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Quality Assurance

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Quality Assurance

Quality Assurance is a vital area of expertise in all Pharmaceutical, Medical Device or BioTech organisations to ensure customer safety and to protect their products. An organisations Quality Management System will link all parts of the product development process and our team here at Adaptive Life Science are able to provide professionals for all phases from Senior QA Managers to Validation experts (Equipment Validation, System Validation and Process Validation) to QP’s and Quality Control experts.


We specialise in finding professionals both on a permanent basis and also those who can operate under pressure as an interim consultant for a set period of time. We tailor the search within our network to source the right candidate with the specific experience and skill sets that our clients require to ensure compliance with Quality and Safety regulations.


We work across the Pharmaceutical, Medical Device and Biotech sectors, allowing our clients to complete their projects safely in the knowledge that the correct quality processes are adhered to ensuring a safe passage for their product from initial R&D phase right through to the release phase and beyond.

Roles recruited for:

  • QA Management
  • Validation Experts
  • Quality Management System (QMS)
  • Quality Control Officer
  • Global Head of Quality
  • Qualified Person (QP)
  • Team and Department management
  • Quality Officer/Engineer


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    QA Manager

    As a Quality Assurance Manager, you will be a key contributor and supporter of the companies Quality Management System, it will be run to ISO standards of which you will know the impacts of not following.


    Be it to ISO9001 or ISO13485 standards you will champion the need to follow such processes to ensure compliance and best practice.


    You may be managing the QA aspects of individual products, whole projects, functional areas or business segments but working closely with the Regulatory teams to ensure a joined-up approach to compliance for the business.

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    Validation Experts

    Be it CSV, Process, Quality or Equipment the many areas of Validation exist within Pharmaceuticals and the Medical Device industries forming a crucial area of the process to ensure safe and profitable products go out the production door.


    deally from an engineering background you will have developed a niche specialism within Validation offering an expert service on either a permanent or interim basis working closely with the Quality teams to drive high standards.

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    Head of Quality Management

    Coming from an engineering background you will have focused your career onto Quality Management.


    You will be experienced in maintaining and strategically developing a QMS that meets the requirements of your business and ISO 9001/13485. You will have built and established a culture of continuous, systematic improvement of quality to increase competitiveness.


    You will have a team reporting to you of Quality personnel that may also include Regulatory Affairs professionals.

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    Qualified Person

    Having graduated with a natural science degree be it in Pharmacy, Chemistry or another similar subject you will have worked your way through the Quality career into the position of ‘Qualified Person’. You will ensure product flow and the team meets all product quality and compliance requirements to enable disposition for each batch of drugs.


    This requires the management of a robust Quality Management System to support a flexible, collaborate, multi-skilled teamwork environment. providing quality support, guidance and expertise on all Quality Assurance and cGMP compliance aspects to ensure the success of transference will be done.