Latest Jobs

  • Senior Officer / Asst Manager QA ( 5 - 10 yrs )

    Hyderabad
    Responsible for execution of qualification and validation activities (CQV) and other QMS integrated functions.
    Monitoring of the IQ and OQ activities and handling of the deviations if any.
    Experience in conducting quality Risk management exercises for facility layouts, utilities and equipment. 
    On hands experience in handling validation life cycle of equipments and utilities.
    Timely acquire trainings from the superior. 
    Preparation of validation master plans, performance qualification protocols and summary reports etc.
    Track the CQV schedules and escalate the impact of the validation activities.
    Prepare and review sops related to the validation activities.
    Handle and track the change controls of the project.
    Technical competencies;
    Essentials;
    Design of Biopharmaceutical facilities
    Knowledge on various Bioprocess technologies and aseptic process technologies.
    Validation life cycle.
    Quality Risk management.
    Desired;
    Design of Biopharmaceutical facilities.
    Awareness and interpretation skills of various regulatory guidelines.
    Should be currently working for a green field project or should have been worked previously.
    Qualification: M.sc, M,pharma , B.tech (Microbiology , Biotechnology, chemical Engineering.)
    Candidate should have experience in pharma (vaccines/ /injectables/ formulations background) 
    Age: 28- 32 Years

    Keyskills:QA Management, Quality, Life Cycle, Risk Management, Pharma, Formulation, QMS, CQV, IQ, OQ
  • Asst. Manager - Instrumentation & Automation ( 5 - 7 yrs )

    Hyderabad
    Should be well versed in process control in processing of liquid doses. Experience in clean utility control system and data archiving and knowledge in SCADA/PLC control system and BMS/EMS/DASS/Fire detection are necessary
    Interpreting process and manufacturing needs, review process flow diagrams, mass balances and critical parameters are required
    Ensure robustness and thoroughness in the process
    Develop URS,FRS and DDS based on the process and compliance needs and perform validation of the system and equipment
    Work with integrators to design platform architecture and review vendor designs to adhere to specification
    Must be able to interface with consultants and contractors and direct installation through external consultants and contractors.
    Ensure Project Planning/scheduling match the project needs and co-ordinate with contractors
    Must be a self-starter and energetic and function with minimal supervision.
    Collaborate with plant HSE at site with project activities ensuring all safety and environmental guidelines are adhered during construction and execution.
    Ensure that energy conservation activities are reviewed for the project and ideas implemented 
    Knowledge on Instrumentation/Automation engineering Technology for process including Formulation, Liquid Filling, Inspection, Packaging, CIP/ SIP systems.
    Experience in C&Q and validation of process automation, development of URS,FRS,DDS,SLIA is required. Experience in selection of instruments, PLC and the programming is also needed.
    5 to 7 years of experience in the field of Process Automation and Instrumentation design, selection, installation and calibration
    Qualification: Bachelor Degree in Engineering (Instrumentation/ Automation/ Electronic Engineering)

    Keyskills:
    Instrumentation, Automation, Pharma
  • Manager - Plant Operations ( 10 - 20 yrs )

    Hyderabad
    Should have experience in heading an Oral solid dosages - Formulations plant .
    Ensure smooth working at plant along with overall responsibilities of the Unit
    Improvement of GMP standards at the facility
    Maintaining & control cost of all direct/indirect material & overheads
    Experience in leading production, packaging, stores, managing material and housekeeping teams
    Formulation Products directing Production team to carry the production activities & achieve targets monitoring of routine Production operations, meeting Production targets
    Production Planning & Control Lead Purchase, Stores, Supply Chain, for the availability & release of raw & packing materials Monitoring Q.C., and Q.A. with respect to regulatory standards Carry out technical & management responsibilities
    Preparing SOP and implementing effective techniques to bring efficiency improve quality standards & achieve maximum cost saving.
    Good relations with the Govt. Agencies
    Should have good exposure towards Regulatory Audits( USFDA,TGA,MHRA, etc)
    10-20 years experience heading a pharmaceutical company plant(Formulations)
    Msc. / M. Pharm any other equivalent Qualification

    Keyskills:QC, MHRA, Production Planning Control, QA, Quality Standards, Maintenance, USFDA, TGA, Formulation, GMP
  • Asst Manager - Program Management ( 6 - 12 yrs )

    Bangalore
    Responsible for developing the project plan, business case, project schedule, project budget with the project team.
    Monitoring and managing the Projects progress against the plan and key performance
    Tracking and monitoring project milestones, developing critical 
    Applying Risk Management practices to mitigate/avoid project Risks
    Deploying Project Management methods and procedures to ensure adherence to lay down PM practices
    Managing product cost reduction process and ensure achievement of targets
    Project oriented Business case, specification, requirement, documentation, planning, scheduling, task assignment and milestone criteria development for new projects
    Coordinating with supply chain/sourcing/purchase department for prototype development and testing/certification
    Value engineering and localization process.
    Event management, customer & market study.
    Keyskills:Project Management, Project Scheduling, Program Management, Project Planning, Business Case, Schedule, Value Engineering, Tracking, Risk Management, Cost Reduction
  • Sr. Manager - Indirect Taxation ( 8 - 10 yrs )

    Hyderabad
    Managing Indirect Tax challenges including Audits, departmental queries, Show Cause Notices, appearances, appeals and litigations.
    Ensure Compliance and meets the requirements under Central Excise Laws
    Handle Service Tax, Entry Tax, Works Contract Tax and Custom Law Procedure related matters
    Ensuring proper and timely filling of Tax returns and payments.
    Optimize Cenvat / VAT Credit availment of Excise, Service tax and VAT.
    Support Business to take decision in tax efficient manner.
    Providing Supports and guidance to subordinate in the field of indirect tax.
    Partnering with other functions to ensure tax compliance in their routine transaction.
    Keep abreast of statutory amendments and circulate latest amendments to all concerns.
    Keyskills:
    Service Tax, Entry Tax, Vat, Cenvat, Central Excise, Indirect Taxation, Auditing, Tax Returns, Appeals
  • Manager/ Sr. Manager Projects - PSG ( 10 - 15 yrs )

    Hyderabad
    Complete capital projects (new projects/project expansions/ up- gradation of existing facilities) on time with quality HSE and within the approved budget.
    Developing a strong documentation package, involving from conceptual study to various phases of project like basic engineering, detail engineering, pre-commissioning / commissioning &validation of facility& equipment 
    Responsible to build a good working relation with cross functional &inter departmental teams to lead the entire project team of all disciplines.
    Responsible for the internal and external communication.
    Work load forecasting and managing work process within the team.
    Regular project review meeting within the team, with the cross functional teams and with the consultants/ vendors to control the project time to time.
    Maintain awareness on HSE requirements and implementation of the same as per the group policies, rules & regulations.
    Accurate estimation of budget for CAPEX and managing the same within the approved budget.
    Knowledge in developing and reviewing engineering designs and project execution related to facility, HVAC &utility engineering in Biopharmaceuticals
    Hands in experience in conceptual, detailed design, project planning execution and qualification of Biopharmaceutical facilities as per c GMP requirements.
    Experience other engineering disciplines like civil, electrical, instrumentation, automation &IBMS
    Candidates have knowledge on M.S Office, Auto CAD, MS Projects 
    Qualification : BE/ B.Tech Mechanical, Chemical 
    Age: 32- 37 Years

    Keyskills:
    Pre - commissioning, Project Management, Detail Engineering, Maintenance, Commissioning, Project Review, New Projects
  • Manager Purchase ( 8 - 10 yrs )

    Hyderabad
    Monitoring all purchase activities.
    Sourcing and procuring of all Formulations, Excipients and Packaging materials.
    Responsible to procure Imported Raw Materials, Packing materials. Excipients etc.
    Developing new vendors & Vendor Evaluation
    Inviting quotations, Negotiating and finalizing the pricings.
    Preparing comparison statements.
    Obtaining the necessary approvals and processing the orders in SAP.
    Obtaining all supportive regulatory documents for filling drug dossiers.
    Follow up with vendors for dispatch details.
    Follow up with Logistics team / CHA for clearance of the material.
    Initiating to obtain the necessary Licenses to import APIs.
    Preparing the raw material cost estimations for new projects.
    Managing Vendor Payments
    Aged :35-40 years
    Graduate. Having PG would be an advantage.
    08-10 years of working experience in (procure to pay)Sourcing, Procurement, Vendor Management, Strategic Planning, Cost Control and Team Management in a pharmaceutical organization dealing with formulations. 

    Keyskills:Procurement, Purchase Management, New Vendor Development, Materials, Sourcing, Dispatch, Raw Material, Import, Logistics
  • Sales Accounting Executive ( 3 - 5 yrs )

    Hyderabad

    Sales Accounting Executive


    Keyskills:Sales Accounting Executive
  • Manager Sales ( 6 - 10 yrs )

    Hyderabad
      To achieve, the primary & secondary sales target.
      Motivate the sales team.
      To monitor the market to see product is available in every retail outlet.
      To maintain sales report by day wise and weekly and monthly, salesman report and beat wise to monitor sales target and report it to General Manager.
      To maintain records of damages and claims.
      To promote the new product into the market.
      To appoint the new distributor for the market.
        Ideal candidate should have minimum 6 years of experience working with any construction chemicals company of repute and having proven track record of developing and establishing Constructions Chemicals business in any specified territory. 
        Should have good knowledge of Constructions Chemicals range of products and the applicators of the base city.

    Keyskills:Sales
  • Manager / Sr Manager - Regulatory Affairs ( 10 - 12 yrs )

    Hyderabad
    Good knowledge of regulatory pathways and options/strategy for India in particular and Europe and Rest of the World
    Knowledge and experience of preparing Common Technical Documents and Clinical Trial Application dossier
    Should prepare position papers for internal presentation to Management and Task force committee - strategy for registering the product in different markets, pros and cons, information on product related competitors in similar markets, licensing requirements and end to end understanding of regulatory procedures for registering a product in India, Europe and Rest of the world 
    Be able to manage the changes during the life cycle of the product
    Should have understanding of GMP, GDP & GLPs
    Knowledge of preparing eCTD (electronic Commercial Technical Documents)
    Main focus will be on the development and execution of regulatory strategy for the assigned components of regulatory applications and submissions
    Managing and coordinating various regulatory activities throughout the life cycle of the project/product
    Additional focus will be on appropriate planning for prioritization and coordination of activities among functional areas and within Regulatory affairs, and for timely identification and communication of project/product related concerns to the Head- RA such that same can be addressed in a timely manner
    The position is expected to organise and lead contacts with regulatory agencies and/or parent company
    Should have excellent oral and written communication skills and presentation skills
    Be able to manage small teams of 2-3 people

    Qualification: Masters in Biological Science(Immunology/ Microbiology/ Virology/ Bacteriology) or Masters in Pharmacy
    Experience: Total 10-12 yrs in pharma injectables out of which at least 7 yrs of regulatory affairs experience

    Keyskills:Regulatory Affairs, RA, Pharma, pharmaceutical, Formulation, injectables, Immunology, Microbiology, Virology, Bacteriology
  • MIS Executive ( 1 - 3 yrs )

    Hyderabad
    Should be below 26 years of age 
    Should have got 50% marks in all exams appeared 
    No academic subjects is pending for clearance (no backlogs)
    No year Gap in Education 
    Should have completed his course and is ready to join within a week ( if selected )
    Qualities - Good communication, good knowledge of the subject , Ability to work long hours, Hardworking, Proactive , Highly Disciplined, Good interpersonal skills
    Skill- Highly skilled and knowledge in Ms. Excel, should have a good knowledge in managing vast Data entry.
    B.Com/ B.A/M.A/ M.Com/ MBA(Finance) with excellent command over MS-Excel
    Graduate with high efficiency in Ms-Excel also can apply

    Keyskills:Excel, MS Excel, vlookup, Advanced Excel, MIS
  • International Business Development Manager ( 8 - 12 yrs )

    Hyderabad
    Hands of work experience in international business and operations
    Strategic and business development skills
    Sales generation activities and understanding of various business processes for sales and prescription generations
    Expertise in sales, marketing with product management exposure
    Understanding of regulatory process and experience in handling product registration assignments 
    Skills of portfolio management and balancing the product baskets across the markets 
    Coordination with in-house departments for delivery of the export orders
    Supporting internal department towards coordination with customers for handling of RA and shipment queries 
    Preparation of business budgets 
    Monitoring and generation of monthly sales analysis/ reports 
    Understanding of the distribution and financial processes 
    Export Data Analysis/Trend on competitor pricing 
    Good pharmaceutical company background
    Age: 30-35 years

    Keyskills:Marketing, Sales Analysis, International Business Development, Export, Product Management, Strategy, Business Operations, Portfolio Management, Data Analysis
  • Sr. Engineer/Engineer - Maintenance ( 5 - 8 yrs )

    Hyderabad
    To prepare/ develop/Elaborate the preventive maintenance procedure of the equipment -like Fermenters, centrifuges, autoclaves, filtration system, vial filling line, process vessel, pure steam generator, WFI& PW water systems.
    Create&manage the part numbering system for the components of Equipments
    Preparation&updating of equipment P&IDs maintaining the as built condition.
    Develop data management plan to organize all technical documents.
    Develop and maintain database of all technical documents.
    Technical competencies
    Essentials
    Experience in Bio pharmaceutical industry
    Strong Knowledge on processes equipment 
    Ability to effectively communicate verbally and in writing 
    Proficiency with Microsoft office and Auto cad.
    Desired
    Experience in preventive and breakdown maintenance in a pharmaceutical industry


    Keyskills:Preventive Maintenance, Maintenance Engineering, Database Maintenance, Technical Documentation, Data Management
  • QC Manager ( 10 - 15 yrs )

    Hyderabad
      Over all responsible for the activities of Quality Control section (RM/PM/IP/FP/ Stability & Micro) and ensure the GMP compliance in plant.
      Planning for daily analysis of in process, Finished Products, Raw Material Finished, Packaging Materials, and Stability Samples with respective intervals.
      Reviewing the Quality control analytical documents of IP (Inprocess)/FP (finished product), Stability samples, Raw material Packaging material samples of Critical care testing division (Oncology).
      Responsible for ensuring correctness of Quality control Analytical the documents as the sample testing and approvals.
      Preparation of Instrument related and General SOPs.
      Monitoring of Quality Control daily activities, Stability chamber and activities monitoring.
      Monitoring and planning of the Quality control daily activities of the oncology Division.
      Organizing and follow ups, internal audits and reviews.
      Candidate must have experience in pharma ( formulation unit,Oncology, injectables and Steroids) 


    Keyskills:QC Manager
  • QA Manager ( 10 - 15 yrs )

    Hyderabad
      Overall in charge and responsible for all operations having an impact on quality of the process and final product.
      Responsible for implementation of GMP
      Responsible for the implementation of good housekeeping and plant hygiene policy.
      Responsible for the final approval of the product for dispatch after reviewing all the quality records.(Batch manufacturing and packing records, in-process quality control records, COAs, and other related batch records like deviation/ investigation report).
      Responsible for the coordination of the cGMP and on the job training of the plant personnel.
      Responsible for the initiation, review and assessment of investigations and approval of deviation in process.
      Responsible for the approval of the standard operating procedures, standard testing procedure, General testing procedures, validation protocols, master formula records, batch records(BMR,/BPR) and all other master documents.
      Responsible for total documentation control through proper change control system
      Responsible for the validation of the process/facility /equipment.
      Responsible for the review and investigation of market complaints.
      Responsible for the coordination incase of product recalls.
      Responsible for the GMP monitoring in the plant by conduction self inspection.
      Responsible for the timely updation of the document online with the current regulatory guidelines.
      Responsible for monitoring the operations of the contract manufacturing.
      Responsible for the qualifications studies of equipment(IQ, OQ&PQ)
      Responsible for the approval of the site master File and validation master plan.
      Co- ordination with QC and marketing department for generation and approval of art work.
      Periodic assessment of the vendors through conducting vendor audit and vendor approval.
       Responsible for the assessment of non-conformance and final approval for disposition.
      To approve the external agencies carrying out the calibration and annual maintenance services.
      Responsible for training of plant personnel.
      To perform the annual product quality reviews.
      To ensure availability of adequate resources required for QA department.
      Responsible for handling of out of specification results.
      Joint responsible with Head- production and manager-QC in monitoring and control of manufacturing environment.
      Joint responsible with Head- production and manager-QC in monitoring and control of GMP compliance in plant.
      Joint responsible with Head- production and manager QC in monitoring and control of plant hygiene.
      Joint responsible with manager FRD, manager-QC assessment and conclusion of stability studies.
      Candidate must have experience in pharma ( formulation unit,Oncology, injectables and Steroids) 


    Keyskills:QA Manager
  • Sr Manager Purchase ( 10 - 15 yrs )

    Bangalore
    10-15 years of working experience in Sourcing, Procurement, Vendor Management, Strategic Planning, Cost Control and Team Management in a pharmaceutical organization dealing with formulations.
    Monitoring all purchase activities.
    Sourcing and procuring of all APIs, Excipients and Packaging materials.
    Responsible to procure all Imported Raw Materials, Packing materials for all plants.
    Developing new vendors & Vendor Evaluation
    Inviting quotations, Negotiating and finalizing the pricings.
    Preparing comparison statements.
    Obtaining the necessary approvals and processing the orders in SAP.
    Obtaining all supportive regulatory documents for filling drug dossiers.
    Follow up with vendors for dispatch details.
    Follow up with Logistics team / CHA for clearance of the material.
    Initiating to obtain the necessary Licenses to import APIs.
    Preparing the raw material cost estimations for new projects.
    Managing Vendor Payments
    Keyskills:Procurement, Purchase Management, New Vendor Development, Materials, Sourcing, Dispatch, Raw Material, Import, Logistics
  • AGM / DGM - QA ( 10 - 15 yrs )

    Bangalore
    Third party audits, International and domestic Vendor audit (Packaging materials, Excipients, LL, P2P and APIs) vendor qualification.
    Knowledge of Documentation activities for cGMP and Regulatory compliance.
    Have effective communication skill and willing to share information and contribute my best efforts to ensure the achievement of team objectives.
    Conducting audit of manufacturing plants and Vendors supplying excipients and packing materials.
    Planning, Preparing, Conducting and Reporting of GMP/Quality audits.
    Writing Audit Reports.
    Evaluation of audit result for the audits done.
    Maintenance of audit data in a related data system.
    Participation in internal and regulatory audits as required.
    Preparation and exercising the sent and received Quality agreements.
    Knowledge of General QA/QC documentation, QC Specifications, raw materials & Finished Product Stability documents.
    Knowledge of reviewing Dossiers for the components being used for regulatory, CIS and emerging markets and always have interest to have information in coordination with RA dept.
    Good understanding and review on BMRs, BPRs, process validation data for regulatory, CIS and emerging markets.
    Writing/revision of SOPs as and when required.
    Process Validation as per validation protocols.
    Keyskills:QA, Pharma, Vendor audit, Quality Assurance
  • Lecturer Commerce / Management ( 5 - 8 yrs )

    Hyderabad
      Looking for Lecturers with experience to teach Curriculum courses (Commerce/Management) of BBA,B.Com (comp), B.Com (Gen) and B.Com (Foreign Trade) Programs of Osmania University. Candidates who have experience can apply for Full/part time positions. 
      Salary will not be a constraint for the right candidate.
      Should have got 50% marks in all exams appeared 
      Qualifications: M.Com/MBA (First Class)from a recognised University. UGC-NET/Ph.D is desirable.
      Experience: Minimum 5 years in Teaching UG courses.
      Marketing, Accounting, General Management & Statistics - Vacancy

    Keyskills:
      Lecturer
  • Vice President - Operations ( 20 - Above 20 yrs )

    Bangalore
    Conceptualizing, planning and executing the retail operations, ensuring sales growth and driving initiatives which are in line with organization business goals.
    Strategic level experience in identifying, designing and implementing effective plans to expand the potential market
    Scaling up operations and business initiatives for revenue gains and achieving profitability 
    Champion Business process improvement initiatives 
    Independently responsible for Profit & Loss as SBU Head.
    Handle Business plans, operations and assess revenue potentials.
    Overall should have a strong exposure in Business development, Strategic Planning, Operations Management, Brand Management & Marketing activities, Training & Development of the Team. 
    Effective leadership and communicative style, relationship building, strong analytical and problem solving abilities. 
    Qualification & Experience: Post Graduate in Business Management from reputed Institutes with around 20 years of experience with Leading Retail Companies, preferably Pharmaceuticals, having handled the business independently.


    Keyskills:
    Vice President, VP, Business development, Operations Management, Brand Management
  • Asst Manager QC ( 5 - 10 yrs )

    Visakhapatnam
    Responsible for Sampling and Analysis of Raw materials for solubility, LOD, Sulphated ash, water content, Identification by IR / UV , Specific optical rotation, Assay by HPLC or Auto titrator, Related substances by HPLC, 
    Residual solvents by GC
    Responsible for Analysis of Finished products for Average weight, Friability, DT, Hardness, Dissolution, Uniformity of dosage units by 
    Content uniformity, Assay , RS as per Spec & STP
    Qualification of In-house working standards against USP , EP Reference standards
    Responsible for Calibration of HPLC, GC, Dissolution apparatus, FTIR, UV-Visible spectrophotometer, KF autotitrator, Potentio meter, 
    Polarimeter, M.R.Apparatus, Tapped density apparatus, Analytical balances.
    Analytical data review for all Raw materials, packing materials, In-process and Finished products
    Initiation and closing of Change control, Lab Incidents, OOS, and Deviations.
    Preparation and review of standard operating procedures
    Preparation and review of Spec & STPs
    Timely reporting the quality issues and status to Manager-QC
    Instruments Handled:
    Please Note: CV from API Experience only will be considered.
    Keyskills:Uv, Hplc, Kf, Autotitrator, Polarimeter, Gc, Dissolution Apparatus, Finished Products, Qc
  • Marketing Executive ( 5 - 5 yrs )

    Hyderabad
    Developing new customer base and expanding business with potential partners.
    Should focus on business development efforts and new product registrations and to increase existing sales.
    Responsible for converting inquiries into orders. Preparing quotation, PI and negotiation with customers.
    Should interact with agents/customers to understand the regulatory requirements for registration of new products in their country.
    Responsible for Commercial and Legal negotiations and closure of agreements for the same with customers, International partners and suppliers.
    Responsible for Timely processing and delivery of the export orders.
    Responsible for Export Data Analysis. & preparing various MIS Reports.
    Strategic Partnering: Finding International partners for co-development, Marketing and distribution.
    To generate growth through attracting in-licensing opportunities.
    Should Analyze Competitors Brand performance, Growth and Market share in the respective country.
    Qualification : Any Graduate / Post Graduate ( Must be from Pharma Industry only)

    Keyskills:Sales, Marketing, Business Development, Distribution, Strategy, Negotiation, New Product, Mis Reporting, Data Analysis
  • Site Accountant - Gujarat ( 6 - 8 yrs )

    Gujarat
    Managing day to day Accounting operations and payments.
    Maintaining Bank Book and Cash Book.
    Preparing any type of Vouchers and Invoices.
    Preparing Employees Attendance and Payroll
    Preparation of Cash Book, Ledger Posting, and BRS.
    Timely payment of TDS, CST, VAT payables, receivables and return filing.
    Verified Invoices submitted for payment request
    Maintaining Computerized Accounts data entry 
    Preparation of Cash Budget, Expenditure and Due statements.
    Preparing Stores related Log Books.
    Related to Accounts, Stores and Departments in the prescribed format. 
    Good working use of computer. Ms word/ excel / ERP software. 
    Experience : 6 years and above ( in Mechanical construction) 

    Keyskills:Accountanat, ERP, B.COM, M.COM
  • Manager- Automation/ Instrumentation ( 8 - 13 yrs )

    Hyderabad
    Manager is required to lead the maintenance activity related to instrumentation/automation of process equipment & utility dedicatedly. 
    Responsible to guide the team of engineers & technicians involved in maintenance of equipment / Utility related to instrumentation & Calibration.
    Responsible to prepare & implement strategies for smooth running of process equipment & long term sustainability of performance of equipment.
    To minimize breakdown of equipment/systems and increasing the availability of equipment for continuous operation.
    Responsible for monitoring of day to day operations / activities, trouble shooting and documentation.
    Responsible for qualifications pf PC/PLC based systems. Execution of modernization projects.
    Responsible for design & implementation of preventive maintenance plan & other scheduled/non-scheduled tasks.
    Preparation of budget, management of spare part, cost control.
    Responsible to achieve the objectives related to maintenance & reports preparation.
    Essentials:
    Automation/ Instrumentation (rich experience in handling automation part of process equipment like vial filling machine, autoclave, dry heat sterilizer, fermented, SIP/CIP, pressure vessels, LAFU, labelling machines and utility systems).
    Desired:
    Knowledge HVAC/Water System & Autocad-moderate competency.
    Age:  32-40 Years
    Qualification: Diploma/ BE/ B.Tech Instrumentation, Industrial Automation
    Candidate should have experience in pharma industry

    Keyskills:Plc, Design, Water System, Fire Protection, Preventive Maintenance, Autocad, Building Management System, Instrument Calibration, Process Equipment, Fire Alarm System
  • Manager - Process Equipment ( 8 - 12 yrs )

    Hyderabad
    Maintenance manager is required to lead the maintenance activity related to process equipment of FFP & Bulk suite dedicatedly. 
    Responsible to guide the team of engineers & technicians involved in maintenance of process equipment (FFP & Bulk).
    Responsible to prepare & implement strategies for smooth running of process equipment & long term sustainability of performance of equipment.
    Responsible to minimize breakdown of equipment/systems and increasing the availability of equipment for continuous operation.
    Responsible for monitoring of day to day operations / activities, trouble shooting and documentation.
    Responsible for equipment qualifications/documentation & execution of modernization projects.
    Responsible for design & implementation of preventive maintenance plan & other scheduled/non-scheduled tasks.
    Preparation of budget, management of spare part, cost control.
    Responsible to achieve the objectives related to maintenance & reports preparation.
    Essentials:
    Maintenance of FFP machines- vial filling machines, capping machines, fomenters, vial washing & sealing machines, sterilizers and Purified water systems, WFI systems.
    Desired:
    Knowledge HVAC/ Water System & Autocad-moderate competency.
    Age: 32 - 40 Years
    Qualification: Diploma/ B/B.Tech Mechanical

    Keyskills:Design, Water System, Process Equipment, Pressure Vessels, Preventive Maintenance, Budget Management, Cost Control
  • HR Officer ( 1 - 3 yrs )

    Hyderabad
    Responsible for handling end-to-end HR activities 
    Should be below 26 years of age 
    Should have got 50% marks in all exams appeared 
    No academic subjects is pending for clearance (no backlogs)
    No year Gap in Education 
    Should have completed his course and is ready to join within a week ( if selected )
    Qualities - Good communication, good knowledge of the subject , Ability to work long hours, Hardworking, Proactive , Highly Disciplined, Good interpersonal skills
    Skill- Highly skilled and knowledge in Ms. Excel, should have a good knowledge in managing vast Data entry.
    B.Com/ B.A/M.A/BBA(HR)/MBA(HR) with excellent command over MS-Excel
    non MBA with high efficiency in Ms-Excel also can apply

    Keyskills:HR, Excel, MS Excel, IR, Macro, vlookup, statutory

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