23460 Verification Jobs - Page 18

 Maintain GLP in the laboratory as per regulatory requirement.  Analytical method development as per ICH Guidelines.  To perform In-process, routine and stability sample analysis.  Perform the analytical method verification / validation as per protocol.  Analytical method transfer to QC Laboratory.  Documentation as per the GLP requirement.  Trouble shooting during day to day analysis with proper instrument care.  Perform dissolution development, multimedia dissolution and CDP activity.  Working standard preparation as per SOP.

Management of stores activities for Raw materials. Receipt of Raw materials. To ensure Quality and cGMP compliance of the products being manufactured. Responsibilities: Receipt of Raw Material for main Pharma stores. To check the environmental parameters like Temperature, RH, pressure difference etc. Daily verification of weighing balance and daily documentation. Reconciliation of materials. Stock verification with internal and external auditors. Maintain of Rack location in SAP as per physical. Dispatch of material to Loan license and Ethiopia plant. Handling of retest, rejected, expired materials. Compliance to cGMP with respect to regulatory standards. Maintaining the proper housekeeping in Stores area. Training attends as per schedule. Material loading/loading of Rifampicin at Rifampicin mfg./store area.

Perform Analytical Method validation and verification as per the protocol. Documentation as per GLP requirement. Proper archival of validation books and reports. Troubleshooting during day-to-day analysis with proper instrument care. Response to regulatory and customer queries.

 Maintain GLP in the laboratory as per regulatory requirement.  Analytical method development as per ICH Guidelines.  To perform In-process, routine and stability sample analysis.  Perform the analytical method verification / validation as per protocol.  Analytical method transfer to QC Laboratory.  Documentation as per the GLP requirement.  Trouble shooting during day to day analysis with proper instrument care.  Perform dissolution development, multimedia dissolution and CDP activity.  Working standard preparation as per SOP.

Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. To follow safety Procedure in Microbiology laboratory (Main Pharma-QC) To attend the training as per schedule. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Preparation and sterilization of media for analysis. Used media destruction as per respective SOP. Responsible for cleaning & monitoring of laboratory. Responsible for online documentation. Sampling and Microbiological/ chemical testing of Purified water, Water for injection, Potable water samples and pure steam condensate samples. Plate / Tube verification and release and on-line data recording Work allocation and distribution To ensure the training about the changes in standard operating procedures (SOP), if required. Review of analytical data Change control, master document preparation and review Regulatory Audits and Periodic self-inspection Do any other Work assign by HOD.

" Ensure the cGMP Compliance and schedule M compliance in production. Ensure the completion of production targets with zero quality issue. Ensure the timely completion of investigation and implementation of corrective and preventive action. Ensure the development progress periodically of personals and take necessary corrective action. Ensure the compliance of inspection /Audit in coating area and revision of procedures/SOPs To follow daily plan prepared based on the monthly/weekly plan. To ensure the availability of core tablets, coating materials and equipment before plan. To distribute the operational activities among the supervisors and operators of coating, capsule, printing and inspection to complete the daily targets. To set & achieve the daily targets to achieve monthly targets. Trace the daily output of equipment with respect to the daily target and intimate the deviation with justification in OEE report. To co-ordinate with cross functional departments (i.e. Dispensing, Granulation, Compression) for input material and co-ordinate with WIP, packing, QA, QC for sampling and release to packing. To ensure the SAP transactions of completed products. To ensure the cleanliness of area & equipment and to ensure the equipment parts, change parts are place at designated location with proper status labelling. Ensure the procedures are followed as per Standard operating procedure and continuous improvement in system/documents. To verify the executed documents (BMRs) on daily basis and SOP formats on daily basis or Monthly basis based on the frequency of review. To ensure all the SOPs are available at working place for ready reference. To maintain the SOP records (i.e. Silicon tube, sieves, Audit trial review, consumable materials, etc.) for ready reference. To maintain the records of equipment and instruments for calibration/verification and co-ordinate with cross functional team for timely calibration/verification where required. To ensure the calibration tags/verification tags available with equipment or instruments and to maintain the calibration, verification certificate for ready reference. To provide the equipment are working as per design. To verify the need of predictive maintenance and building maintenance and intimate to maintenance team through BDIS. To ensure and tracking of the Users for each equipment/system for all supervisors and Operators in active status. To ensure the no wastage of utilities when not required. Any other job described by department/production/unit head."

 Maintain GLP in the laboratory as per regulatory requirement.  Analytical method development as per ICH Guidelines.  To perform In-process, routine and stability sample analysis.  Perform the analytical method verification / validation as per protocol.  Analytical method transfer to QC Laboratory.  Documentation as per the GLP requirement.  Trouble shooting during day to day analysis with proper instrument care.  Perform dissolution development, multimedia dissolution and CDP activity.  Working standard preparation as per SOP.

 Maintain GLP in the laboratory as per regulatory requirement.  Analytical method development as per ICH Guidelines.  To perform In-process, routine and stability sample analysis.  Perform the analytical method verification / validation as per protocol.  Analytical method transfer to QC Laboratory.  Documentation as per the GLP requirement.  Trouble shooting during day to day analysis with proper instrument care.  Perform dissolution development, multimedia dissolution and CDP activity.  Working standard preparation as per SOP.

" Follow cGMP and GLP practices in Quality Control Lab. To perform the qualification of working standard. To Maintain Inventory management for all chemicals, solvents and laboratory required items. To follow safety Procedure in QC department. Maintain all the chemicals opening date and expiry date Responsible for procurement of chemicals, glassware, stationary, impurity, reference standard, column, consumable etc. To prepare SOP and manage the documents. To investigate incidence, OOC and take appropriate CAPA. To perform the calibration, verification and maintenance of instruments. To ensure compliance related GLP-activity in QC. Participate to complete the training for new comers as well as refresher training. To ensure and maintain the HPLC / GC column. To ensure and maintain the all applicable SST solutions as per SOP. To maintain the documents of OOS, OOT, Analyst qualification, Calibration etc. To maintain the ROA (Stability, RM and FP) To perform the qualification of working standard To prepare volumetric solution and bench reagent. To maintain Reference standard, working standard and Party standard. To reviewed preventive maintenance done by service engineer of instruments and equipment. To maintain and ensure the availability of chemical, glassware, stationary, column consumable etc. for smooth operation of QC testing. To maintain all primary standards. To maintain laboratory safety To maintain Laboratory First aid Box To maintain Preventive maintenance of Laboratory equipment’s. To maintain AMC & CMC for all critical equipment’s in the Laboratory. To Preparation and Maintenance of all Working /Reference standards and Reference standard stock solutions and its consumption records. To monitor Refrigerator/Freezer temperature mapping daily. To Destruction of expired Chemicals /Solvents in the laboratory and its records. To ensure the cleanliness of the laboratory. To do any other Work assign by HOD."

To prepare and review the PQRs. To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. To verify & review of Ingredient manufacture name (Vendor Name) & TSE-BSE certificate for PQR Compilation. Review for Qualification & validation data for compilation of PQR. To perform continuous process verification of the product. To initiate & review Change Control in LIMS, Deviation & CAPA in EPIQ. Any other job assigned time to time by HOD as per requirement.

Verify Receipt of Raw Material & Packaging Material for stores. Verify SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. Verify the environmental parameters like Temperature, RH, pressure difference etc. Verify Daily verification of weighing balance and daily documentation. Verify Reconciliation of materials. Stock verification with internal and external auditors. Verify to Maintain of Rack location in SAP as per physical. Verify Preparation of packing list and keep ready the material for Ethiopia. Verify timely dispatch of material to Loan license and Ethiopia plant. Verify handling of retest, rejected, expired materials. Co-ordinate with quality control / production / maintenance /QA / SCM/ Purchase / Contract Mfg etc. departments. For smooth functioning of stores activities. Compliance to cGMP with respect to regulatory standards. Maintaining & verify the proper housekeeping in Stores area. Training attends as per schedule. Revise or change the Store SOP for comply to any Audit/ for as per time schedule. Ensure receipt and on-line documentation of the materials received as per SOP. Ensure all the operating systems are maintained as per the SOP. To receive the materials as per the amended approved vendor list. Ensure no loss of production due to non-availability of dispensed materials. Ensure clearance of obsolete, rejected and Artwork change materials on timely basis with coordination with Planner. Ensure to carry out GMP self-inspection within the department once in a month and compliance on the observed deviations. Ensure no major observation during internal as well as external audits Ensure 100% compliance to the existing and no unplanned deviation on the shop floor To review and correct gaps between SOP and policies and implement the audit (internal & external) findings.

Follow cGMP and GLP practices in Quality Control Lab. To perform the qualification of working standard. To Maintain Inventory management for all chemicals, solvents and laboratory required items. To follow safety Procedure in QC department. Maintain all the chemicals opening date and expiry date Responsible for procurement of chemicals, glassware, stationary, impurity, reference standard, column, consumable etc. To prepare SOP and manage the documents. To investigate incidence, OOC and take appropriate CAPA. To perform the calibration, verification and maintenance of instruments. To ensure compliance related GLP-activity in QC. Participate to complete the training for new comers as well as refresher training. To ensure and maintain the HPLC / GC column. To ensure and maintain the all applicable SST solutions as per SOP. To maintain the documents of OOS, OOT, Analyst qualification, Calibration etc. To maintain the ROA (Stability, RM and FP) To perform the qualification of working standard To prepare volumetric solution and bench reagent. To maintain Reference standard, working standard and Party standard. To reviewed preventive maintenance done by service engineer of instruments and equipment. To maintain and ensure the availability of chemical, glassware, stationary, column consumable etc. for smooth operation of QC testing. To maintain all primary standards. To maintain laboratory safety To maintain Laboratory First aid Box To maintain Preventive maintenance of Laboratory equipment’s. To maintain AMC & CMC for all critical equipment’s in the Laboratory. To Preparation and Maintenance of all Working /Reference standards and Reference standard stock solutions and its consumption records. To monitor Refrigerator/Freezer temperature mapping daily. To Destruction of expired Chemicals /Solvents in the laboratory and its records. To ensure the cleanliness of the laboratory. To do any other Work assign by HOD.

Major Purpose Of The Job Analytical Method Development by HPLC for all Project. Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. Calibration of HPLC system. To maintain GLP in working environment. Regularly co-ordination with project scientist. Preparation of analytical data and submit for review. Principal Tasks And Responsibilities Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. Developed New HPLC Method for all stages of new molecule as well as modified old method as per regulatory requirement. HPLC Method verification of new developed method. Calibration of HPLC’s as per SOP and maintenance of HPLC Systems. Trouble shooting during day to day analysis and discuss with R&D people of respective project. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports.

" Receipt of Raw Material for main Pharma stores. SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. To check the environmental parameters like Temperature, RH, pressure difference etc. Daily verification of weighing balance and daily documentation. Reconciliation of materials. Stock verification with internal and external auditors. Maintain of Rack location in SAP as per physical. Preparation of packing list and keep ready the material for Ethiopia. Dispatch of material to Loan license and Ethiopia plant. Handling of retest, rejected, expired materials. Co-ordinate with quality control / production / maintenance /QA / SCM/ Purchase / Contract Mfg etc.depts. For smooth functioning of stores activities. Compliance to cGMP with respect to regulatory standards. Maintaining the proper housekeeping in Stores area. Training attends as per schedule. Revise or change the Store SOP for comply to any Audit/ for as per time schedule. Material loading/loading of Rifampicin at Rifampicin mfg./store area. As and when required goes to Cephalosporin & Penicillin area for un loading and loading Material."

This role would be part of Analytical Research & Development for Formulations Research team. The key responsbilities would be as mentioned below: Analytical methods validation and report preparation on LCMS (for Nitrosamine impurities, NDSRI impurities etc.) Analytical Method development and report preparation on LCMS (for Nitrosamine impurities, NDSRI impurities etc.) Routine and stability sample analysis Analytical method verification of drug products and drug substances on LCMS Key Skills Required Analytical method development by LCMS & validation Trouble shooting of Instruments Impurity maintenance

Ensure the cGMP Compliance and schedule M compliance in production. Ensure the completion of production targets with zero quality issue. Ensure the timely completion of investigation and implementation of corrective and preventive action. Ensure the development progress periodically of personals and take necessary corrective action. Ensure the compliance of inspection /Audit in coating area and revision of procedures/SOPs To follow daily plan prepared based on the monthly/weekly plan. To ensure the availability of core tablets, coating materials and equipment before plan. To distribute the operational activities among the supervisors and operators of coating, capsule, printing and inspection to complete the daily targets. To set & achieve the daily targets to achieve monthly targets. Trace the daily output of equipment with respect to the daily target and intimate the deviation with justification in OEE report. To co-ordinate with cross functional departments (i.e. Dispensing, Granulation, Compression) for input material and co-ordinate with WIP, packing, QA, QC for sampling and release to packing. To ensure the SAP transactions of completed products. To ensure the cleanliness of area & equipment and to ensure the equipment parts, change parts are place at designated location with proper status labelling. Ensure the procedures are followed as per Standard operating procedure and continuous improvement in system/documents. To verify the executed documents (BMRs) on daily basis and SOP formats on daily basis or Monthly basis based on the frequency of review. To ensure all the SOPs are available at working place for ready reference. To maintain the SOP records (i.e. Silicon tube, sieves, Audit trial review, consumable materials, etc.) for ready reference. To maintain the records of equipment and instruments for calibration/verification and co-ordinate with cross functional team for timely calibration/verification where required. To ensure the calibration tags/verification tags available with equipment or instruments and to maintain the calibration, verification certificate for ready reference. To provide the equipment are working as per design.

Method verification of new HPLC method for all stages of new molecule as well as modified old molecule method as per regulatory guidelines. Calibration and maintenance of HPLC systems as per SOP. Maintaining records for all analytical reports by entering all the data in raw note book and timely release of analytical report. To maintain analytical data and report.

To assure Quality and cGMP compliance of the products being manufactured and Packed for Liquid Manufacturing Block. To give Area /Equipment clearance i.e. checking and approval of all manufacturing & filling. To verify environmental condition i.e. Temperature, Relative Humidity & Pressure Differential condition in all for said areas are within acceptable range at all the time during operation throughout the shift. To ensure daily verification of weighing balance with standard weights. To perform filled volume & weight method and leak test as per MMD-I & SOP. To perform sampling of bulk and finished product for each batch at the end of the batch as per SOP entry into sampling log and submit the samples to QC for analysis. Record review, To review the Batch Manufacturing Records for on line entries at each stage. To review sequential log of machines. To review environmental condition records. To review of area cleaning logs. To release the batches for further processing. To review and checking Batch Manufacturing Records for reconciliation, correct entries, completeness, affixing of release status labels. Reporting to shift in charge to address the observations under Deviations, unusual observation Daily report of total activities performed Liquid Packing To give line clearance i.e. checks and approval of all packing. To perform checking and approval of overprinting details on printed packing material like blisters, cartons, labels etc. As per Batch Packing record. To verify the correctness of primary and secondary packing materials of product being packed as per CMOF and MMD-II. To perform periodic checks of overprinting details, number of units per pack, absence of empty pocket etc. To perform spot-checking on inspected bottles SOP. Record review, To review the Batch Packing Records for on line entries at packing stage. To review sequential log of machines. To review of area cleaning logs. To co-ordinate with packing supervisor in relation to the issue related to packing. Any job assigned time to time.

Major Purpose Of The Job Negotiation with vendor for lowest price. New vendor development for alternate source. SAP operation. Market information. Resolving day to day issues with internal and external customers. Team work. Cross functional meeting with internal customers for update and issue resolution. Follow up with vendors for delivery / quotation and if any requirement for our internal customers Ensure timely delivery of primary & secondary packaging materials for each location Ensure timely vendor payments Principal Tasks And Responsibilities Negotiation Ensure Quotations from different vendors are arranged as per SOP Verification of Comparative Analysis and negotiation Finalize the price considering budget, required quantity and delivery on time considering lead time. Vendor Development, to have an alternate source Advise team to select the items for alternate vendor i.e. for additional source/quality improvement/price etc. as an when required Primary selection of vendor for new development by team. Discussion with new vendor for their capabilities, plants, terms etc. Ensure approvals of QA, QC, Plants for submitted Sample Vendor audit if required & negotiations Arrange commercial lot Market Information Contacts with vendor for new development Newsletters, internet etc. Visit to the vendor premises for latest update Visit to concern trade fare/seminar etc.

Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. To follow safety Procedure in Microbiology laboratory (Main Pharma-QC) To attend the training as per schedule. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Preparation and sterilization of media for analysis. Used media destruction as per respective SOP. Responsible for cleaning & monitoring of laboratory. Responsible for online documentation. Sampling and Microbiological/ chemical testing of Purified water, Water for injection, Potable water samples and pure steam condensate samples. Plate / Tube verification and release and on-line data recording Work allocation and distribution To ensure the training about the changes in standard operating procedures (SOP), if required. Review of analytical data Change control, master document preparation and review Regulatory Audits and Periodic self-inspection Do any other Work assign by HOD."

Entity: Production & Operations Job Family Group: Engineering Group Job Description: bp Technical Solutions India (TSI) center in Pune, strives to build on bp’s existing engineering and technical strengths to deliver high quality services to its hydrocarbons and new energy businesses worldwide. TSI brings together diverse engineering capability to provide technical services across a range of areas including engineering, maintenance, optimization, data processes, projects and subsurface, to deliver safe, affordable and lower emission energy, while continuously innovating how we work. At bp, we’re reimagining energy for people and our planet. We’re leading the way in reducing carbon emissions and developing more balanced methods for solving the energy challenge. We’re a team with multi-layered strengths of engineers, scientists, traders and business professionals determined to find answers to problems. And we know we can’t do it alone. We’re looking for people who share our passion for reinvention, to bring fresh opinions, ambition, and to challenge our thinking in our goal to achieve net zero! Let Me Tell You About The Role Role Synopsis: The Site Projects Engineering Manager - TSI will join the site projects organization to oversee and lead the bpTSI-based discipline engineering team. They and their team will need to provide engineering expertise, oversight, judgment and support to projects across all the site projects locations. This will include guiding the engineers as they oversee the design, verification and interfaces with the engineering design contactor, project management and procurement. The role is Pune-based but might require some contractor-facing work at major engineering contractor office locations in India What You Will Deliver Provide centralized engineering leadership for the discipline engineers supporting the P&O bp Solutions Site Projects. Balance demand and workload for engineers who support more than one location Interface with the bpS Discipline Leads based in TSI on engineer performance Interface with all of the Site Projects EMs at their respective locations Actively support recruiting of discipline engineers for the team Ensure there is cross-discipline consistency across all site projects being supported by the TSI-based engineers Coach discipline engineers on the projects engineering guide and PDCP Responsible as Site Projects Engineering Manager for the Terminals and Pipelines (T&P) projects. Responsible for driving engineering quality and addressing engineering quality related issues. This includes identifying non-conformances and resolving actions. Conduct engineering self-verification, oversight and audit activities of both BP and engineering contractors. As needed, support performance management of both bp and engineering contractors through implementation, measurement, and analysis of relevant KPI’s to drive continuous improvement Support the Site Projects Team and Engineering Contractor(s) to deliver engineering scopes in front-end loading stages (FEL) and Detailed Engineering of projects, including to: Coach discipline engineers on ways of working within bp’s project processes Interface with S&OR on deviations (as requested) work with engineering contractor(s) to verify they are performing required activities in line with project schedules, and assist bp’s Site Projects Engineering Managers in contract performance management Ensure that engineering contractor(s) apply bp’s Engineering Practices in engineering designs determine risks to project delivery and ensure adequate risk mitigation plans are in place provide expertise to project MoCs (as needed) Responsible for engineering risk management for T&P projects. Drive decisions by balancing business drivers with design alternatives What You Will Need To Be Successful Must have educational qualifications: Bachelor’s or Master’s Degree in relevant Engineering subject (including Chemical, Process, Electrical, Mechanical) Preferred education/certifications: Chartered Engineer or registered professional engineer Minimum years of relevant experience: 15+ years in oil and gas/petrochemical/ refining/ chemical or equivalent, with minimum five (5) years’ experience of Engineering work in Capital projects. Strong preference will be given to experience in brownfield projects. Total years of experience : 15+ Years Must have experiences/skills: Required experience and working knowledge of the following: Management of a team of engineers Risk management processes, including being able to guide others through a risk-based decision process Process safety processes, including Design Hazard Management, Management of Change and Inherently Safer Design. General understanding of the project stages including what is accomplished in each Management of engineering design contractors Engineering specifications, including international industry codes & standards. Requirements of the procurement process Strong technical knowledge and experience with engineering, maintenance and operation of equipment and/or systems. This can include troubleshooting support, reliability, obsolescence and equipment lifecycle issues in oil & gas processing facilities Detailed understanding of FEL-3 and Detailed Engineering on projects Ability to communicate effectively with all levels of the project team, contractors and project leadership. Track record of improving safety and reliability at an industrial facility, preferably oil/gas/petrochemical processing through engagement and influence Developing and building networks and respects the contribution of others. Demonstrated ability to manage multiple priorities and possesses good organization, facilitation and group coordination skills Good to have experiences/skills: Experience in an operational environment, brownfield modifications, front end engineering, scoping, technical evaluation Experience of working with remote team and collaborative approach to delivery Proven track record in cross-functional engineering improvements Consistently delivers results under pressure You will work with bp Solutions Site Projects Teams Site Projects Engineering Managers Engineering Discipline Lead – Site Projects Engineering Contractor(s) bp Discipline Engineers Operations personnel Refinery and Production Teams Shift Working hours (2 – 11 pm) to interface with all teams % travel requirements 10% At bp, we provide the following environment & benefits to you: Life & health insurance, medical care package Flexible working schedule: home office up to 2 days / week, based on team agreement Opportunity to build up a long-term career path and develop your skills with a wide range of learning options Family friendly workplace e.g.: parental leave, Mother-baby room Employees’ wellbeing programs e.g.: Employee Assistance Program, Company Recognition Program Possibility to join our social communities and networks Assets like phone and company laptop are provided from the first day of employment with other equipment if requested Why Join our team? At bp, we support our people to learn and grow in a diverse and challenging environment. We believe that our team is strengthened by diversity. We are committed to crafting an inclusive environment in which everyone is respected and treated fairly. Diversity Statement: At bp, we provide an excellent environment and benefits such as an open and inclusive culture, a great work-life balance, tremendous learning and development opportunities to craft your career path, life and health insurance, medical care package and many others! Diversity sits at the heart of our company and as an equal opportunity employer, we stay true to our mission by ensuring that our place can be anyone's place. We do not discriminate based on race, religion, colour, national origin, gender and gender identity, sexual orientation, age, marital status, veteran status or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application and interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Travel Requirement Up to 10% travel should be expected with this role Relocation Assistance: This role is eligible for relocation within country Remote Type: This position is not available for remote working Skills: Anomaly assessment and management, Defect Elimination, Equipment criticality assessment, Equipment maintenance and inspection strategies, FAT and commissioning, Fatigue Analysis, Fitness for Service, Flanged joint, Integrity Management, Mechanical seals and support systems, Monitoring and data interpretation, Piping, hoses and tubing, Piping vibration, Pressure systems regulatory requirements, Pressure Vessels, Selection and design of pipeline equipment, Stress analysis for integrity and leakage, Valves used for isolation, Wind Turbines Legal Disclaimer: We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, socioeconomic status, neurodiversity/neurocognitive functioning, veteran status or disability status. Individuals with an accessibility need may request an adjustment/accommodation related to bp’s recruiting process (e.g., accessing the job application, completing required assessments, participating in telephone screenings or interviews, etc.). If you would like to request an adjustment/accommodation related to the recruitment process, please contact us. If you are selected for a position and depending upon your role, your employment may be contingent upon adherence to local policy. This may include pre-placement drug screening, medical review of physical fitness for the role, and background checks.

Position : Assistant Manager Location : Mumbai Reporting To Manager - Accounts Payable or above Pre requisites : Bcom/Mcom/MBA/CA Inter 5 - 6 years of experience in Accounts Payable Working knowledge of SAP (Mandatory) Media Background (Preferable) Well versed in MS-Office and Current Accounting Environment Knowledge of Foreign Remittances and Accounts Payable Process Ability to lead Team Role Hands-on experience with managing and supervising the accounts payable department and staff in the organization Knowledge applicable Tax Compliances (Like GST, TDS, SEZ, DTAA, etc) Email Communication with Vendors and internal departments for documentation of Foreign remittances Handling Audits Finalisation of books, Audit Schedules Knowledge of Vendor Balance confirmation and MSME Rules Knowledge of Foreign Remittances and Policies Knowledge of GST return filling and working preparation Communication with Banks and HO Finance for foreign payments Ensures that systems, policies, and procedures adhere to company policies while functioning with accuracy and timeliness Vendor / Bank Reconciliations expert Verification of SAP Data for errorless accounting Keep track of the company’s financial expenditures, maintain a database and provide reports as and when requested by supervisors Preparing Power Point Presentation whenever requires Preparing monthly Payables Report Preparing monthly Vendors ageing report Preparing of Audit Statements as per requirements Team player with excellent analytical and communications skills

Principal Task And Responsibilities  Developing validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments  Develop validation documentation for pharmaceutical equipment, facilities and computerized systems.  Having experience in writing, reviewing and executing computer validation documentation (Validation Plan, IQ, OQ, PQ, RTM, summary report).  Experience in any other validations (cleaning, process, etc.), temperature mapping etc.  At least 2 years work experience/exposure to CSV, US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5  Need to have good communication and technical writing skill  PLC System Validation Project - Execution Documentation SCADA Validation Project - Execution, Documentation BMS Validation Project - Execution , Documentation LAB Software Validation  Experience as Administrator for lab Instrument /Equipment Software available in QC.  Managing Administrative activity of GxP Manufacturing Application.  Manage monthly manual backup, Project Creation and periodic preventive maintenance of Lab equipment system.  Manage Active user list , Audit trail , inventory of all instruments and equipment’s  Maintain Document as per IT SOP’S & Performed Administrator related activity for GxP Systems.  Ensure verification of Backup and restoration on periodic basis by centralized backup system. Next Responsible Person: QA Head In the absence of the jobholder, the designee assigned by the reporting manager would be responsible for carrying out the above responsibilities.

Supervision of production & maintenance activities of respective shift. To ensure that every raw material used is of right quality (approved from QC, having reference Number) and quantity (verifying the weights, if required by re weighing) in every batch. To ensure 100% implementation of process conditions for batch as per BPRs. To take instruction from managers for batch charging / monitoring & to execute. To ensure maximum utilization of plant equipment & manpower in respective shift. To report any deviation / discrepancy in plant / process to his to reporting manager. To ensure completion of batches as per plan. To do SAP transaction related to production module. Documentation : To ensure to have online completion documents with respect to his shift. To check critical operation with respect to BPR and to verify the related document. CGMP : To perform verification of pH meters & weighing balance as per SOP. To ensure timely updation of equipment status board Ensure BPRs of ongoing batches are available at specified places near equipment and are online with production. To ensure on line completion of equipment usage log & documentation. To ensure labeling of HDPE / Fiber drums, hose pipes etc. used in respective batch processing. CGMP : To perform verification of pH meters & weighing balance as per SOP. To ensure timely updation of equipment status board

To coordinates of project documentation such as Engineering drawings, Equipment specifications. To monitor status of project to ensure documentation is submitted according to schedule. To review and verifies project documents for completeness, format and compliance with URS. To submit project documentation to management for approval and transmits approved documents to QA. To confer with Engineers, Managers, User and others to discuss project, prepare documents. To execute the report of DQ/IQ/OQ/PQ as per site condition. To ensure and perform Qualification of Equipments as per cGMP norms and as per time schedule. To perform and ensure online documentation. To coordinate with vendors for certificates, drawings and other equipments related documents. To ensure and verification of Utility validation and its documentation online. To prepare MOM during installation and commissioning of equipments at site by vendors. To invite, conduct Equipments operational training of user, Engineering, Project team after successfully commissioned of Equipments. To physically check the Equipment which is installed at site for preparation of Qualification document.