Assoc. Quality - IPQA: Elevate Your Career in Pharmaceutical Excellence
Be Part of a Mission That Saves Lives
At Baxter, every role contributes to a mission that transforms lives. We are dedicated to advancing healthcare through groundbreaking innovations, ensuring that our products and therapies reach millions of patients worldwide. Our commitment extends beyond manufacturing—we create an environment where professionals thrive, collaborate, and make a meaningful impact.
If you are passionate about quality assurance and want to be part of a dynamic team, this role in In-Process Quality Assurance (IPQA) is your opportunity to grow and excel.
Key Responsibilities
Ensuring Compliance & Quality Control
- Conduct line clearance at various stages of manufacturing and packaging in alignment with Batch Manufacturing Records (BMR).
- Verify raw materials and packaging materials, ensuring accuracy in quantity and compliance with approved batch records.
- Perform in-process quality checks, sampling, and periodic verification to uphold product integrity.
- Maintain and verify electronic records, audit trails, and equipment printouts to ensure compliance.
- Ensure proper handling, storage, and disposal of documents as per regulatory guidelines.
- Adhere to Good Documentation Practices (GDP) and maintain data integrity throughout the process.
Process Improvement & Risk Management
- Identify and escalate non-conformities while supporting Corrective and Preventive Actions (CAPA).
- Assist in investigations related to product complaints, deviations, and out-of-specification (OOS) incidents.
- Execute change control processes (DCR, CCM) and ensure timely implementation.
- Participate in continuous process verification (CPV) and analyze critical process parameters (CPPs) to maintain quality standards.
System & Equipment Management
- Oversee admin logins and access control for relevant equipment and ensure periodic verifications.
- Initiate batch numbers in BaxLIMS and validate manufacturing and expiry details.
- Approve and track preventive maintenance activities in MAXIMO, ensuring risk assessments are conducted.
- Perform impact assessments for breakdown maintenance and oversee necessary corrective actions.
Collaboration & Shift Coordination
- Maintain shift-to-shift handovers and document key updates in the logbook.
- Communicate failures or deviations promptly to supervisors for resolution.
- Participate in building inspections with the admin team to ensure facility compliance.
- Support training, mentoring, and adherence to safety and quality standards.
Why Join Baxter?
- Work at the forefront of pharmaceutical quality assurance, ensuring product safety and efficacy.
- Be part of a collaborative and innovation-driven environment that values your expertise.
- Enjoy continuous learning opportunities and career growth in a global healthcare company.
How to Apply
If you are ready to contribute to a mission that saves and sustains lives, apply now and be part of Baxter’s commitment to quality and patient safety.