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Quality Control Validation Manager

Hobson Prior Ltd
Posted 3 days ago, valid for 7 days
Location

London, Greater London SW1A2DX, England

Salary

£55,000 - £66,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • Hobson Prior is seeking a Quality Control Validation Manager for a pharmaceutical company in London, UK.
  • The role requires a degree in Human Health or Sciences and relevant experience in a validation role within the pharmaceutical industry, with a focus on developing and validating analytical test methods for gene therapy products.
  • Candidates must have the ability to manage a team, deliver projects on time, and ensure compliance with regulatory standards, including GMP and FDA regulations.
  • The position offers a competitive salary, although the exact figure is not specified in the job description.
  • Interested candidates should apply by submitting their CV or contacting a life sciences recruitment specialist for further details.

Hobson Prior is working alongside a pharmaceutical company seeking a Quality Control Validation Manager to join the team in London, UK. This role will focus on developing and validating analytical test methods for gene therapy products, managing projects, and ensuring compliance with regulatory standards.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Develop and validate new and existing test methods for gene therapy products.
  • Manage the lifecycle of analytical tests, equipment, and materials.
  • Create and maintain documentation to support analytical activities.
  • Ensure all methods are validated and compliant with regulatory standards.
  • Oversee external testing activities to meet GMP requirements.
  • Communicate effectively with stakeholders and maintain updated information.
  • Train staff on new technologies and methods.
  • Regularly assess and ensure the proper application of analytical methods.
  • Support training and quality management system activities.
  • Ensure compliance with quality, safety, and environmental procedures.
  • Track and achieve key performance indicators and objectives.
  • Ensure all work complies with GMP, Data Integrity, and Good Documentation Practice (GDP).

Key Skills and Requirements:

  • Degree in Human Health or Sciences or equivalent relevant experience.
  • Experience in a validation role within the pharmaceutical or regulated industry.
  • Proven ability to manage a team and deliver projects on time.
  • Independent, goal-oriented, and efficient in a fast-paced environment.
  • Ability to manage multiple projects simultaneously.
  • Knowledge of EU and FDA regulations, GMP/GLC/GCP, Lean Manufacturing, Six-Sigma, etc.
  • Proficiency in Microsoft Office software (Word, Excel, PowerPoint).
  • Willingness to travel between sites.

For more information, please contact Frankie Cunningham.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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