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Process Transfer - Supervisor

Job Title: Process Transfer - Supervisor
Contract Type: Permanent
Location: Manchester, Greater Manchester
Industry:
Salary: Competitive
Start Date: ASAP
Reference: J893557_1513948301
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Job Published: December 22, 2017 13:11

Job Description

Role: Process Transfer Supervisor - Medical Device / ISO 13485

Location: Manchester

Salary: Highly Competitive

Russell Taylor Group has a fantastic opportunity for a Process Transfer - Supervisor within a Global Medical Device / ISO 13485 Company based in the area of Manchester. You will have an excellent knowledge of GMP and highly regulated environments and experience working within a manufacturing environment to the highest of standards. You will be managing the lean process as well as training mentoring staff. Great opportunity to join a Global Medical Device company.

Role:

  • Responsible for launched / approved products, operating processes and the creation and transfer of manufacturing processes within the R&D / Manufacturing and Site to Site transfers of on-market products.
  • To develop LEAN processes by removal of waste and continuous improvement of existing processes.
  • To develop news processes, transfer to manufacturing and continuous improvement of existing processes.
  • Provide internal departments with support in relation to process improvement.
  • To support and complete process validation and assist in the training of Manufacturing Staff during the validation cycle.
  • You will direct and sub-ordinate to complete assignment using established guidelines, procedures and policies.
  • Monitor all daily / weekly and monthly operations of the Process Transfer Department.

Person:

  • Ideally have a BA / BS with 4-8 years experience or MS with 1-2 years experience desired.
  • Must have a working knowledge of experimental design.
  • Advanced knowledge of GMP / highly regulated environments.
  • Must be trained or had training within Blood Borne Pathogen.
  • Technical Skills, report writing and communication skills.
  • Work well on your own as well as within a team.
  • Natural problem solver in respect of Process / Validation / Continuous Improvement.
  • Supervisory / Management experience

Keywords: Process Transfer, validation, continuous improvement, GMP, R&D, manufacturing, lean, six-sigma, 13485.