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Deputy Lab Manager

£Competitive | East Riding |  Clinical Research, Clinical CRO |  Permanent  | Ref:890144

The Role

Deputy Lab Manager - Consumer Health Company - Hull

*Interviews & onboarding remotely*


The Company

A very interesting role within a reputable consumer health company who have years' experience in bringing healthcare goods and products to the market.

  • People focussed company, they continually invest for their staff
  • Over 80% of the staff are proud to work here
  • One of the top FMCG employers
  • Excellent support and progression to ensure you succeed within the business


The Role

Reporting directly to the R&D Health Analytical Sciences Manager, the purpose of this role is to support the Lab Manager in the leadership and day-to-day management of the R&D Analytical Sciences Laboratories to ensure it meets the requirements of the cGMP guidelines and global regulatory requirements for pharmaceutical development including FDA, MHRA and EMA.

  • Laboratory day-to-day management (housekeeping, fault resolution, resource planning and expert guidance)
  • Provision of defined procedures, review, approval and monitoring of analytical method development and validation
  • Identifying functional training needs and the solutions and budgets to mitigate these needs, and building appropriate technical competency levels across the Category teams
  • Responsible for the effective coordination and installation of all new analytical technology
  • Identify and establish alternative ways of working and drive a culture of continuous improvement
  • Via leadership of the compliance team maintain audit readiness of the analytical labs through a defined programme of audits and housekeeping initiatives



  • A minimum of a bachelor's or master's degree (or equivalent) in a relevant science discipline
  • The ability to effectively influence and resolve priority conflicts of people not directly reporting to them
  • A working knowledge or accreditation in lean-six-sigma principles would be advantageous
  • Theoretical and practical knowledge of all mainstream analytical technologies and equipment and their validation
  • Practical knowledge of cGMP and associated industry guidelines
  • Practical knowledge of UK Health and Safety Regulations and their implementation in an analytical laboratory
  • Flexibility and a positive attitude to changes in priority at short notice


What should you do next?

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



Claire Craig

Which team and area do you work/specialise in?

Clinical Operations as part of the Drug Development team

What are some of the typical roles you cover?

  • Senior and Clinical Research Associates
  • Clinical Trial Administrators
  • Research Nurses/Advisors
  • Patient Recruitment Roles
  • Study Start up roles

What are the hot issues in your sector currently?

Brexit, unsure if regulations etc will change within Clinical Trials

What’s makes you #DistinctlyDifferent?

Building relationships with my clients and candidates that are different to what they have had before. Consistent contact throughout the entire process. It works well and shows in results.


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