Packaging and Labelling Supervisor

Blackfield Associates; Wirral; On-site; GBP 40,000 - 65,000; Full time

Job summary

An established industry player is seeking a Packaging & Labelling Supervisor to lead a skilled team in a high-impact pharmaceutical environment. This pivotal role involves overseeing the packaging of clinical trial supplies within a state-of-the-art cGMP production facility. You'll ensure quality and compliance while driving continuous improvement and supporting cross-functional collaboration. If you are ready to make a significant impact and thrive in a dynamic setting, this opportunity is perfect for you.

Qualifications

• Proven leadership in a production or packaging setting.
• In-depth knowledge of cGMPs and regulatory requirements.

Responsibilities

• Lead and supervise a team in clinical supplies packaging & labelling.
• Ensure compliance with cGMPs, SOPs, and health & safety guidelines.

Skills

Leadership in production

Knowledge of cGMPs

Communication skills

Scheduling abilities

Multitasking abilities

Education

Bachelor's degree in Science

Bachelor's degree in Mechanical Engineering

Tools

SAP

Veeva

MS Office

Job description

3 weeks ago Be among the first 25 applicants

Direct message the job poster from Blackfield Associates

Packaging and Labelling Supervisor

Are you ready to lead a skilled team in a high-impact pharmaceutical environment? A reputable client of ours is looking for a Packaging & Labelling Supervisor to oversee the packaging of their clinical trial supplies in a state-of-the-art cGMP production facility.

This is your chance to step into a pivotal leadership role where you’ll ensure quality, compliance, and efficiency every step of the way.

Responsibilities

What You’ll Be Doing:

• Lead and supervise a team in clinical supplies packaging & labelling
• Oversee daily operations, schedules, and resources for production
• Ensure strict compliance with cGMPs, SOPs, and health & safety guidelines
• Maintain production accuracy through systems like SAP
• Drive continuous improvement and support cross-functional collaboration
• Conduct staff training and support technical documentation efforts
• Investigate and resolve process deviations with corrective actions

Requirements

Requirements:

• Proven leadership in a production or packaging setting
• In-depth knowledge of cGMPs and global regulatory requirements (MHRA, FDA, EU CTR)
• Experience in clinical trial supplies or pharmaceutical manufacturing
• Bachelor’s degree in Science or Mechanical Engineering (required)
• Strong communication, scheduling, and multitasking abilities
• Proficiency with tools like SAP, Veeva, MS Office

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Production

• Industries

  Pharmaceutical Manufacturing

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