Specialist, Validation

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

Sandyford and Deansgrange sites require this critical position for maintaining validated state of all manufacturing, storage & transport areas and equipment according to the applicable regulatory requirements.

Job Description

Essential Duties and Responsibilities:

Spearhead qualifying and validating new equipment and processes timely. Join Baxter Healthcare in Dublin as a Validation Specialist, playing a crucial role in maintaining top-tier operational standards!

Execution of Validation activities

We adhere strictly to regulatory, cGMP, Standard Operating Procedures, Policies, and any other rules defined by the Company. Ensuring the site Validation Master Plan (sVMP) is maintained and activities listed within are actioned in a timely manner is crucial. Additionally, we manage Deviation and Non-Conformance, including Root Cause Analysis (RCA) and Corrective and Preventive Actions (CA/PA).

Change Control Management

Discovering opportunities and presenting justified solutions for encouraged improvements is vital. You'll assist CPI and CQI programs by training teams. Building indicators and targets for teams and management is part of your duties. Engaging in Baxter projects, audits, and keeping validation documents in an "audit-ready" state is encouraged.

Qualifications

You should possess a Basic Science, Engineering, or Pharmacy qualification, and demonstrate knowledge and understanding of the requirements of the position.

Project Management experience

Hands-on experience in pharmaceutical aseptic production is required.

Experience in 6-Sigma and Lean Manufacturing

You should exhibit skills in problem-solving, system development, application of technological and business tools, and the use of IT systems.

Logical, practical-minded with a hands-on approach

Candidates must demonstrate creativity, analytical skills, and innovation in their approach!.

Self-motivated and able to motivate others

You should show good judgement to achieve a balance between cost-benefit, quality, and safety.

Able to communicate effectively, written and oral

The ideal candidate will demonstrate proficiency in managing resources and time efficiently, coupled with clear and effective communication skills in both written and verbal formats.

“What are some of our benefits of working for Baxter?

• Competitive total compensation package
• Professional development opportunities
• High importance placed on work life balance
• Pension
• Health Insurance
• Life Assurance
• Competitive Salary

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Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter 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.

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