This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Ensure the on-time filing of high-quality regulatory submissions, and to assist in the preparation, maintenance, and control of regulatory Dossiers.Interact with all levels in the organization, and across several functions particularly Compliance, Marketing, R&D, engineering, manufacturing, and QA/QC.Participate in discussions to provide strategic regulatory guidance to team members in India and other Region operations.Interact with regulatory agency on regulatory submissions and follow ups of drug products.Oversee the preparation and filing of high-quality submissions to regulatory authorities.Ensure that all applications are filed in accordance with regulations and requirements.Provide regulatory guidance to staff and inter-disciplinary project teams.Be a proactive member of the Regulatory team to ensure Baxter’s continuing compliance with regulatory authorities.Continue to develop quality standards and procedures for RA.Facilitate product development/Launch activities for respective Markets. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. 1.To prepare the media, as and when required. 2. To observe the tubes and plates and to monitor the discarding procedure of the same. 3. To perform periodic microbiological tests as per the schedule, as per Standard Operating Procedure (SOP). 4.To perform the Bacterial Endotoxin Test for product as per the schedule. To perform the bioburden analysis for Raw material and Packing material. 5.To perform bioburden analysis for in process samples 6.To perform enumeration test for biological indicator and Bacterial challenge test. 7.To co-ordinate with technical department for any kind of machine related abnormality, which might be affecting the quality of the product, and its microbiological content. 8.To perform the sterility test for finish product and stability samples as per allotment. 9.To sign all the documents related to microbiological testing. 10.To analyze water samples for Bacterial Endotoxin Test (BET), bioburden, pathogens. 11.To analyze the samples of water system after maintenance work. To maintain and update stock record of all the media and reagents used for microbiological analysis. 12.To update the store person on requirement for procurement and give monthly requirement to Supervisor. 13.To qualify the prepared media for growth promotion test. To perform gram staining of colonies and send them for the identification. 14.To perform the microbiological analysis of stability sample, Finished Product, Raw material, Packaging material, In process as per daily plan of work & in line with standard operating procedure. 15.To perform the validation as per the laid down protocol. To record all the data related to microbiological testing. 16.To prepare requirement list of media & reagent for procurement To intimate Supervisor for any abnormalities in microbiological analysis. However, in the absence of Supervisor, intimate the status of the same to Microbiology Head. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. The person will be responsible for the execution and analysis of analytical work (Method development, and development stability sample analysis) performed at Analytical Development Laboratory, Research & Development, Baxter Ahmedabad. The Person is also responsible to provide an analytical support to Baxter Global, and Baxter’s Contract manufacturing sites. To understand the project in the guidance of Sub-department Manager and follow their instructions.  To perform the analysis under the supervision of Sub-department Manager.  To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed.  To operate and calibrate the instruments as per approved standard operating procedure.  To keep track of each activity related to product analysis and development activities.  To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia. Data recording in ELN and sign off must be completed on time.  To make entry in respective logbook, when start the analysis and at completion of analysis.  To use live reference standards and working standards for analysis and maintain their records.  To verify the shelf life of the chemical or reagent before performing analysis of the material or product.  To follow the Good Documentation Practices.  To update the Development stability compilation sheet after the review of the ELN.  To investigate if any deviation / abnormal observation in term of results and report to Sub-department Manager.  To check the trend of results before reporting the results.  To keep the status of daily work and report to Sub-department Manager on daily basis.  To check Preventive Maintenance, Breakdown maintenance and perform risk assessment and suggest immediate corrective actions as an when required. To report conclusion of preventive maintenance and breakdown maintenance to Sub-department Manager.  To keep track of regulatory commitments.  To use standard formats for documentation.  To update the GLP as per Laboratory requirement as per guidance by Sub-department Manager.  To list out all resources required for the study and keep track of routine requirements and ensure timely procurement of the same, verify the materials received for analysis from supplier as per given requirement.  To verify the instruments after the maintenance.  To complete the trainings as per the quality matrix targets.  To prepare and update the SOPs. To prepare method development and verification report. Administrative:  To perform the work as allocated by Sub-department Manager.  To liaise with customers, staff and suppliers.  To write / fill the record in legible writing.  To keep the documentation online with analysis.  To compile required data for Management Information System and provide to Sub-department Manager.  In the absence of Officer, Sub-department Manager will ensure his roles and responsibilities.  To perform the documentation and QMS related activity using applications software like TCU, Trackwise, etc. Communication to the management / superiors:  To communicate about any failure or abnormal notification or non-complies results to Subdepartment Manager for their attention and seeking for the solution.  To communicate project related issue to Sub-department Manager and follow the action plan.  To keep status of daily work and report to Sub-department Manager on daily basis. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. The person will be responsible for the execution and analysis of analytical work (Method development, and development stability sample analysis) performed at Analytical Development Laboratory, Research & Development, Baxter Ahmedabad. The Person is also responsible to provide an analytical support to Baxter Global, and Baxter’s Contract manufacturing sites. Quality:  To understand the project in the guidance of Sub-department Manager and follow their instructions.  To perform the analysis under the supervision of Sub-department Manager.  To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed.  To operate and calibrate the instruments as per approved standard operating procedure.  To keep track of each activity related to product analysis and development activities.  To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia. Data recording in ELN and sign off must be completed on time.  To make entry in respective logbook, when start the analysis and at completion of analysis.  To use live reference standards and working standards for analysis and maintain their records.  To verify the shelf life of the chemical or reagent before performing analysis of the material or product.  To follow the Good Documentation Practices.  To update the Development stability compilation sheet after the review of the ELN.  To investigate if any deviation / abnormal observation in term of results and report to Sub-department Manager.  To check the trend of results before reporting the results.  To keep the status of daily work and report to Sub-department Manager on daily basis.  To check Preventive Maintenance, Breakdown maintenance and perform risk assessment and suggest immediate corrective actions as an when required. To report conclusion of preventive maintenance and breakdown maintenance to Sub-department Manager.  To keep track of regulatory commitments.  To use standard formats for documentation.  To update the GLP as per Laboratory requirement as per guidance by Sub-department Manager.  To list out all resources required for the study and keep track of routine requirements and ensure timely procurement of the same, verify the materials received for analysis from supplier as per given requirement.  To verify the instruments after the maintenance.  To complete the trainings as per the quality matrix targets.  To prepare and update the SOPs. To prepare method development and verification report. Administrative:  To perform the work as allocated by Sub-department Manager.  To liaise with customers, staff and suppliers.  To write / fill the record in legible writing.  To keep the documentation online with analysis.  To compile required data for Management Information System and provide to Sub-department Manager.  In the absence of Officer, Sub-department Manager will ensure his roles and responsibilities.  To perform the documentation and QMS related activity using applications software like TCU, Trackwise, etc. Communication to the management / superiors:  To communicate about any failure or abnormal notification or non-complies results to Subdepartment Manager for their attention and seeking for the solution.  To communicate project related issue to Sub-department Manager and follow the action plan.  To keep status of daily work and report to Sub-department Manager on daily basis. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Baxter Pharmaceuticals R&D is seeking a highly motivated scientist with proven expertise in liquid chromatography and mass spectrometry to join its Characterization team. As a key contributor within the Pharmaceuticals Global Business Unit, the successful candidate will apply state-of-the-art technologies in LC-MS and GC-MS in support of new and existing pharmaceutical products. The scientist in this role will support Nitrosamine studies (core), extractables and leachable studies, using mass spectrometry-based approaches to identify nitrosamines, potential leachables from container extracts and develop and validate LC/MS methods to quantify NA impurities and leachable compounds in finished drug product solutions. The candidate is expected to work independently in the laboratory, to design studies, conduct independent experiments, and generate and interpret data to solve challenging analytical problems. What you'll be doing Perform chemical extractions of container closure systems and drug product solutions in the laboratory. Apply state-of-the-art mass spectrometry-based approaches to solve challenging problems. Develop and validate novel mass spectrometry-based analytical methods and transfer to other locations (of Baxter/CRO) With the help of SME/Supervisor: plan, execute, and manage projects/programs that both span multiple disciplines and utilize established methods, techniques, or approaches. Prepare/propose technical feasibility of complex design concepts within area of expertise; advise management regarding appropriate action. Interpret data, evaluate analytical results, identify trends/exceptions relative to product requirements, definitions, and/or project goals. Reach conclusions based on research analysis and incorporate recommendations into larger projects. Share research outcomes and methodology with team members and other divisional personnel. Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development to ensure compliance in all research, data collection, and reporting activities. Maintain an in-depth knowledge and understanding of GxP and related regulations and guidance. Be able to provide insights into such regulations so as to facilitate efficient product registration. Be an active participant in the review, adoption, and interpretation of such regulations. Work with third party labs to complete the business deliverables on time. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Major Roles & Responsibilities: Ensure all daily GMP inventory and storage tasks are accurately performed and documented as per SOP and batch record requirements on a timely basis. Report non-conformances immediately to the reporting manager. Ensure that current SOPs and standard formats are used for executing Store work tasks and meet company and international regulations. Supervise verification of Store area tasks in a manner to be ready every day for a regulatory inspection visit or internal/external audits. Ensure the integrity and status of all inventory items at all times. Be vigilant and walk through department daily to verify all items are located and maintained properly. Assure that Technical department has completed PM and/or BM tasks associated with Stores equipment and acts to minimize downtime to department operations. Verify that warehouse areas (rooms, coolers, etc.) are maintained in a constant state of compliance for temperature conditions and any other required environmental criterion. Verify the quantities received against the vendor documentation. Report any discrepancies to reporting manager. Ensure the timely entry of incoming material receipts in the respective system, and clear the associated Goods Receipt Inspection Note (GRIN). Confirm that quarantine labels are affixed and inventory has been transferred to the appropriate quarantine storage area. Upon completion of inventory verification and ID tasks, ensure Quality Control department personnel are promptly notified and provided a Goods Intimation Slip so that required sampling / analysis of materials can proceed. Ensure all incoming receipts of inventory are appropriately identified with complete labeling prior to moving them to a defined storage location. Make certain the Store warehouse properly segregates inventory of different status, per SOP requirements. This includes rejected and hold materials which must be in locked areas to prevent their inadvertent usage prior to their final disposition and/or destruction. Confirm the accurate and timely maintenance of inventory documentation to include electronic records in ERP system (SAP), bin-cards (for housekeeping items), logbooks, registers (for psychotropic products), and files which also fully address all statutory documents. Verify the consistent housekeeping and maintenance of Store facility areas – walls, doors, flooring, dock doors, dock levelers, rodent traps, insecticutors, etc. are regularly cleaned and maintained in a good manner. Ensure materials are accurately issued per batch manufacturing record (BMR) and batch packing record (BPR) and other department (e.g.: Stability) requirements. Check material inventories each day to anticipate and resolve potential inventory shortages. Confirm that FIFO (first-in, first-out) inventory practices are routinely followed in selecting inventory to issue from Store. Closely oversee that any expired material, or material that otherwise has been designated as not valid, is not issued for further use in the manufacturing or distribution process. Ensure any materials deemed discrepant are appropriately identified as such, with status tags clearly designating their status. Make sure that rejected materials are moved immediately to the designated reject storage room in the presence of a QC staff member. Prepare a destruction decision note for this material after securing approval from QA. Verify that rejected material is promptly destroyed by Store department personnel after approval of destruction note by Head of Manufacturing, and the destruction is witnessed by IPQA personnel. Confirm that inventory system records for discrepant materials are promptly updated to reflect their status, with assurance the inventory would not be available for allocation to a production batch or commercial customer requirement. Take special care in re-inventorying partial containers of inventory, where procedurally allowed. Re-verify that correct quantity calculations were made and applied to affected lots/containers. To ensure and record all the activities in the approved formats at the time of observation/activity is performed. To have thorough knowledge of SOP of own working area and ensure to practice it. Ensure that the PM, calibration and validation of equipment/system/facility is completed as per approved schedule. Ensure the housekeeping of the area is in controlled state. Ensure all safety norms are followed in respective area. Keep self and team updated about CGMP requirement. Ensure completion of all required training for self as well as team.x Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To ensure and carry out the analysis of sample and all other activities as per Standard Operating Procedure (SOP). To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside lab. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To operate the Injectable Packing Machines viz. automatic visual inspection machine, leak test machine, labeling Machine, automatic blister & cartonator machine, checkweigher, Track & trace etc. To strictly adhere to the standard operating Procedures and good documentation practices. Troubleshooting of packing area equipment in co-ordination with Maintenance team. Should have good hands on machine changeover Knowledge of SAP and preparation of Mater Documents like SOP, BPR Complaint handling Should be Familiar with Packing Operations of injectables. Experience on device Operation and Pharma Packaging Sound Knowledge of equipment operation & maintenance. To ensure that machines are working smoothly and performing as per standards. To ensure that the packing activities are being performed as defined in the Standard Operating Procedure (SOP) / Batch Packing Record (BPR). To check the status label of packing material prior to take material in packing line. To ensure status labeling to avoid mix-up. To check & verify the rejection generated during packing are being handled as per SOP. To ensure the GMP norms are followed and maintained throughout the packing. To train personnel for the critical operations like visual inspection and labeling. To perform operations like cleaning of packaging equipment, documentation of area, area clearance, line clearance, Status board update. To ensure safety features of all machine is working properly & peoples are using respective personal protective equipment during operation. To follow Standard Operating Procedure (SOP) during entry and exit to plant. To ensure that the preventive maintenance of machine is performed regularly and timely. To report to technical department regarding any kind of maintenance work or any requirements of parts well in advance. To do the replacement of change parts and trial of machine within the time line. To preserve the change parts in good condition and check periodically Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Job Description 1.To prepare the media, as and when required. To observe the tubes and plates and to monitor the discarding procedure of the same. 2.To perform periodic microbiological tests as per the schedule, as per Standard Operating Procedure (SOP). 3.To perform the Bacterial Endotoxin Test for product as per the schedule. To perform the bioburden analysis for Raw material and Packing material. 4.To perform bioburden analysis for in process samples. To perform enumeration test for biological indicator and Bacterial challenge test. 5.To co-ordinate with technical department for any kind of machine related abnormality, which might be affecting the quality of the product, and its microbiological content. 6.To perform the sterility test for finish product and stability samples as per allotment. To sign all the documents related to microbiological testing. 7.To analyze water samples for Bacterial Endotoxin Test (BET), bioburden, pathogens. 8.To analyze the samples of water system after maintenance work. To maintain and update stock record of all the media and reagents used for microbiological analysis. 9.To update the store person on requirement for procurement and give monthly requirement to Supervisor. To qualify the prepared media for growth promotion test. 10.To perform gram staining of colonies and send them for the identification. 11.To perform the microbiological analysis of stability sample, Finished Product, Raw material, Packaging material, In process as per daily plan of work & in line with standard operating procedure. 12.To perform the validation as per the laid down protocol. To record all the data related to microbiological testing. To prepare requirement list of media & reagent for procurement 13.To intimate Supervisor for any abnormalities in microbiological analysis. However, in the absence of Supervisor, intimate the status of the same to Microbiology Head. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Job Description In Process Quality Assurance Activities i.e Line Clearance, FP Sampling, Shop Floor Compliance To take instructions from Supervisor and shift lead to perform the shift activity. To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records. To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR. To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances to shift lead and supervisor and ensure appropriate actions (CAPA) in place. To collect In-process samples, finished product samples, and other samples timely submission into QC/micro. To review and verification of electronic records/Audit trails and printout of the equipment’s like autoclave, sterilizer, filter integrity machine and any other equipment’s etc. To ensure the respective documents to be destructed as per approved procedure. To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured. To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification. To execute the approved Corrective and Preventive Action (CAPA) with in define timeline. To raise Document Change Request (DCR) and Change Control Management (CCM) and track the same and ensure closure as per Standard Operating Procedure. To prepare and review the SOPs. To carry out stagewise BMR review for batch execution compliance. To track the CPV Program through provided exhibits and to prepare the Minitab files for required products based on production plan for the month. To collect the data related to CPPs/ CQAs and shall perform data analysisy. Report any abnormality gap to supervisor /Shift lead. To maintain the admin logins for all applicable equipments and to provide the new logins, activation & deactivation for users and periodic verification & access control of all users. Initiation of batch number in BaxLIMS after proper verification of manufacturing and expiry date and correction of entries if required. To approve the preventive maintenance activities in MAXIMO and risk assessment review and approval. To ensure the handover of shift-to-shift activities and record in Shift charge Handover format/logbook. To communicate about any failure or abnormal notification to Supervisor & shift lead for timely escalation and resolution. To Perform impact assessment of breakdown maintenance and approve activity in MAXIMO and risk assessment review. Material A.R.No. Stock Blockage or Un-blockage in System. To perform the periodic building inspection with Admin team. Any other responsibility assigned by shift lead and reporting manager. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Sr, Spec, Quality - Compliance  To perform internal quality audits to ensure the compliance to all systems and procedures and ul􀆟mately build the quality focused and ensure appropriate CAPA is placed.  To ensure that system and facili􀆟es comply as per the regulatory requirements and expecta􀆟ons.  To ensure cGMP compliance status of site as per regulatory requirements.  To ensure and sustain all 􀆟me ready plant in line with current regulatory expecta􀆟ons for regulatory authori􀆟es and other partner inspec􀆟on.  To verify process and systems are complying standard opera􀆟ng procedures (SOPs) and current regulatory requirements and expecta􀆟ons.  To ensure that audit observa􀆟on compliance and effec􀆟veness of CAPA.  To perform external audit related process.  To perform GEMBA round of site and report in case of any non-conformance observed during round.  To perform periodic assessment of the GMP trends.  To perform the assessment of regulatory intelligence program and global observa􀆟on cer􀆟fica􀆟on.  To ensure that the required ini􀆟al and con􀆟nuing training of personnel is carried out and adapted according to need.  To impart training to personnel regarding enhancement in regulatory guidelines, system, and processes.  To handle electronic QMS modules for review and approval of changes, procedures etc. To ensure that data integrity is being maintained at all level and to perform / get performed regular checks to ensure that system is in state of control. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To prepare and review manufacturing investigations related to NCR /OOS/OOT/OOL/market complaints to identify the root cause and implementation of appropriate CAPA. To prepare and review risk assessment for associated QMS element & ensure completion of risk assessment in timely manner. To initiate and review Change Control for any changes, execution and Change Control closure in timely manner. To handle and review Document change request/ Change control and impact assessment of the cross functional department. Handling of QMS activities in Track wise software. To prepare and review Standard Operating Procedure (SOP), Exhibit, Standard Format in TcU and ensure the documents are in line with current Good Manufacturing Practice (cGMP) requirements To escalate any delay in investigation or QMS elements to supervisor & ensure closure of the same within defined timeline. Tô complete training on assigned SOPs in BAXU system in timely manner & ensure completion of such training completion by team and coordinate with Training and Development department for initiation, effectiveness, and closure of training. To track all open QMS elements & ensure closure of such elements with effective CAPA within defined timeline. To check data integrity & compliance of all processes & systems is being maintained at all levels by frequent GEMBA. To face internal or external current Good Manufacturing Practice (cGMP) regulatory audits & respond to the auditors’ queries. Also ensure audit preparedness in the function. To inform supervisor/individual regarding a safety/ Hazard concern in area. To perform task assigned by department head time to time. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To ensure wearing the PPEs while working in routine operation/maintenance of any machine as per requirements and inform supervisor/individual regarding a safety/ Hazard concern in area. 2.2 To adhere with current Good Manufacturing Practice(cGMP), Good Document Practice (GDP), Standard Operating procedure (SOP) & Data Integrity Principles i.e., ALCOA+. 2.3 To ensure cleanliness and environmental norms of clean room and ensure availability of clean room garments and goggles. 2.4 To ensure clean room behaviour and entry exit procedure followed as per Standard Operating Procedure. 2.5 To ensure that all activities carried out in compliance mode and implement cGMP norms on a continuous basis in the production area. 2.6 To perform the batch filling operation as per Standard operating procedure. 2.7 To perform and ensure CIP & SIP process is carried out as per validated procedure. 2.8 To perform and ensure cleaning and disinfections of floor, ceiling, wall, pipeline, vessels, and equipment as per frequency defined. 2.9 To ensure the machine is working smoothly and it is performing well producing desired standards. 2.10 To ensure the status tags are displayed properly. 2.11 To co-ordinate with engineering department for the plant related repair, preventive maintenance, EMS/BMS excursion and communicate for any utility or technical problems to concern department to avoid the production loss or any quality issue. 2.12 To communicate with chemist and supervisor for production activity/ plan, rejection and break down. Any quality related issue is found in the product, escalate to Supervisor and Line Manager, and rectify as per SOP. 2.13 To stop the activity if any non-conformance found in activity and inform to superior. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Safety: Compliance to SOP’s and practicing utmost safety standards to ensure Industrial safety. Implementing safety initiatives in all areas of engineering and monitoring the results. Equipment Maintenance: To ensure the Preventive Maintenance (PM) of Production equipments like Ampoule Filling Equipments, Vial Filling Equipments, Sterilizer, Autoclave, Manufacturing and Holding Vessels etc. as per Preventive Maintenance Planner and should have exposure with computerized maintenance management system. To carryout Breakdown Maintenance (BM) work in the Production equipments. Person should have hands-on experience of preventive and breakdown maintenance of Packaging equipments. Person should have operation and maintenance exposure in Clean Water System equipments like WFI Generation & Distribution System, Pure Steam Generation System etc. Hands on experience on HVAC, EMS/BMS will be an added advantage. Equipment Operation: Person should have hands-on experience of operation of Water System Equipments system. Person should have hands-on experience of work with different make VFD, HMI and PLC. Enough Technical knowledge required on different critical production equipments used in injectable facility. To prepare a system for efficient utilization of available resources leading to cost optimization. Technically well versed on different critical production equipments used in injectable facility. Person should have knowledge of clean room maintenance practice. Person should have knowledge on different types of atomization. Documentation (QMS): To prepare & review all the documents related to operation, preventive maintenance, breakdown maintenance and new machines installation. Person should have knowledge of QMS element like CAPA, CCN, Deviation, and Deviation Investigations Report and tools for investigation. Project: Person should have hands-on exposure of new installation of different production and water system equipments. Person should have hands-on exposure of commissioning activity of critical production equipments. Validation / Qualification: Person should have experience of Validation and periodic qualification for different production equipments. Person should have hands-on experience of prepare and review of validation documents of new equipment. Person should have hands-on exposure of Computer System Validation (CSV). Person should have knowledge of cGMP requirements. Other: To maintain working area as per 6S standards. To perform GEMBA periodically and resolve all observation related to GEMBA. Person should be able to operate equipments at maximum efficiency. Person should have hands-on work experience of Energy conservation techniques. Coordinate with manufacturing to ensure manufacturability of products while maintaining quality, safety and environmental standards and achieving cost targets in a timely manner. Work collaboratively, negotiate and engage with key stakeholders to facilitate delivery and compliance with the engineering strategy. Able to take care of any additional activity given by superior as & when required. Person should able to effectively utilization of manpower. Person should have effective management skill of different maintenance work during shift. Person should have key behaviour attributes like communication skill, orientation skill, presentation skill, analytical skill and problem solving skill. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Roles & Responsibilities: 1. Effectively manage and process complaints and MDRs , which includes performing daily tasks associated with process 2. Opening of complaints 3. Collecting necessary complaint information 4. Performing follow up with the customer (written and verbal) 5. Determining reportability of complaints 6. Creating associate Regulatory reports (eg; MDRs) per regulations 7. Evaluating complaints for need to investigate and coordinating sample retrieval 8. Responding to customer complaints (written) 9. Timely closure of complaints, as per procedure. 10. Effectively manage workflow, identifying issues 11. Participate in continuous improvement, efforts and projects, as assigned Education: Bachelor’s degree or equivalent education required Required skills: Good Communication Skills in English (written and verbal) Capable of working in highly- regulated environment Proficient with basics in MS -OFFICE Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To ensure the line clearance of packing before starting the packing of new batch in coordination within Process Quality Assurance Chemist. To ensure the issue of material of the batch and taking the clearance from the In Process Quality Assurance Chemist, prior to schedule of respective product packing. To online the updation in the packing records. To provide the data to transfer the packed goods to the finished goods store in coordination with Manager Manufacturing. To ensure the timely packing of unpacked goods from the General Quarantine area. To supervise the packing online at frequent intervals as defined in the Standard Operating Procedure. To ensure the availability of packing material with proper labels and status. To do the reconciliation after completion of batch and submitting the data of the same. To keep the samples of each packing batch as per Quality Assurance and Quality Control requirement. To destroy the rejection generated during packing in presence of In Process Quality Assurance Chemist. To keep the status tags displayed properly so that the status of each material issued and packed is maintained as per the regulatory requirement and Standard Operating Procedure. To set and arrange the trained worker force according to norms to get the highest productivity and quality packing. To ensure the GMP norms are followed and maintained all throughout the packing. To train the work force for critical operations like visual inspection and labelling. Education & Qualification- Pharmacy Graduate with 2 - 6 Years working experience in injectables packing lines. Must have experience in Automatic Visual inspection. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To perform the cleanliness of area and machines before starting the mixing process. To perform CIP/SIP of machine before commencing the filling activity. To perform availability of all raw materials including WFI required for the mixing activity. To perform availability of Batch manufacturing record before commencing the mixing activity. To perform the compliance of environmental conditions before commencing the mixing activity. To perform the line clearance from IPQA before commencing the mixing activity. To run the machine as per approved SOP and in compliance with cGMP To record all the activities in the approved formats at the time of observation/activity is performed. To escalate to supervisor for any non compliance and breakdown Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To perform and control Filling and mxing activirty Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Filling Operator To ensure wearing the PPEs while working in routine operation/maintenance of any machine as per requirements and inform supervisor/individual regarding a safety/ Hazard concern in area. To adhere with current Good Manufacturing Practice(cGMP), Good Document Practice (GDP), Standard Operating procedure (SOP) & Data Integrity Principles i.e., ALCOA+. To ensure cleanliness and environmental norms of clean room and ensure availability of clean room garments and goggles. To ensure clean room behavior and entry exit procedure followed as per Standard Operating Procedure. To ensure that all activities carried out in compliance mode and implement cGMP norms on a continuous basis in the production area. To perform the batch filling operation as per Standard operating procedure. To perform and ensure CIP & SIP process is carried out as per validated procedure. To perform and ensure cleaning and disinfections of floor, ceiling, wall, pipeline, vessels, and equipment as per frequency defined. To ensure the machine is working smoothly and it is performing well producing desired standards. To ensure the status tags are displayed properly. To co-ordinate with engineering department for the plant related repair, preventive maintenance, EMS/BMS excursion and communicate for any utility or technical problems to concern department to avoid the production loss or any quality issue. To communicate with chemist and supervisor for production activity/ plan, rejection and break down. Any quality related issue is found in the product, escalate to Supervisor and Line Manager, and rectify as per SOP. To stop the activity if any non-conformance found in activity and inform to superior. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. 1. To ensure wearing the PPEs while working in routine operation/maintenance of any machine as per requirements and inform supervisor/individual regarding a safety/ Hazard concern in area. 2. To adhere with current Good Manufacturing Practice(cGMP), Good Document Practice (GDP), Standard Operating procedure (SOP) & Data Integrity Principles i.e., ALCOA+. 3. To ensure cleanliness and environmental norms of clean room and ensure availability of clean room garments and goggles. 4. To ensure clean room behaviour and entry exit procedure followed as per Standard Operating Procedure (SOP). 5. To ensure that all activities carried out in compliance mode and implement cGMP norms on a continuous basis in the production area 6.To perform the batch capping operation as per Standard operating procedure. 7. To perform and ensure cleaning and disinfections of floor, ceiling, wall, pipeline, vessels, and equipment as per frequency defined. 8. To ensure the machine is working smoothly and it is performing well producing desired standards. 9. To ensure the status tags are displayed properly. 10.To co-ordinate with engineering department for the plant related repair, preventive maintenance, EMS/BMS excursion and communicate for any utility or technical problems to concern department to avoid the production loss or any quality issue. 11. To communicate with chemist and supervisor for production activity/ plan, rejection and break down. Any quality related issue is found in the product, escalate to Supervisor and Line Manager, and rectify as per SOP. 12.To stop the activity if any non-conformance found in activity and inform to superior. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less