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BAXTER

RA I Product Quality

Early Applicant
  • 11 days ago
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Job Description

This is where you save and sustain lives

nAt 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.

nBaxter'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.

nTogether, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

nJoin us at the intersection of saving and sustaining liveswhere your purpose accelerates our mission.

nJob Summary:

nWe are seeking a highly motivated and detail-oriented Research Associate-II to join our Product quality department at Baxter Pharmaceutical India Pvt. Ltd. As a key member of our team, this position will be responsible for providing subject matter expertise in the areas of failure investigation, Quality System, formulation and Analytical technical documents, technology transfer, and post-approval products. This position will review and approve critical analytical and formulation documents and provide expert advice on cGxP regulations and guidelines. Additionally, this position will collaborate with other functions such as project management, regulatory, analytical, formulation, and CMO to ensure the successful execution of our products.

nResponsibilities:

nMajor responsibilities are as mentioned below but not limited to,

  • nReview and approval of technical documents of GPRD which includes analytical and formulation documents.
  • nPerform tool based investigations for CMO, R&D, plant, and contract labs to ensure compliance with cGxP regulations and guidelines.
  • nReview and approve QMS documents such as change controls, investigations, and audit reports in TrackWise.
  • nHandle market complaints and manage the quality management system (change control, CAPA, deviations, OOS, etc.).
  • nCoordinate with external/internal auditors and ensure timely closure of audit findings.
  • nProvide expert advice on cGxP regulations and guidelines.
  • nPrepare, review, and implement SOPs.
  • nCarry out internal quality audits of R&D lab and maintain Good Laboratory practices.
  • nReview and approval of risk assessments for commercial product support.
  • nRisk management, human factor, accelerated aging study, pFMEA, distribution study, sterilization assurance, etc. documents review.
  • nMonitor and evaluate the performance of process and analytical methods to identify any issues or deviations.
  • nCollaborate with other departments to ensure that all methods and procedures are compendial compliant.
  • nRepresent subject matter expertise in the areas of process and Analytical (Validation, Verification, and Transfer) as a Quality SME internally and externally as needed.
  • nCompliance verification through GEMBA walks.
  • nHandling of SNCs (Supplier Notification of change).
  • nReview and approval of Packaging development documents and data along with procedures.
  • nReview and approval of registration and commercial stability data along with trend analysis.

nRequirements:

  • nMaster or Bachelor's degree in Life Sciences, Pharmaceutical Sciences, or a related field.
  • nAt least 8-15 years of experience in Quality Assurance or related field.
  • nIn-depth knowledge and understanding of cGxP regulations and guidelines.
  • nExcellent communication and interpersonal skills.
  • nStrong technical knowledge, investigational and problem-solving skills.
  • nAbility to work in a team environment.
  • nProficient in Microsoft Office and other quality management systems.
  • nProficiency in Microsoft Office and TrackWise8.
  • nContinual system improvement and cGxP mindset

nReasonable Accommodations
n
nBaxter 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.

nRecruitment Fraud Notice
n
nBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

n148448

More Info

Industry:Other

Function:Pharmaceutical

Job Type:Permanent Job

Skills Required

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Date Posted: 13/11/2024

Job ID: 100189133

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