Research Associate, R&D F&D

This is where your work makes a difference.

At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today tomorrow and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together our community is driven by a culture of courage trust and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations and we hold each other accountable for delivering exceptional results.

Here you will find more than just a jobyou will find purpose and pride.

This position provide active involvement and contribution in the Formulation R&D team in terms of technical and operational activities such as hands-on support to formulation development in parenteral formulations and interpretation of analytical results. The incumbent will perform other duties as assigned.

• Literature search for the respective product / project and make a consolidated report.
• Define organize plan and execute QbD-based experiments to develop pharmaceutical injectables in compliance with current international / regional / national regulations with the support of senior colleagues and team members.
• Analysis of the experimental study outcome and present the data to the team for the further action plan.
• Independently analyze and propose solutions to research problems based on understanding.
• Engage in root cause analysis in new product development and sustaining product projects under supervision.
• Understanding of the manufacturing process to assess the impact on the product quality under supervision.
• Apply technical theories and principles to projects within area of expertise.
• Scale up and plant support for technology transfer of injectable products.
• Innovative ideas generation for new project development.
• Document laboratory work performed per Baxters GDP.
• Work according to appropriate standards (e.g. Data Integrity ALCOA) guidelines.
• Follow Baxters Quality Manual SOPs and Environmental Health Safety & Sustainability (EHS&S) guidelines in day-to-day activities to ensure proactive compliance and continuous improvement.
• Provide support as needed in calibration and maintenance of equipment in the laboratory.
• Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders with respect to project commitment quality procedures and business needs

Establish maintain and update technical & Design documentation according to Good Documentation Practices

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.

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

Key Skills

Laboratory Experience,Vendor Management,Design Controls,C / C++,FDA Regulations,Intellectual Property Law,ISO 13485,Research Experience,SolidWorks,Research & Development,Internet Of Things,Product Development

Employment Type : Full-Time

Experience : years

Vacancy : 1