Baxter Research Associate Recruitment

Baxter Research Associate Recruitment – Applications Invited Online

Research Associate II

Req # JR – 133801

Location: Bengaluru, Karnataka, India

Job Category: Research and Development

Date posted: 10/07/2024

Vantive: A New Company Built on Our Legacy

Since last year, Baxter has been on a journey to separate our Kidney Care segment into a standalone company. Vantive will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

This position is responsible for:

  • Conducting laboratory testing, not limited to validation, verification, transfer, and registration stability studies. The successful candidate shall possess solid “hands-on” technical abilities, a passion for their work, and the impact it has on meeting the needs of patients.
  • Effectively contributing technical knowledge and skills to a variety of projects by conducting testing, designing analytical methods and experiments.
  • Interacting effectively with a variety of disciplines (Quality, Regulatory, External partners etc.).
  • Conducting routine research and design experiments, independently developing, evaluating, validating, and/or transferring analytical methods.

Essential Duties and Responsibilities:

  • Collect information for the analytical target profile.
  • Propose techniques and develop analytical methods independently.
  • Design studies and write protocols, reports, and procedures with minimal guidance.
  • Evaluate, validate, or transfer analytical methods, including investigating failed acceptance criteria.
  • Contribute routine scientific knowledge or expertise to research and development activities for achieving project goals.
  • Evaluate current methods and devise new approaches through adaptations and incorporation of new technologies to meet business objectives such as quality and cycle-time.
  • Independently conduct routine research and developmental activities. Plan details of assigned tasks within specific parameters.
  • Employ appropriate techniques and methods to successfully conduct assignments within negotiated deadlines after receiving general instruction.
  • Perform laboratory testing in a regulated environment.
  • Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks.
  • Develop knowledge and understanding of GxP and related regulations and guidance.
  • Conduct R&D stability testing as per the stability protocol to support registration of R&D products.
  • Independently execute analytical method validations and transfers with minimal support.
  • Accurately test the samples (Right First Time) and assess results for conformance to specifications.
  • Manage laboratory investigations (OOS/OOT), Nonconformance/deviations to identify sound scientific root cause and follow up with implemented corrective and preventive actions.
  • Sample receiving and data entry in LIMS.
  • Adhere to cGxP requirements (ALCOA+), Data Integrity, Quality Culture, and Compliance Level.
  • Own SOPs of relevant techniques/procedures.
  • Advise and troubleshoot issues and propose solutions.
  • Maintain lab equipment and report on malfunctions.
  • Have good knowledge of laboratory health and safety standards.
  • Demonstrate the ability to identify risks, issues, and opportunities for improvement of existing processes, technologies, and approaches by providing sound scientific rationale.
  • Maintain knowledge of relevant QSR and other regulatory requirements related to R&D to ensure compliance in all research, data collection, and reporting activities.
  • Collaborate with global teams across various functions (ex. quality, regulatory, operations, manufacturing, etc.).
  • Analyze data, make decisions, and present status at technical review meetings.
  • Design studies and autonomously write protocols, reports, and procedures with minimal guidance.
  • Support in writing responses to authorities’ questions on analytical methods.

APPLY ONLINE HERE

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