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. Essential Duties and Responsibilities. Quality: To conduct development trials as per requirement. To compile & evaluate the development & stability data. To ensure development trails to be performed as per Quality By Design (QBD) approach. To prepare the technical documents e.g. Master Formula Record (MFR), Product Development Report (PDR), Product Development Lifecycle Management (PDLM) documents, Protocols & Reports. To provide required information for meetings with cross functional teams like Analytical, Regulatory, PSM, Product Quality, manufacturing, Contract Manufacturing Organization (CMO), Project management for on time project delivery. To provide required information for meetings with Contract Manufacturing Organizations (CMO), Contract Research Organizations (CRO) & contract Labs for on time project delivery. To support in execution of stability batches in Baxter sites & CMOs. To support for Process validation and commercial batches. To provide support for successful technology transfer of drug products at manufacturing plant & Contract Manufacturing Sites. To review engineering batch & stability batch documents. To collect the Stability batch data and review for trending and conduct review of artworks. To support sub-department manager to review the technology transfer documents for products developed by CRO & assess the documents which are in-line with QBD based approach & as per current regulatory requirement. To perform the required activities for remediation projects to fulfill the regulatory commitments for Out of Specification or Project Change Control Notes or Corrective and Preventive Action or product nature and criticality. To perform the required activities to fulfil the regulatory submission & query requirements. To prepare the reports to be provided for regulatory response. To handle trouble shooting during exhibit and commercial batches with an ability to investigate any Out of Specification (OOS) or Out of Trend (OOT) results. To interact with the plant team and impart new product introduction prior to start of production. To support External and Internal regulatory audits with respect to Manufacturing Process. To support for market complaint related activities. To possess and be updated on product submission and knowledge in regulatory market, current guidelines i.e. ICH (International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use), US-FDA (United States Food and Drug Administration), MHRA (Medicines and Healthcare products Regulatory Agency), EMEA (European Medicines Agency) etc. To identify & make available the necessary required resources or infrastructure or instruments to carry-out the day-to-day functions and ensure entire documentation related to formulation development & execution of batch. To assist Sub-department Manager & Department Head in investigation for complaints and deviations. To analyze investigation, to suggest any further actions required, to conclude root cause and to seek approval of Corrective and Preventive Action (CAPA) from Department Head. To prepare change control and ensure timely closure of the same. To ensure compliance related to Lab equipment, instruments, documentation & warehouse. To prepare and file change control for updation of SOP and send for further review of Sub-department Manager & approval of Department Head. To document experiments in Electronic Lab Notebook (ELN). To identify & request for New Equipment's or instruments for projects in upcoming portfolio & continuous improvement of Development Lab. To adopt & follow the Global Quality procedures. To identify the safety hazards & perform the Hazard Identification Risk Assessment (HIRA) in coordinates with EHS (Environmental health and safety) practices at place. Administrative: To work collaboratively in cross-functional teams. To liaise with customers, staff and suppliers for material procurement or query related or any other work. To review the entries in logbooks. In the absence of Executive, Sub-department Manager will ensure these roles and responsibilities. Authorities for rejections or approval: To hold the projects due to lack of resources as per guidance by Sub-department Manager. To take decision for non-compliance results as per guidance of Sub-department Manager. Communication to the management / superiors: To communicate with sourcing team if any information requires from suppliers. To communicate with cross functional team if any information required for product development. To communicate about any failure or abnormal notification or non-compliance results to Sub-department Manager & Department Head for their attention and seeking for the solution. To communicate project related issues to Sub-department Manager and implement action plan under the guidance of Sub-department Manager. Qualifications : Educational Qualification: Master’s in pharmacy / Pharmaceutics Master’s degree with 8-15 years pharmaceutical experience. Writing and computer skills relevant to recording original data as well as creating protocols, reports, and presentations to communicate with partners and team members. The ability to energetically attack a problem and synthesize the results into a clear and logical summary in a timely manner is critical. Subject matter expertise in areas associated with modern formulation instrumentation. Ability to learn and master new development strategy and develop new methods where appropriate. Communication skills to build relationships across functional and geographical boundaries and present technical concepts to technical and non-technical teams. Comfort with risk and ambiguity, ability to negotiate critical timelines for analysis in emergency situations. Personal responsibility and independent ownership of analysis and results. Experience with leading large projects and formulation development and technology transfer. A good understanding of ICH and cGxP practice. Experience in working in global cross-functional teams and project management is a plus. Quality oriented. Ability to adapt to changes and to work in a team environment as well as delegate effectively to junior team members. 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. About Us: Baxter's Mission 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. Your Role at Baxter This is where your work saves lives The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate - F&D at Baxter, your work contributes directly to making a significant impact on others. It's exciting work—and you're not on your own. Our teams collaborate cross-functionally and lead by influence. Whether guiding a team through a project or managing direct reports, our research and development team is responsible for influencing others to achieve results. Our colleagues within our R&D organization desire to work on products that make a meaningful difference in others' lives. We are motivated by the power of teamwork and are natural leaders who are skilled at influencing others. When you join Baxter as a Research Associate - F&D, you'll use your analytical approach to identify risks and opportunities for innovation quickly. Agile and willing to take action, you stay calm under pressure. What you'll be doing ! Provide support to the Formulation team in technical and operational activities. Complete QbD-based experiments to develop pharmaceutical injectables. Interpret and record analytical results and laboratory work per Baxter's GDP. Conduct literature searches and compile reports for respective products/projects. Engage in root cause analysis and propose innovative solutions. Assist in the scale-up and technology transfer of injectable products. Ensure compliance with Baxter’s Quality Manual, SOPs, and EHS&S guidelines. Collaborate with collaborators, customers, partners, and team members to meet project commitments and quality standards. What you'll bring ! Ph.D./M.Pharm in a relevant scientific field (Pharmaceutics) or equivalent experience of 4-6 Yrs. Basic understanding of instruments, formulations, and regulatory guidelines. Work experience in injectable formulations, including complex injectables. Proven research papers and patents in high-impact journals. Hands-on experience in formulation and development. Outstanding problem-solving skills, adaptability, and innovative mentality. Excellent written and verbal communication skills in English. Ability to work effectively within a team and independently. Strong organizational and prioritization skills to meet project deadlines. Collaborative and inclusive attitude with a focus on continuous improvement. Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy 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. 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.

MFG Production (B.Pharm /B.Sc/ITI): Positions- Operator, Sr Operator & Chemist 3 to 8 Experience in Injectable production, mixing(batch manufacturing), filling, dispensing, sterilization, autoclave, batch record review etc., activity MFG Packing (M.Pharm/M.Sc/B.Pharm /B.Sc): 3 to 8 Experience in Injectable packing activity. automatic visual inspection machine operation, kit preparation, VIT operator training & qualification, batch record review, etc., activity Interested Candidate can apply on link below: https://forms.gle/ffSMoroai6sYkJHr6

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. 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. Other: To maintain working area as per 6S standards. Person should have hands-on work experience of Energy conservation techniques. Able to take care of any additional activity given by superior as & when required. Person should have key behaviour attributes like problem solving skill, technical sharpness etc. 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. To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification. To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Supervisor regarding any non-conformity from planning and execution. To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Supervisor and approved by Manager. To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Trackwise. To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date. To ensure samples withdrawal during process validation & keep Supervisor updated about any non-conformity. To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents. To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by Supervisor. To attend trainings of each protocol before execution of any validation and qualification activity. To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA. To update the protocols as per current regulatory requirement to improve the validation documents. To prepare VMP as per regulatory guideline or any audit compliance requirement and provide it to Supervisor for review & approve. To keep the validation document updated from GMP aspect as per regulatory expectation. Planning and execution of validation activities associated with QMS elements. To inform the activity or issues which might occurred during the shift's validation activities through daily meeting. To review and approve the documents related to Validation activities and other documents related to Operation. To assist/participate during internal or external inspection. Timely completion of assigned trainings. To be vigilant for safety aspects and record hazard or any near miss in the provided portal. Any additional responsibility as assigned by the Supervisor. 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. To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification. To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Supervisor regarding any non-conformity from planning and execution. To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Supervisor and approved by Manager. To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Trackwise. To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date. To ensure samples withdrawal during process validation & keep Supervisor updated about any non-conformity. To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents. To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by Supervisor. To attend trainings of each protocol before execution of any validation and qualification activity. To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA. To update the protocols as per current regulatory requirement to improve the validation documents. To prepare VMP as per regulatory guideline or any audit compliance requirement and provide it to Supervisor for review & approve. To keep the validation document updated from GMP aspect as per regulatory expectation. Planning and execution of validation activities associated with QMS elements. To inform the activity or issues which might occurred during the shifts validation activities through daily meeting. 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. 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.

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. In this role as an Eng II, V&V, you will be responsible for ensuring the flawless quality and performance of our innovative medical products. Your consistent attention to detail and commitment to excellence will be instrumental in guaranteeing that our products meet world-class standards. You will collaborate with a diverse team of dedicated individuals, working together to successfully implement and compete in the rapidly evolving healthcare industry. Responsibilities: Collaborate with diverse teams to determine product requirements and specifications. Design and develop test plans and protocols for the verification and validation of products Conduct testing, analyze data, and identify areas for improvement Ensure flawless execution of testing procedures and documentation Successfully implement continuous improvement initiatives to enhance product quality Compete in a fast-paced environment and meet project deadlines Demonstrated skill in effectively addressing and resolving technical challenges Requirements: Bachelor's degree in Engineering or related field 5+ years of experience in engineering role, preferably in the medical device industry Strong knowledge of verification and validation principles and methodologies Proficiency in using testing tools and equipment Exceptional attention to detail and ability to work with complex data sets Ambitious and self-motivated with a passion for innovation At Baxter, we foster an inclusive and collaborative work environment where every individual's contribution is valued. We are an equal opportunity employer, embracing diversity and providing equal employment opportunities to all qualified applicants. Baxter is committed to providing reasonable accommodations to individuals with disabilities globally. If you need a reasonable accommodation during the application or interview process, please let us know by contacting us through the provided link. Apply now and join us in saving and sustaining lives. 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. 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.

"Hiring Event Announcement" MFG Production Operators (ITI): 3 to 8 Experience in Injectable production, filling, dispensing, sterilization, autoclave, batch record review etc., activity MFG Packing Operators ( ITI): 3 to 8 Experience in Injectable packing activity. Date & Time : 31st May 2025 || 09 AM to 3 PM IST Venue : Ahmedabad (Invites will be shared based on your shortlisting) Registration Link copy : https://talentcommunity.baxter.com/flows/manufacturing-packing-operators-31st-may-25-gqengvlfs EEO (Equal Employment Opportunity) This is where Baxter International Inc. is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Role & responsibilities Actively supports launch and sustenance of Baxter commercial product globally. Support all commercialized project related requirements related to Baxter manufacturing sites and CMOs Globally. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of product design governance documents for a particular product family. Make sure the relevant documents for various product families are available to support risk management, change control processes and design integrity. A very good understanding of Quality Risk Management for pharmaceutical products is required per ICH Q9 and ensure sustenance of Baxter commercial products globally by following Baxter Quality Management Systems. Respond to customer queries regarding safety aspects of the product after consultation with Clinical affairs and other relevant functions. Manage Platform core team performance, product life cycle, project schedule, execution, budget commitments and spend. Review weekly, monthly/yearly progress of the projects and send report to the governance team to implement the improvements suggested by the governance. Drive the discussion and ensure the implementation of VIP/ MIP projects, alternative vendor projects. Own supplier notification of change (SNC) or change control to support the implementation of change on time. Preferred candidate profile Educational Qualification: Masters in Pharmaceutics or equivalent Data Analysis and Good communication skills for effective liaison and teamwork Problem-solving skills, analytical skills and attention to detail Excellent organizational skills and the ability to work on several tasks or projects concurrently Presentation skills - for presenting ideas and findings to colleagues and customers Ability to work well independently, with minimum supervision Drive, enthusiasm and self-motivation An aptitude for mathematics and statistics and highly developed IT and technical skill Project management skills and having knowledge of MS office and project management tracking software (Microsoft project, primavera and Planisware) to track and monitor the project progress will be an added benefit.

Essential Duties and Responsibilities: Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family. Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis. Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation. Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety. Provide support to analytical team by providing the required product solution/placebo solution samples. Execute batches in laboratory, assess the study outcome to support the compendial product change requirement. Ensure response to customer queries, agencies query, market compliance. Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance. Responsible for ensuring the availability of required licenses and materials (raw material, packaging materials) in laboratory. Qualifications: Educational Qualification: Masters in Pharmaceutics or equivalent Hands on experience in laboratory batch execution and drive the towards the expected result. Good communication skills for effective liaison and teamwork Problem-solving skills, analytical skills and attention to detail Excellent organizational skills and the ability to work on several tasks or projects concurrently Presentation skills - for presenting ideas and findings to colleagues and customers Ability to work well independently, with minimum supervision Drive, enthusiasm and self-motivation

Role & responsibilities To monitor and lead various Packing departmental activities in respective shifts. To adhere with current Good Manufacturing Practice(cGMP), Good Document Practice (GDP), Standard Operating Procedure (SOP) & Data Integrity Principles i.e. ALCOA+. To ensure packing plan execution as per the provided monthly plan and ensure the availability of material, prior to schedule of respective product packing. To ensure availability of Batch Packing Record (BPR) for execution as per plan, to review & ensure submission of executed Batch Packing Record (BPR) to QA. To ensure that the packing & packing associated activities are being performed as defined in the Standard Operating Procedure (SOP) / Batch Packing Record (BPR). To ensure respective packing stages entry/trending of respective stage rejections and good containers done as per SOP. To ensure & plan for training, periodic training and retraining for staff or workers as per requirement. Also authorize & train workers for packing activity and VIT and ensure the individual training completion in stipulated timeframe. To perform/participate the non-conformance investigation, CAPA implementation & CCM execution of packing area and ensure the closure of the same in defined timeframe. To perform GEMBA round of department & ensure escalation & closure of any abnormalities in line with Standard Operating Procedure (SOP). To communicate any abnormality related to packing material and change in planning to Manager, prior to start of the activity. To ensure the timely packing of unpacked goods from the General Quarantine (GQ) area. Preferred candidate profile Pharmacy Graduate with minimum 9 yrs of experience in Parenteral Packing Job Location : Baxter Pharmaceuticals India Private Limited Sarkhej-Bavla Road, Chacharvadi-Vasna, Ahmedabad, India