Production Supervisor (Night Shift)

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. 

Reporting to the Unit or Operations Manager, The Production Supervisor will be responsible for leading, driving and managing multiple manufacturing teams responsible for compounding any aseptically compounded product supplying the UK and Ireland market.

They will work within any grade A to D cleanroom and be fully conversant with the quality and working requirements of these areas and the equipment used within them, ensuring compliance with the manufacturing license and quality systems.

They will drive manufacturing activities to ensure that they are aligned to the commercial business requirements by close collaboration with the associated teams of planning, production, engineering, quality and logistics.

The Production Supervisor is responsible for reporting on daily production plan adherence and loss analysis, and other required Unit metrics.

They must develop and lead a collaborative, diverse and inclusive environment for all staff and play an actively involved role in supporting Training completion, EHS activities and a culture of equipment optimisation and process Continuous Improvement

The Night Shift runs Sunday - Thursday between the hours of 10pm and 6am.

• Being a continuous visible presence in the manufacturing areas leading by example and setting high standards of compliance to GMP and Company policies.

Collaborate and share best practises to ensure timely completion of deviation and complaint investigations to identify true root cause and the elimination of future re-occurrences.

Maintain and drive a program of opportunities to drive continuous improvement, collaborate on decisions and deliver the results whilst ensuring an appropriate level of compliance.

Drive change control activities to timely completion.

Experience / Skills

• Proven experience in direct line-management
• Proven experience in end-to-end manufacturing process organisation
• Proven experience in lean, investigational, and optimising projects
• Pharmaceutical, process, industrial, chemical manufacturing, or related industry experience
• English minimum equivalent to RQF Grade 2, EQF Grade 3 or SCQF Grade 5
• Degree in life science, engineering (pharmaceutical, process, industrial, chemical), or equivalent
• Cleanroom experience
  
  

What are some of the benefits of working at Baxter?

• Competitive total compensation package
• Professional development opportunities

High importance placed on work life balance

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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

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