This is where you save and sustain lives

At 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.

Baxter'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.

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

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Essential Duties and Responsibilities 

1.    Responsible for batch manufacturing records (BMR) review for finished product release

2.    Responsible for timely product release monitoring

3.    Responsible for product hold monitoring for product release

4.    Responsible for Good Documentation Practices (GDP) issues on BMR trending and reporting

5.    Responsible for Product Quality Review and preparation of Annual Product Quality Review

6.    Responsible for preparation and release of Finished Product Certificate of Analysis (COA)

7.    Responsible for CWR process, review and monitoring

8.    Responsible for scorecard preparation on First Pass Quality (FPQ) and Product Release

9.    Responsible for initiation of Supplier Corrective Action Report (SCAR) in TW7

10.  Support Internal Quality Audit Program

11.  Back up to preparation of manual work order and rework order (JDE)

12.  Back up to preparation of critical systems monitoring for finished product release

13.  Support supplier (IPSO) initiation and tracking of ICAR (IPSO Corrective Action Report)

14.  Support supplier rating preparations and report

15.  Support supplier maintenance, re-evaluation, audits and decommissioning

16.  Support completion of RAM (Risk Mitigation) records as per request

17.  Support label (die and artwork) preparation and approval

18.  Support plant quality risk management

19.  Responsible for GMP/GDP training for plant employees and contractual

20.  Ensure update of EMS visual boards

21.  Support facility compliance with Baxter Canlubang quality standards, local regulatory and GMP requirements (PIC/S)

22.  Identified Lead Auditor for Internal Quality Audit (IQA) program at the plant

23.  Support EMS and Admin activities such as 6S, MUDA elimination, Kaizen projects, ESP, VIP, tier meetings, etc.

24.  Comply with EHS policies and participate in EHS programs

25.  Support as back up to roles of Sr. QA Analyst and QA Analysts assigned at QA Systems;

Qualifications

1. Licensed Pharmacist;

2. With sufficient background in current Good Manufacturing Practice;

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to [email protected] and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter 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.