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Production Supervisor

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Baxter

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Location:
United Kingdom , Oxford

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Category:
Manufacturing

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

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

Job Responsibility:

  • Leading, driving and managing multiple manufacturing teams responsible for compounding any aseptically compounded product
  • Working 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
  • Driving manufacturing activities to ensure that they are aligned to the commercial business requirements
  • Reporting on daily production plan adherence and loss analysis, and other required Unit metrics
  • Developing and leading a collaborative, diverse and inclusive environment for all staff
  • Supporting Training completion, EHS activities and a culture of equipment optimisation and process Continuous Improvement
  • Being a continuous visible presence in the manufacturing areas leading by example and setting high standards of compliance to GMP and Company policies
  • Providing cover for the Unit / Operations manager when required including Leadership Team meetings
  • Monitoring, controlling, and adjusting manufacturing process as required to meet output requirements
  • Leading and inspiring a team of Team Leaders and Deputy Team Leaders, and through them management of the compounding manufacturing team
  • Effectively managing absence levels and annual leave in line with company policies
  • Developing, monitoring, and reporting on key performance indicators for unit
  • Having a working knowledge of equipment operation and optimising the efficiency of said equipment and resources in the manufacturing area
  • Ensuring compliance with all GMP, Regulatory & Corporate requirements and actively participating in internal, Corporate and Regulatory audits
  • Ensuring compliance to the UK Compounding EHS Management system with a focus on incorporation of safe practices for the area
  • Maintaining, updating or creation of Unit SOP’s
  • Recruiting headcount to ensure effective execution of workload targets
  • Ensuring competence and development within team and maintaining personal level of CPD
  • Collaborating and sharing best practises to ensure timely completion of deviation and complaint investigations to identify true root cause and the elimination of future re-occurrences
  • Maintaining and driving a program of opportunities to drive continuous improvement, collaborate on decisions and deliver the results whilst ensuring an appropriate level of compliance
  • Driving change control activities to timely completion

Requirements:

  • 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 we offer:
  • Competitive total compensation package
  • Professional development opportunities
  • High importance placed on work life balance

Additional Information:

Job Posted:
March 19, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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