Christopher Stafford

Christopher Stafford Email and Phone Number

Quality consultant supporting the Medical Device industry @
Christopher Stafford's Location
Mold, Wales, United Kingdom, United Kingdom
About Christopher Stafford

In excess of 30 years experience in the medical device and diagnostics field. Results-focused with a strong commitment to professionalism and quality. Certified Johnson & Johnson Six Sigma / Process Excellence Black Belt (2007). Excellent problem solving capabilities and the ability to contribute original ideas. Substantial experience in the validation of equipment and processes. Excellent oral and written presentation skills. Member of the Royal Society of Chemistry (Charted Chemist) (1991).

Christopher Stafford's Current Company Details
QualOpus GSE Ltd

Qualopus Gse Ltd

Quality consultant supporting the Medical Device industry
Christopher Stafford Work Experience Details
  • Qualopus Gse Ltd
    Director
    Qualopus Gse Ltd Jun 2019 - Present
    Mold, Wales, United Kingdom
  • Purple Surgical
    Quality Manager
    Purple Surgical Nov 2018 - Jun 2019
    Taunton, United Kingdom
  • Inside Biometrics International Ltd
    Quality Manager
    Inside Biometrics International Ltd Feb 2015 - Nov 2018
    Inverness, United Kingdom
  • Lifescan
    Senior Design Quality Engineer
    Lifescan Sep 2014 - Jan 2015
    Inverness
    Project Representative for Design Quality input into current development project. Responsible for Quality review and approval of all project documentation including verification and validation activities. Accountable for project risk management activities.
  • Integra Lifesciences
    Qa Capa Coordinator
    Integra Lifesciences Jun 2014 - Aug 2014
    Andover
    Responsible for all CAPA activities on-site, including tracking and reporting of metrics. Coordinated and facilitated CAPA process. Drove open CAPA’s to closure.
  • Lifescan
    Validation And Verification Engineer
    Lifescan Sep 2011 - Mar 2014
    Inverness, United Kingdom
    Responsible for validation and verification activities and the assessment of testing methodologies.
  • Lifescan
    Innovation Processes & Systems Specialist
    Lifescan Jun 2010 - Sep 2011
    Member of the team responsible for the maintenance of New Product Development Process, Design Controls, and Requirements Management activities.
  • Lifescan
    Value Stream Engineer
    Lifescan 2007 - Jun 2010
    Responsible for leading process validation activities.
  • Lifescan
    Project Scientist
    Lifescan 2003 - 2007
    Inverness, United Kingdom
    Responsible for process improvement activities and their validation.
  • Lifescan
    Quality Engineer
    Lifescan 2002 - 2003
    Inverness, United Kingdom
    Responsible for continuous improvement projects.
  • Lifescan
    Supplier Development Manager
    Lifescan 2001 - 2002
    Inverness, United Kingdom
    Responsible for the implementation and monitoring of key suppliers by the use of supplier assessment reports and development plans.
  • Lifescan
    Process Engineer
    Lifescan 1999 - 2001
    Inverness, United Kingdom
    Responsible for process improvement activities and their validation.
  • Ares Serono Group
    System Scientist
    Ares Serono Group 1988 - 1999
    Woking, Surrey
    Project Leader responsible for overseeing the development of a commercial instrument prototype at third-party. Established the company quality policy. Responsible for scale-up of manufacturing technology from R&D to pilot scale - reviewed and updated all SOP’s and trained new team. Responsible for production, purification and assessment of monoclonal antibodies, at both small-scale and bulk quantities. Developed new methods for protein purification.
  • Venture Technology
    Development Chemist
    Venture Technology 1985 - 1988
    Abingdon, Oxfordshire
    Developed novel lithium battery technologies for external bodies. Technical resource on multi-disciplinary team developing fully-automated commercial manufacturing lithium battery production equipment for UK and overseas markets.

Christopher Stafford Skills

Project Management Lean Enterprise Implementation Corrective Action Preventive Action Validation Process Excellence Mentoring Coaching Six Sigma Process Improvement V&v Continuous Improvement Medical Devices Manufacturing R&d Design Control Product Development Iso 13485 Capa Fda Quality Assurance Quality System Corrective And Preventive Action Iso 14971

Christopher Stafford Education Details

  • University Of Southampton
    University Of Southampton
    Electrochemical Science
  • University Of London
    University Of London
    Chemistry

Frequently Asked Questions about Christopher Stafford

What company does Christopher Stafford work for?

Christopher Stafford works for Qualopus Gse Ltd

What is Christopher Stafford's role at the current company?

Christopher Stafford's current role is Quality consultant supporting the Medical Device industry.

What schools did Christopher Stafford attend?

Christopher Stafford attended University Of Southampton, University Of London.

What skills is Christopher Stafford known for?

Christopher Stafford has skills like Project Management, Lean Enterprise Implementation, Corrective Action Preventive Action, Validation, Process Excellence, Mentoring, Coaching, Six Sigma, Process Improvement, V&v, Continuous Improvement, Medical Devices.

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