Quality Engineer β€” GMP-Driven Pharma Manufacturing & CI in Clitheroe

Quality Engineer β€” GMP-Driven Pharma Manufacturing & CI in Clitheroe

Clitheroe Full-Time 29700 - 36300 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead projects in pharma manufacturing, focusing on quality and continuous improvement.
  • Company: Kindeva Drug Delivery, a leader in drug delivery technology.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and compliance.
  • Why this job: Make a real impact in the pharma industry while ensuring product quality and safety.
  • Qualifications: Experience in manufacturing technology and strong analytical skills.

The predicted salary is between 29700 - 36300 Β£ per year.

Kindeva Drug Delivery is seeking a Manufacturing Technology professional to support/lead projects across the full production lifecycle of MDI valves and cans. You will drive investigations, validation activities, and continuous improvement initiatives within a GMP environment, liaising with cross-functional teams to deliver high quality, compliant solutions.

The role emphasizes data analysis, documentation, and adherence to regulatory standards, with a commitment to safety and continuous improvement.

Quality Engineer β€” GMP-Driven Pharma Manufacturing & CI in Clitheroe employer: Kindeva Drug Delivery

Kindeva Drug Delivery is an exceptional employer that values innovation and collaboration, offering a dynamic work culture in Loughborough. Employees benefit from flexible hours, a competitive compensation package, and ample opportunities for professional growth within the global procurement landscape. Join us to be part of a team that is dedicated to making a meaningful impact in drug delivery solutions.

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Contact Details:

Kindeva Drug Delivery Recruitment Team

We think you need these skills to ace Quality Engineer β€” GMP-Driven Pharma Manufacturing & CI in Clitheroe

Manufacturing Technology
GMP Compliance
Project Leadership
Data Analysis
Validation Activities
Continuous Improvement
Cross-Functional Collaboration