Job Description

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\xe2\x80\x94where your purpose accelerates our mission.

• 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 to Sub-department Manager if any deviation or issues observed.
• To operate and calibrate the instruments as per approved standard operating procedure.
• To keep the track of each activity related to product analysis.
• To carry out all the testing and data recording according to the approved SOPs and current pharmacopoeia.
• 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 follow the instruction and procedure as mentioned in the approved development protocol.
• To keep track of routine requirements and ensure timely procurement of the same.
• 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. To report conclusion of preventive maintenance and breakdown maintenance to Sub-department Manager.
• To keep track of regulatory commitments.
• To prepare 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.

Administrative:

• To perform the work as allocated by Sub-department Manager.
• To liaise with customers, staff and suppliers.
• To respond the query in the stipulated time line.
• 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.

Communication to the management / superiors:

• To communicate about any failure or abnormal notification or non-complies results to Sub- department 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.
• Qualifications.
• Master in Pharmacy / Science with more than 10 years of Experience.
• Key technical skills:
• Thorough understanding of Method Development, Stability Studies, Method Validation and Transfer.
• Basic Knowledge of Chemical Analysis,
• Knowledge of pharmacopoeia, ICH Guidelines
• Operational and Calibration of Instrument
• Trouble shooting of various problems obtain during the product development
• Knowledge of Transfer of Technology
• Knowledge of Good Laboratory Practice and Good Documentation Practices

Additional

• Key behavioral attributes:
• Communication skills
• Presentation skills
• Analytical skills
• Lateral coordination
• Positive Attitude
• Policy compliance
• Documentation Skills

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.

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