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Production Support

Req #: 180005L7_en
Location: Dublin, L IE
Job Category: Manufacturing
Date Posted: 3/21/2018 10:28:53 AM
Baxter International

Description

About Baxter
Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
 
 
A Career That Matters
Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.
 
The Role
As a Production Specialist, you will be responsible for supporting the compounding plant in improving the standard of our quality management systems within the Sandford facility with respect to compounding, quality and EHS.
 
Responsibilities
 
  • Assist production team in ensuring that an effective Quality System is in place and is in line with HPRA and Baxter Healthcare standards.
  • Play a leading role in NCR & CAPA management within the Baxter Sandyford Site.
  • Coordinate investigations using appropriate methodology to identify the root cause and implement effective actions to ensure non-reoccurrence.
  • Act as a liaison between production and quality personnel to resolve manufacturing, quality and technical issues and to facilitate proactive quality improvements of the manufacturing processes.
  • Ensure that any deviations are addressed effectively and promptly and in accordance with agreed standards.
  • Support process improvement programs with in the Baxter Sandyford Site.
  • Compliance to Good Manufacturing Practices (GMP) or Good Distribution Practices (GDP) as applicable.

Qualifications

  • Diploma in a science/healthcare Technology.
  • Strong and relevant experience in manufacturing.
  • Good understanding of Start to End manufacture process and supporting activities.
  • GMP manufacturing environment experience is necessary.
  • Knowledge of GMP’s in a sterile manufacturing environment.
 
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, colour, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.
 
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