monthly, quarterly or yearly. Interested professionals may share their CVs to janihimanshu@alembic.co.in stating position code RA-MEXICO” in subject line

Role Significant experience managing operations in Southeast Asian Markets such as Vietnam, Thailand, Philippines, Malaysia, and Hong Kong,Should demonstrate a strong understanding of B2B business dynamics and have independently managed and traveled across these regions. A solid grasp of business contracts, along with excellent negotiation skills, is essential. They should also have a fair understanding of the regulatory frameworks in these markets. Any exposure to B2C business would be an added advantage. Key Skills & Experience Experience: 8+ years in business development, with at least 3 years focusing on Southeast Asia markets.Skills:Strong negotiation and deal-closing abilities.In-depth knowledge of South East Asias cultural, economic, and regulatory landscape.Excellent communication and relationship management skills. Core Responsibilities Strategic PlanningDevelop and execute regional business development strategies aligned with corporate objectives.Identify and evaluate new market opportunities within South East Asia.Market ExpansionEstablish and maintain strong relationships with clients, partners, and stakeholders in the region.Drive partnerships, joint ventures, or acquisitions to expand market share.Revenue GrowthAchieve revenue targets and sales quotas through effective account management and lead generation.Collaborate with sales, marketing, and product teams to design offerings tailored to local markets.Market AnalysisConduct market research to understand trends, competition, and customer needs in the region.Provide actionable insights to influence product positioning and pricing.LeadershipLead and mentor a team of business development professionals.Represent the organization at conferences, trade shows, and networking events.

Role & responsibilities 1. Maintenance activities (Preventive and breakdown) related to plant equipments.2. Maintaining records related to GMP, GEP 3. Execution of activities related to Plant modification & product change over. 4. Ensure Plant Modification Projects are carried out smoothly and effectively as per written procedures.5. Issue of materials from engineering stores on need basis.6. Measurement & verification of bills of contractors.7. Co-ordination with other interfacing departments.8. To ensure that all the activities at the site are carried out as per GMP/SOP.9. Preparation of SOP, giving training to staff / technicians, ensure continuous training of the workmen to keep them up to date with latest GEP.10. Surface area calculation for plant equipments on need basis.11. Preparation of P&ID with help of draftsman.12. Maintaining documents as per SOP.13. Implementation of key new initiative / project

1. Warehouse Operations & ComplianceOversee daily warehouse activities, ensuring proper receipt, storage, and dispatch of APIs and raw materials.Ensure strict compliance with GMP, GDP, FDA, MHRA, EMA, and other regulatory requirements.Maintain documentation as per pharmaceutical industry standards (SOPs, batch records, and audit logs).Conduct regular audits and inspections to ensure adherence to QA/QC standards.Implement and maintain temperature-controlled storage and handling of APIs.2. Inventory & Supply Chain ManagementMaintain accurate inventory records using ERP/WMS systems (e.g., SAP, Oracle, or equivalent).Monitor stock levels to prevent shortages or overstock situations.Implement and improve inventory tracking systems to reduce errors and inefficiencies.Coordinate with procurement, production, and distribution teams for seamless supply chain operations.3. Team Leadership & DevelopmentLead, train, and mentor warehouse staff to ensure high productivity and compliance.Develop training programs focused on GMP, safety, and warehouse best practices.Foster a culture of continuous improvement and adherence to safety protocols.4. Safety & Risk ManagementEnsure compliance with OSHA, EHS (Environmental Health & Safety) regulations, and hazardous material handling standards.Implement warehouse safety programs, including fire safety, spill management, and emergency response.Regularly assess warehouse risks and take preventive actions.5. Logistics & Distribution ManagementOversee the dispatch of raw materials and APIs, ensuring secure and timely delivery.Collaborate with logistics partners to optimize shipping and reduce costs.Monitor and improve warehouse layout and storage systems for operational efficiency. Key Requirements & Qualifications:Education: Bachelor's or Master's degree in Logistics, Supply Chain, or a related field.Experience: 15+ years in warehouse management in the pharmaceutical/API industry.Strong knowledge of GMP, GDP, and regulatory compliance.Proficiency in ERP/WMS systems (e.g., SAP, Oracle).Experience with temperature-sensitive pharmaceutical storage and distribution.Excellent leadership, communication, and problem-solving skills.Knowledge of ISO 9001,ISO13485, FDA, and EHS regulations.

Role & responsibilities Reporting of Unsafe Act & Unsafe conditions on daily basis.Follow the Work Permit System procedure and issue the work permit on daily requirement.To conduct and monitor the safety talk records along with HSE representative.Emergency communications as per On Site Emergency PlanEngage actively in accident and incident investigations, ensuring that corrective and preventive actions (CAPA) are promptly implement.To conduct the internal safety audits and various facility inspections and tracking the recommendation complianceTo conduct and participate in mock drills.Conduct on the job training, classroom training on Safety & Health topicsHIRA & JSA of critical activities to be conductedShould aware on the legal requirements based on various acts and rule, Maintain legal documents and ensure complianceHaving basic knowledge of chemical hazards and Material Safety Data sheet.To conduct departmental safety committee meetingsTo response emergency situation and follow On-site emergency plan.Conduct safety meeting with contract worker and supervisors.Ensure healthiness of Fire Protection and detection system.To monitor the Fire team and OHC team activities during shiftEnsure the healthy condition of fire protection and detection system

Role & responsibilities Systematic Plant Round Of Respective Areas To Identify Unsafe Act / Unsafe Conditions/ Unsafe Practices To Minimize Incidents.Ensure the Work Permits Procedure and safety related activity.Ensure Administrative Management of Occupational Health Centre (OHC).Ensure Effective Operation and Monitoring Of ETP , STP And Waste Management (Hazardous & Non Hazardous) As Per Statutory Requirement.

Dear Candidate,We are pleased to invite you to a walk-in interview for the position of Production Executive Details are mentioned below.Qualifications:- B.Sc./M.Sc./ B.E - B.Tech (Chemical Engg.)- 1 to 9 years of experience. - Experience in handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc.The interview will be held on :Venue - Alembic Vidyalay, Opp. Bhailal Amin General Hospital, Alembic- Gorwa, Vadodara, Gujarat - 390003Please bring a copy of your resume.During the interview, we will discuss the job requirements and your qualifications, and answer any questions you may have about the company and the position. We encourage you to be prepared and dress professionally.We look forward to meeting you and discussing this opportunity further.

Job Summary:We are seeking a highly skilled and result-driven AGM/DGM of API Manufacturing to lead and optimize our production operations. The ideal candidate will have extensive experience in API manufacturing, a strong understanding of cGMP and safety standards, and proven leadership capabilities in managing large teams.Key Responsibilities:Production Planning & Execution: Develop and implement effective production plans, ensuring seamless operations while optimizing resource utilization.Process Improvement & Compliance: Lead initiatives for process enhancements, efficiency improvements, and compliance with the latest cGMP and safety regulations.Resource & Team Management: Mobilize and manage manpower, equipment, and raw materials to ensure smooth plant operations.Cost Optimization: Implement control measures to maintain operational expenses within budgetary norms.Process Control & Waste Reduction: Define norms for raw material consumption and introduce control measures to minimize wastage and enhance productivity.Regulatory & Quality Compliance: Oversee investigations, deviations, change control processes, and SOP revisions in compliance with industry standards.Leadership & Strategy: Drive a high-performance culture by mentoring and guiding teams to achieve operational excellence.Key Skills & Competencies:Strong leadership and managerial capabilitiesExpertise in API manufacturing processesSound knowledge of cGMP, safety standards, and regulatory requirementsProblem-solving and decision-making skillsAbility to drive process efficiency and cost optimizationEffective communication and stakeholder managementPreferred Qualifications:Experience in handling large-scale API manufacturing unitsExposure to regulatory audits and quality management systems

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in SEA markets position based at Corporate Office Vadodara.Job Criteria: B.Pharm / M.Pharm / Any other science stream. Candidates with management degree will be given preference.10 + years in business development, with at least 3 years focusing on Southeast Asia markets.Significant experience managing operations in Southeast Asian Markets such as Vietnam, Thailand, Philippines, Malaysia, and Hong Kong.Should demonstrate a strong understanding of B2B business dynamics and have independently managed and traveled across these regions.A solid grasp of business contracts, along with excellent negotiation skills, is essential.They should also have a fair understanding of the regulatory frameworks in these markets.Any exposure to B2C business would be an added advantage.Strong negotiation and deal-closing abilities.In-depth knowledge and have established contacts in most of SEA countries cultural, economic, and policy.Interested applicants can share profile at bdcv@alembic.co.in with the job title "BD-SEA" in the subject line.

JOB RESPONSIBILITIES :[A] Regulatory Compliance :1. To co-ordinate with corporate regulatory department for submission of documents as part of filing of DMF, updating and response to queries to US, Europe, China, Japan, Korea and Rest of World market.2. To co-ordinate with various department for the timely submission of documents and its compliance.3. Coordination with quality control, analytical development lab (ADL) and corporate validation Lab (CVL) for specification and standard test procedures.4. Coordination with CQA for document preparation and implementation.5. Keep the track of technology/Analytical Method transfer and other documents received from ADL and R&D.6. Responsible for co-ordination during regulatory inspections and customer audits. Responsible for co-ordination with all stake holders for appropriate action plans for the corrective and preventive actions (CAPA) and timely closure.7. Review and approval of stability summary report and handling of stability failures. Responsible for timely communication with corporate regulatory department on the stability failures for further actions with regulatory agencies and customers.8. Responsible for the co-ordination with QC and other agencies for the timely qualification of working reference standards (WRS) of APIs, intermediates and impurities.9. Responsible for the management of Skip Testing and associated documents.10. Responsible for ensuring compliance of products against monograph specification.11. Review and approval of analytical raw data before the regulatory submissions for filing. [B] Validation.1. Responsible for review and approved of Process Performance Qualification protocols and reports through Documentum system.2. Responsible for review and approved Cleaning Validation and Verification protocol and report through Documentum system.3. Ensure compliance of validation master plan. A. Batch release and Dispatch: 1. Responsible for batch release, Certificate of analysis and material dispatch related activities.2. Responsible to communicate the business development and PPIC in case of any delays in the dispatches due to any reasons.B. QMS: 1. Responsible for Handling of Market complaint, returned goods and Recall activities.C. Product review:1. To ensure preparation, review & approval of Annual Product Quality Review (APQR) as per scheduled timelines in coordination with other departments. D. Audit and Compliance:1. Responsible for audit preparation, compliance and response to regulatory and customer.2. Responsible for Retain sample management of APIs & Saleable Intermediates. 3. Perform internal audits within Alembic site.E. Customer Support/ Compliance:1. Co-ordinate with Production, QC, supply chain, logistic, purchase and Marketing department for dispatch related activities and customer queries.2. To support the business development team during the development of new customers by providing required information as part of questionnaire assessment and Technical quality agreement.3. Coordination with quality control for specification, standard test procedures and QC related queries generated by customers.4. Handling of CAPA & Change control activities for implementation, monitoring and assessment.5. Review and approval of documents in DCS/Documentum.6. Any other task assigned by QA Head.

Role & responsibilities This position is accountable for - Providing product related technical /scientific information along with services (if any) to external clients like (Veterinary practitioners, consultant, Key accounts and para veterinarians) Extend regular support to conduct clinical/demonstration study related to product portfolios/marketing campaign/new launches and provides regular update to Marketing and Veterinary Services team Regular coordination with Veterinary Institution/Licensing authority (If any) to enhance the corporate image Deliver CVEs to Veterinary Institutions/Clinicians/Consultants/Dairy cooperatives/Dairy Farmers/Pet Parents etc.Write product related papers & popular articles in journals & technical articles Provide product related technical training/on job product training to field colleagues

Role & responsibilities 1. Maintenance activities (Preventive and breakdown) related to plant equipments.2. Maintaining records related to GMP, GEP 3. Execution of activities related to Plant modification & product change over. 4. Ensure Plant Modification Projects are carried out smoothly and effectively as per written procedures.5. Issue of materials from engineering stores on need basis.6. Measurement & verification of bills of contractors.7. Co-ordination with other interfacing departments.8. To ensure that all the activities at the site are carried out as per GMP/SOP.9. Preparation of SOP, giving training to staff / technicians, ensure continuous training of the workmen to keep them up to date with latest GEP.10. Surface area calculation for plant equipments on need basis.11. Preparation of P&ID with help of draftsman.12. Maintaining documents as per SOP.13. Implementation of key new initiative / project

Role & responsibilities 1. Operation supervision of ETP, STP, RO, Stripper, Multi Effect Evaporator, and MBBR Plant.2. Management of Hazardous waste generated from process and non-process areas.3. Operation of GPCB XGN system.4. Adjust the manpower of the shift as instructed by the Assistant Manager.5. Continuous follow-up for the maintenance work of the ETP, STP, RO, Stripper, Multi Effect Evaporator, and Incinerator Plant.6. Taking rounds in the production area to reduce unwanted waste water generation.7. Report all observations of operational activity to the Assistant Manager.8. Plant Safety Inspection & Execution and initiating work permit.9. Providing necessary assistance/Data for compliance concerning GPCB.

Role & responsibilities 1. Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development and any analysis allocated by team leader and release with proper documentation..2. Ensuring analysis is performed compliance to GLP.3. Ensuring analysis raw data is documented on-line.4. Initiation, Completion and filing of Daily analysis reports.5. Ensuring any abnormal results, incidents, deviations, discrepancies are reported immediately to the reporting Section Head.6. Ensuring all relevant log entries are made for every activity wherever applicable.7. Supervise compliance to all cGMP, GxP or any other regulatory requirements including EHS requirements.8. Report any quality concerns or suggestions for improvements to Department Head.9. Execute and supervise all tasks and activities as per the applicable SOPs and company policy.10. To maintain the safety norms while working in lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure etc).11. Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards.12. Ensuring self-discipline with respect to wearing aprons, attendance and personnel hygiene and inter relations.13. To perform Labware LIMS related activities.14. Any other assignment given by the Section Head or Department Head.

Job Responsibilities:Comprehensive pharmaceutical sales and marketing experience including, meeting doctors, chemists and managing the distributors.Responsible for achieving primary as well as secondary targets month after month for the HQs assignedAdept in implementing sales and marketing activities and accelerating the business growth.Monitoring sales team performance, analyzing sales data, periodical forecasting and reporting to Regional and Zonal heads.Present technical information clearly, concisely, and persuasively to customers.Develop and manage efficient distribution network for sales.Managing, training, motivating and developing existing sales team to drive revenue growth.Essential Skills required:Good communication skillsGood analytical and problem solving skillsStrong interpersonal skillsAdaptability to work at any environment

Product Selection/Opportunity IdentificationReview of patent & non-patent product literature to support product selection,Preparing & analyzing IP landscape to come up with launch scenarios and IP strategiesEvaluation of possible invalidation grounds of identified patents Product Development Support Formulation evaluations and IP clearancesSuggesting IP driven formulation approaches to R&D teamIP updatesMonitoring new/pending patent families/grants and timely updating changes in IP situationMonitoring pending litigation/new litigations and updating their influence on product development or launch Business Development SupportProvide possible launch dates based on IP situation for different markets,Provide response to customers during IP diligencePatent drafting, filing & ProsecutionEvaluation of in-house inventions in view of available literature to support patentability assessmentDrafting, filing patent application and prosecution as per the applicable laws.

We are looking for sales professional for the role of National Sales Head for our Yera Glassware business.Company profileAt YERA, we are more than just a glassware company; we are a trusted name built on decades of quality and innovation. Renowned for producing high-quality glassware since 1958, YERA is a household name in India and across the globe. Our journey started with a simple goal: to bring well-crafted, high-quality glassware into every home. Today, we continue to fulfill that mission by providing a wide range of products that combine the timeless appeal of tradition with modern design. For more info, please visit our website https://www.yera.com/yera-about-us.aspx About Role:Plan and develop sales strategies and targetsAnalysis of market and competition trendsHands on experience in building strong relationships with dealer networksCommission / incentive management Leading a sales team of RSM and ASM, their size, placements, and deciding their territories and targetsMIS -sales tracking, budgets goals vs actualsManage feedback from customersPlan and manage across country promotional Campaigns, festival offers, new opportunities Plan Institutional business ie for hotelsPerks and Reimbursement - Best In Industry.

Role & responsibilities Literature review, feasibility evaluation and study design for Bioequivalence studies Thorough understanding of national and international regulatory guidance on BioequivalenceReview of clinical study documents of Bioequivalence studies in healthy subjects and patient PK study Clinical study monitoring Knowledge of IPs management Preparation and maintenance of Trial master file Oversee the overall management of Bioequivalence studies Basic understanding of project contract with service providers Ready to take up any other relevant tasks as and when needed

Job description: Alembic Pharmaceuticals Limited is seeking a skilled Cost Accountant with expertise in MIS Reporting, Product Costing, Inventory Valuation, Cost Sheet Management, Stock Summary, Aging Report, Cost Allocation, Receivable Management, and SAP.Key Responsibilities:Prepare and present comprehensive MIS reports to support business decisions.Manage and evaluate product costing, ensuring accuracy and efficiency.Conduct inventory valuation and maintain cost sheets for effective financial planning.Prepare and analyze stock summaries and aging reports for inventory control.Oversee cost allocation processes to ensure proper financial distribution.Manage receivables, ensuring timely collections and accurate reporting.Leverage SAP for efficient financial operations and data management.Collaborate with cross-functional teams to provide financial insights and support strategic initiatives.Preferred Candidate Profile:Experience: Minimum 1 year in MIS Reporting and SAP.Qualification: Cost Accountant (ICWA/CMA) or ICWA/CMA Inter.Strong commercial acumen, analytical skills, and excellent communication abilities.Interested candidates are requested to email their updated CVs to "Vaishali.Chudasama@alembic.co.in" with the subject line "Executive/Sr. Executive (ICWA/CMA)."Be part of a dynamic team at Alembic Pharmaceuticals Limited, contributing to impactful financial operations in a leading pharmaceutical company. Take the next step in your career with Alembic Pharmaceuticals Limited !

JOB DESCRIPTIONPatient CareConduct thorough examinations of patients.Diagnose and treat medical conditions.Prescribe and administer medications, treatments, and therapies.Order, perform, and interpret diagnostic tests.Monitor patient progress and adjust treatments accordingly.To take round of all patients admitted during his/her duty to monitor medically and take history of newly admitted patients.Clinical DutiesMaintain accurate and detailed patient records.Develop and implement patient management plans.Provide pre- and post-operative care.Refer patients to specialists as necessary.Educate patients and their families on health management and disease prevention.Inform Consultant on regular basis about the progress of patient including the result of advised diagnostic test till patient gets discharged.To assist Consultants and facilitate the rounds.Getting the instructions of consultants followed and implemented. If instructions are given telephonically, note the instruction and mention instructions are take telephonically and take consultants signature when he comes.Entering the findings of investigations done on the investigation sheet.Instruct and guide the Coordinator about Pathology and Radiology test and ensure that reports are received on time.Administrative DutiesParticipate in departmental meetings and training sessions.Ensure compliance with healthcare regulations and safety standards.Collaborate with healthcare teams to plan and execute patient care programs.Supervise and mentor junior medical staff and interns.Report to Medical Administrator in case of any adverse events.Ensure Care of Patient and Medication are followed as instructed by Consultant, Infection Control Practices and Quality Assurance program of the Hospital are implemented and followed in your designated wards/areas.Emergency ResponseRespond to medical emergencies promptly.Provide immediate care and stabilization to critically ill patients.Coordinate with emergency services as necessary.Professional DevelopmentAttend the mandatory Training Programs as per hospital policies.Stay updated on medical advancements and best practices.Attend continuing education courses and professional conferences.Engage in research and contribute to medical literature if applicable.Working ConditionsHospital or clinic environment.May require evening, weekend, and on-call shifts.Exposure to infectious diseases and biohazards.Proficiency in using electronic medical records (EMR) systems.Physical RequirementsAbility to stand or sit for extended periods.Manual dexterity and physical stamina.Ability to lift and move patients as necessary.Properly groomed, in proper formals and wearing Apron.

Role & responsibilities Reporting of Unsafe Act & Unsafe conditions on daily basis.Follow the Work Permit System procedure and issue the work permit on daily requirement.To conduct and monitor the safety talk records along with HSE representative.Emergency communications as per On Site Emergency PlanEngage actively in accident and incident investigations, ensuring that corrective and preventive actions (CAPA) are promptly implement.To conduct the internal safety audits and various facility inspections and tracking the recommendation complianceTo conduct and participate in mock drills.Conduct on the job training, classroom training on Safety & Health topicsHIRA & JSA of critical activities to be conductedShould aware on the legal requirements based on various acts and rule, Maintain legal documents and ensure complianceHaving basic knowledge of chemical hazards and Material Safety Data sheet.To conduct departmental safety committee meetingsTo response emergency situation and follow On-site emergency plan.Conduct safety meeting with contract worker and supervisors.Ensure healthiness of Fire Protection and detection system.To monitor the Fire team and OHC team activities during shiftEnsure the healthy condition of fire protection and detection system

Alembic Pharmaceuticals Limited is looking for professionals in Product Manager for expanding our presence in International Pharma markets position based at Corporate Office Vadodara. Position: Product ManagerRequirements:B. Pharm + MBA or Pharma Management from a reputed instituteBetween 8 to 14 years of experience in product management or at least 1 years as a product manager in International Pharma marketingExperience in managing existing products and launching new products from Chronic Segments like Cardio Diabetic /CNS/OncoExperience in working for International markets, understanding diverse regulatory environments and market dynamics.Marketing : Ability to prepare brand plans with in-depth analysis of each market comprising competitive landscape, medical benefits , pricing and preparing a detailed marketing strategy for products with different launch strategies, communication strategy, tactics and activitiesSkills & Knowledge: Communication and Stakeholder Management: Good verbal and written communication skills to effectively collaborate with cross-functional teams, doctors, field force.Execution Skills : Regular follow up and feedback on implementationMarket Research and Analysis: Conducting in-depth market research to identify trends, competitive landscape, and unmet patient needsRegulatory Knowledge: Familiarity with international regulatory requirements (e.g., FDA, EMA)Creativity skills in developing promotional tools like VA /LBLPresentation skills: To prepare launch medical presentations for field force.Interested candidate can share Cv's on bdcv@alembic.co.in

Qualifications: M.Sc./ B.E - B.Tech (Chemical Engg.) •1 to 4 years of experience. •Experience in handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. • • Job Responsibilities:Ensure that the products are manufactured as per the cGMP.Maintain documentation as per regulatory authorities requirements like change control, and deviations.Highlight technical problems and take corrective actions. •

Alembic Pharmaceuticals Ltd. is looking for Sr. team Leader Position- Analytical Development Advanced characterization Laboratory (Peptides and Complex Generics) based at our Injectable R&D VadodaraJob Description :Lead advanced characterization activities for and peptide products and complex APIs, generics in R&D environment. Particular focus and practical experience required in developing and performing analytical methods used in the structural characterization of peptides and complexmolecules.Provides insights in area of structural characterization for complex peptide and NBCDs (e.g.purity, higher order structure derived from synthetic or natural sources) and demonstratingsameness with innovator product. Has knowledge and ability to influence regulatory authorities.Practical experience required for a range of techniques and specialist capability in one or more of these areas e.g. Determination of MW (electrophoresis, chromatographic separation), Impurity characterization (Chromatography and LCMS (HRMS) approaches), physicochemical techniques (NMR, FTIR, CD, Fluorescence Spectroscopy, DLS, AF4), Liquid chromatography techniques. Has experience of developing, running or interpreting data from these analytical approaches.Rich interpretation skills to understand and evaluate the mass spectrometry data.In depth understating of peak assignments including residue level MS/MS sequencing for establish the presence and absence of modified residue.Expertise in designing and understanding in peptide mass fragments method for match the fingerprints attributes for highly complex peptide formulations.Interested candidates may apply by sharing their resume to "msnt@alembic.co.in" with the position title "Sr. TL"

Alembic Pharmaceuticals is a leading pharmaceutical company with a strong emphasis on research and development (R&D). The Manager of Project Management in the R&D department at their Hyderabad location plays a pivotal role in overseeing and coordinating various projects to ensure they align with the company's strategic objectives.Key Responsibilities:Project Planning and Management: Define project scopes, objectives, and deliverables in collaboration with senior management and stakeholders. Develop detailed project plans, including timelines, resource allocation, and budget management. Coordinate and lead project team meetings to ensure alignment on project goals and milestones.Execution and Monitoring: Oversee day-to-day project activities, ensuring adherence to project plans and schedules. Monitor project progress, identify potential risks and issues, and implement mitigation strategies. Track project performance using appropriate systems, tools, and techniques.Stakeholder Communication: Serve as the primary point of contact for project stakeholders, including internal teams, external partners, and regulatory authorities. Prepare and present regular project updates to senior management. Foster strong relationships with stakeholders to ensure project alignment and support.Qualifications and Experience:Educational Background: A Master's degree in Pharmacy, Chemistry, or a related field is typically required. An MBA or equivalent management qualification is advantageous.Experience: A minimum of 8 to 14 years of experience in project management within the pharmaceutical industry, with a focus on R&D projects.Technical Skills: Strong understanding of pharmaceutical R&D processes, regulatory requirements, and quality standards. Proficiency in project management tools and methodologies.Soft Skills: Exceptional analytical, strategic thinking, and problem-solving abilities. Excellent communication and interpersonal skills, with the capability to influence and collaborate at all organizational levels.Interested candidates can share CV on bdcv@alembic.co.in

Alembic Pharmaceuticals Ltd is looking for Executive-Manufacturing (Pelletisation) for its formulation Unit-I based at PanelavRole & responsibilities To ensure production as per approved Batch manufacturing record. To ensure House keeping and arrangement of shop floor as per cGMP requirement. On-line documentation, review and also handle E-TMS Software .Supervision of Production activities to ensure strict follow up of SOPs & BMR.Monitor, control and checking of in process checks during processing.Work allocation and optimum utilization of Manpower and handle shop floor activity. Responsible for GMP / Training to staff and operator in all department. Execution of Qualification activies as per qualification protocol.Experienced in Audit Faced of Regulated Market ( US , WHO and EU ) Essential Job CriteriaExperience of wurster coating machine like Glatt FBE 250L,GFB 120 pro 500L,GFB 300 pro 1300L. With documentation Perks and benefits Best in IndustryInterested candidates may share their resume to prodform@alembic.co.in with Subject line "PELLET"

Alembic Pharmaceuticals is looking for Jr. Executive(Operator) - Manufacturing (Injectable) for our Formulation Unit-3, Karakhadi.Job Criteria:1-7 yearsITI/Diploma qualificationJob Responsibility:Perform assembling as per defined procedure. Operate filling machine/ Ophthalmic/ PFS machine. Operate homogenizer. Perform batch filtration activity. Perform aseptic manufacturing activity. To unload steam sterilizer and bio-decontamination chamber in co-ordination with equipment preparation and sterilization area. To take part in area qualification activity. To take part in periodic area requalification activity. Aseptic area equipment qualification, filling machine qualification, media fill process. Interested candidates may share their resumes to "injectable@alembic.co.in"

We are looking for a Network Engineer to join our Information Technology Team in Vadodara. the candidate should have a strong understanding of networking concepts and hands-on experience with Cisco, Juniper, or Palo Alto Networks along with tools like Wireshark, Nagios, and SolarWinds. Key Responsibilities: Assist in the design, configuration, and deployment of local area networks (LANs), wide area networks (WANs), and other network infrastructure components.Monitor network performance and troubleshoot issues to ensure smooth operations and minimal downtime.Document network configurations, diagrams, and procedures for maintaining an up-to-date knowledge base.Provide end-user support and resolve network-related inquiries.Preferred Qualifications:2 to 4 years of experience in network engineering or related roles.Bachelors degree in Computer Science, IT, Network Engineering, or a related field.Strong understanding of TCP/IP, VLANs, routing, and switching.Hands-on experience with Cisco, Juniper, Palo Alto Networks, etc.Familiarity with Wireshark, Nagios, SolarWinds, and other network monitoring tools.Experience in network performance optimization and tuning.Interested candidates can share th ere profile at Icv@alembic.co.in with the subject line "Executive - Network engineer "

Alembic Pharmaceuticals is looking for Technician - Instrumentation for its formulation Unit-III (General injectable) plant based at Karakhadi.Roles and Responsibilities Responsible for day to day Instrumentation maintenance/calibration activities.Good knowledge of Liquid filling machine, Lyo machine, LAF, Autoclave, Process Vessel.Strong root cause analysis skills with cGMP experience.Require exposure in maintenance and calibration of field instruments.Excellent trouble shooting skills in Automation devices/equipment to minimize loss of production time. Validation skills - commissioning, Execution of IQ/OQ. Handling of shift operation and Support over all plant engineering activities including preventive maintenance, modification plans and spare parts requirements.To participate in various activities related to project work/ modification/ qualification/Calibration and up gradation work.Ensure safe working of instrument protective devices.Interested candidates may send their resumes to engg@alembic.co.in

We are seeking a Cybersecurity professional to join our Information Technology team at Vadodara. The candidate Should have a strong understanding of information security principles, and common security technologies such as firewalls, IDS/IPS, and antivirus.Additionally, candidate should have hands-on experience with networking protocols, operating systems, and vulnerability assessment tools like Nessus, Qualys, Kali, BurpSuite, and Zap. Key Responsibilities: Assist in the implementation and maintenance of security measures to protect the organization's computer systems, networks, and data.Monitor security systems and tools for suspicious activity, unauthorized access attempts, and other security incidents.Conduct vulnerability assessments and penetration tests to identify and address security weaknesses.Analyze security logs and reports to identify trends, anomalies, and potential security threats.Participate in incident response activities, including containment, investigation, and remediation of security incidents.Assist in the development and enforcement of information security policies, standards, and procedures.Conduct security awareness training and educational programs for employees to promote a culture of security.Preferred Qualifications:Bachelor's degree in Computer Science, Information Security, Cybersecurity, or related field.Familiarity with common security frameworks and standards (e.g., NIST Cybersecurity Framework, ISO/IEC 27001, CIS Controls, OWASP).Knowledge of networking protocols, operating systems, and common security technologies (firewalls, intrusion detection/prevention systems, antivirus).Interested candidates can share there profile at "Itcv@alembic.co.in" with the subject line "Cybersecurity- Executive "

Role & responsibilities Responsible for overall operation and its compliance of Quality Control laboratory.Ensure timely testing of Water Samples, Raw/Packaging Materials, Consumable materials, In-process samples.To plan the day to day activities and follow up to be taken from supervisors for timely completion of activitiesEnsure the completion of Analytical Method Validations/ Verification /Transfer of testing methods (as applicable) used in the laboratory.Ensure availability of logistics (Standards, reagents/chemicals /solvents/columns/any other consumables) and ensure procurement of the same on time.To ensure timely completion of Analyst Qualifications for New Analysts (Either Fresher or Experienced) in the laboratory.Responsible to handle the trouble shooting of HPLC, IR, UV, Dissolution and GC instruments during the course of analysis.Initiating and implementing the GLP and cGMP activities in the departments.Handling and review of Incidents/Deviations, Out of Specifications, Out of Trends, Change Controls and CAPA as applicable.Review of trends and summary reports.To ensure that the required initial and continuing training of department personnel is carried out and adapted according to need.To ensure the calibration of instrument/equipment performed timely.To ensure and establish, validate and implement all quality control procedures.To participate in the investigation of complaints related to the quality of the product, etc.Responsible for CMC (Chemistry manufacturing and control) queries/ IR related to compliance.Handling of LIMS, DCS, Documentum, LMS & SAP software as per relevant procedures. Laboratory facility monitoring, up-gradation and to ensure up-keeping.Deliver all regulatory commitments on timeProactively identifying the issues impacting lab compliance, developing a plan and its implementation.Facing external audits Gap Analysis review and initiate the gap analysis closure by updating system SOPs/Practices and effective continuous monitoring.Participate in the Internal Audits/Self Inspection activity at site.To ensure retention and maintenance of analytical documents.To ensure timely submission of regulatory documents to respective regulatory agencies by coordination with QA and RA. Filling up all key positions and replacement of Manpower on time.Auditing of contract testing laboratories and API/Excipient vendors w.r.t. cGMP compliance.To maintain and ensure cleanliness of Quality Control laboratory and equipment’s.To impart SOP/IOCP trainings to new joinee and existing personal.

Alembic Pharmaceuticals Ltd is looking for Technician/ Operator - Manufacturing (Granulation) for its Formulation Unit-I, Panelav near Vadodara, Gujarat.Job Criteria :ITI/ Diploma/B.Sc qualification is must2-8 years of experience in Granulation Manufacturing areaJob Responsibility:Handling/Operation of sifters (Quadro ,Russell,Gansons ,Friwitt mil). Handling/Operation of Blenders. Handling/Operation of RMG , FBP ,Dry Mill,Wursters(pellets coating) Operation of various types of Granulation like top Spray, Bottom spray, tangential spray. Handling of daily verification & calibration of weighing balance. Execution of Daily Cleaning activities of area & Equipment. To ensure cGMP & HSE rules & compliances. To follow & maintain Good hygienic conditions. Handling & maintenance of Equipment /Instruments at manufacturing area Must have documentation exposure like log books, BMR entries. Exposure in regulatory approved plant. Interested Candidates may share their resume to prodform@alembic.co.in

Role & responsibilities Preparation of MIS reports on weekly, monthly and quarterly basis. Providing support to the marketing and sales team. Coordination with the field force for solving queries and data gathering. Coordination with various departments. Coordination and execution for travel arrangements such as hotel/ transport bookings, conferences and meetings. Expense Management for Field Managers.

Role & responsibilities Preparation of MIS reports on weekly, monthly and quarterly basis. Providing support to the marketing and sales team. Coordination with the field force for solving queries and data gathering. Coordination with various departments. Coordination and execution for travel arrangements such as hotel/ transport bookings, conferences and meetings. Expense Management for Field Managers.

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 shiftsJob 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)

Alembic Pharmaceuticals Limited is looking for professionals in senior business development roles for expanding our presence in European markets based at Corporate Office Vadodara.Job Description:Out Licensing:Conduct Market analysis and profiling of companies in designated countries of EU.Identify and establish contact with potential partners through regular engagement for lead generation by sharing information on product & company developments.Lead agreement negotiation till sign off & due diligence, ensure adherence to BD guidelines, contract negotiation till sign off through engaging legal and finance.Execute strategic business plan tailored to augment our footprint in the Formulation segments, in alignment with organizational objectives.External partner management:Develop and nurture robust relationships with key clients and stakeholders to fortify business alliances and cultivate enduring partnerships.Regular face to face interactions which build trust, mutual respect & bring in transparency to maximize value from existing relationshipsSales:Champion sales initiatives and surpass revenue targets.Monitor and drive Day-1 launches by actively interacting with internal CGTs & partnersEnsuing commercial life cycle management of product once launched by partnerMonitor competition, propose ideas for cost reduction etc.Other Areas::Understand regulatory requisites and industry norms governing pharmaceutical products in Europe, to navigate regulatory milieu.Provide competitive information on products under development and filling to senior management.Furnish regular reports & analysis to senior management concerning market dynamics, business performance, and actionable recommendations for refinement.To provide required inputs in new products screening process.Job Criteria: B.Pharm / M.Pharm / Any other science stream. Candidates with management degree will be given preference.10 years plus of relevant Business Development & Out-Licensing experience in require pharma EU marketShould have travelled extensively in EU and have established contacts in most of EU countries.Have demonstrated out-standing performance in execution of out-licensing deals for EU and should be well-versed with end-to-end process from lead generation to the product launch.Interested applicants can share profile at bdcv@alembic.co.in with the job title "IBU-Europe" in the subject line.

Walk-In Drive @ Vadodara for our Formulations and API sites near Vadodara, Gujarat Technical Officer/Junior Executive/Executive-Production/Packing(OSD) Email ID: prodform@alembic.co.in ProductionJob Criteria:M.Pharm/B.Pharm/Diploma/ITI. •2 to 8 years of experience. Job Role:Manage granulation, compression, coating, pelletization and capsule filling area. PackingJob Criteria:M.Pharm/B.Pharm/Diploma/ITI. •2 to 8 years of experience. Job Role: Manage bulk bottle/ blister packing, Track and Trace, serialization and documentation. •Handle machines like CVC, Servo, Countec, CAM, BQS, HONGA & UHLMANN. Executive-Quality Assurance/Quality Control Email ID: quality@alembic.co.in Quality Control (OSD)Job Criteria: M.Pharm/B.Pharm/M.Sc. • 2 to 7 years of experience. Job Role:Handle QC instruments like HPLC, LCMS, GC,UV-spectrophotometer, dissolution apparatus, KF, IPC-OES, IR spectrophotometer •Handle QMS activities and maintain lab records. Ensure QC compliances and manage GLP activities Quality Assurance (OSD/Derma)Job Criteria:M.Pharm/B.Pharm/M.Sc. •2 to 7 years of experience. Job Role:Perform area and equipment line clearance. •Perform process validation and cleaning validation. •Review BMR & BPR and manage shop floor QMS documents. •Ensure shop floor compliances and handle investigation. •Perform IPQA activity and manage the change control, deviation, Incident, OOS, CAPA etc., quality related documents of plant. Junior Executive/ Executive-Production ( API ) Email ID: apiproduction@alembic.co.in Job Criteria: M.Sc./ B.E - B.Tech (Chemical Engg.)/B.Sc. •2 to 5 years of experience. •Must have handled critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Job Role:Monitor and supervise production process to ensure compliance with SOP and cGMP. •Maintain documentation as per regulatory authorities requirement like change control, deviations. •Highlight technical problems and take corrective actions. CITY: Vadodara DATE: April 06, 2025 DAY: Sunday TIME: 9:30 AM to 3:30 PM VENUE: Alembic Pharmaceuticals Ltd.Sanskruti Hall, Alembic City, Opp. Bhailal Amin General Hospital, Alembic Road, Vadodara.

Safety Program Development and Implementation:Assist in developing and implementing safety programs, policies, and procedures.Help maintain and update safety documentation and records.Safety Inspections and Assessments:Conduct regular safety inspections and hazard assessments of facilities and equipment.Identify potential hazards and recommend corrective actions. Familiar with Risk assessment tools like HIRA, HAZOP, FMEA etc.Safety Training and Education:Conduct safety training sessions for staff, covering various safety topics.Develop and update training materials.Incident Investigation and Reporting:Investigate safety incidents and violations.Prepare reports and recommendations to prevent recurrence.Compliance:Ensure compliance with relevant safety regulations, standards, and company policies.Stay up-to-date on changes in safety regulations.Work Permit systemFamiliar with Work Permit system.Implementation of the Work permit system guideline

Alembic Pharmaceuticals Ltd. is looking for Senior Research Scientist position for its Injectable R&D plant for Vadodara Location Roles and Responsibilities : Hands on expertise in Designing & execution of product development strategies - Literature, Patent landscape, Sourcing, Pre-formulation, Prototype development, Formulation & Process OptimizationShould have experience in technology transfer of complex injectable/ peptide based products bottleneck/gap identification & trouble shootingDemonstrate expertise in drug device combination products & peptide products and their characterizationDevelop stable suspension formulations for poorly soluble drugs. Optimize formulation parameters such as particle size, viscosity, and rheological properties. Design lyophilized dosage forms for improved stability and reconstitution characteristics. Understanding of QbD applicability in Product development to ensure built in qualityConduct stability studies on various formulations according to ICH guidelines. Monitor, analyse and extrapolate the stability data to track product quality and shelf-lifeShould have sound understanding for regulatory query responseInterested Candidates can share their CV to msnt@alembic.co.in