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We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. We’re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.

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• To look after the Process Execution job of the project as per the requirement of the organization.
• To install and commission the new machines, equipment and parts and documenting it as per the guideline. E.g. Design Qualification, Installation Qualification, Operational Qualification and performance qualification.
• To study of drawings and evaluating the BOQ for the procurement of materials.
• To analyze OEE reports to find out improvement areas to run the plant in most efficient manner.
• To evaluate new process changes by R&D lab & implementation of same in plants.
• Provide technical support to all GMP Manufacturing processes; IQ/OP/PQ
• Develop manufacturing processes with cross functional groups to enhance and improve overall production
• Recommend, specify and order equipment in support of specific projects including setup and qualification as well as writing and executing qualification protocols
• Write, review and approve SOPs, specifications and other procedure as required
• Analyze, inspect, plan and evaluate use of space and facilities including HVAC systems, computer network wiring lighting and other factors
• Oversee coordination of building space allocation, layout and communication services
• To follow up with contractors for proper execution as per drawing maintaining the quality standards.
• To ensure and maintain the machine and equipment in satisfactory operating condition.
• To Investigate quality failure, process incident and Implementation of effective CAPA with site quality team
• To prepare of P & ID, Process flow diagrams of plant & equipment layouts & data sheets
• To carry out safety studies e.g. SHE Risk Assessment, HAZOP, QRA, JSA (Job Safety Analysis, MSA (Machine Safety analysis, Occupied building report), Quality Studies E.g. Quality Risk Assessment, cGMP design requirements & implementation.
• To keep track on budgeted yield and solvent recovery for meeting budgeted RMC.
• To co-ordinate and carry out development and basic design engineering activities of existing active ingredient.
• To carry out VOC Emission, pollution Load calculations, heat transfer study and heat requirement calculations.
• To eliminate Process Defects & maximize the production.
• To ensure the online documentation of all the relevant records of the department.
• To ensure team building & training to the technicians, operators and production staff for machines in the clean room areas and to attend their queries on immediate basis.

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. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.