Research Assoc I, R&D - Adl

• Complete method development, validation, and routine stability sample analysis within set timelines.
• Perform testing and data recording for various sample types according to approved methods and pharmacopoeias.
• Operate and calibrate instruments such as HPLC, GC, and pH meters following standard operating procedures.
• Maintain accurate records in logbooks and track the shelf life of chemicals and reagents.
• Adhere to good documentation and laboratory practices, following approved protocols.
• Monitor routine requirements and facilitate timely procurement of necessary materials.
• Investigate and report any deviations or abnormal observations to the sub-department manager.
• Communicate project-related issues and maintain daily work status updates.
• Prepare SOPs and documentation formats, and ensure compliance with regulatory requirements.
• Lead analytical problem-solving efforts and drive process improvement initiatives.
• Implement new techniques and maintain knowledge of relevant regulatory standards.

What Youll Bring

• A degree in M. Pharm or M.Sc. with 6-8 years of proven experience in analytical method development.
• Equal Employment Opportunity
• Baxter is an equal opportunity employer, evaluating applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability, or any other legally protected characteristic.
• Reasonable Accommodations
• Baxter is committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application or interview process due to a medical condition or disability, please reach out to us.
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