Research Associate I, R&D - ADL
Research Associate I, R&D - ADL
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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. Youll feel a sense of purpose throughout the organization as we know our work improves outcomes for millions of patients.
Baxters 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 liveswhere 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 Baxters Contract manufacturing sites.
To understand the project in the guidance of Subdepartment Manager and follow their instructions.
To perform the analysis under the supervision of Subdepartment Manager.
To complete the planned work in the stipulated time frame inform the Subdepartment 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 Subdepartment
Manager.
To check the trend of results before reporting the results.
To keep the status of daily work and report to Subdepartment 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 Subdepartment 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 Subdepartment 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 Subdepartment 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 Subdepartment
Manager.
In the absence of Officer Subdepartment 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 noncomplies results to Subdepartment Manager for their attention and seeking for the solution.
To communicate project related issue to Subdepartment Manager and follow the action plan.
To keep status of daily work and report to Subdepartment 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.
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Required Experience:
IC
Employment Type
Full-Time
