Quality Consultant in Camberley

Location: Camberley
Salary: Hidden
Recruiter: SRG
Job Hours: Full-time

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  • Title: Quality Consultant
  • Contract Length: 12 months.
  • Location: Hybrid - Camberly site
  • Contract - 12 months
  • SRG are working with a pharmaceutical company looking for a Quality Consultant to join their Camberly team.

    Job Purpose:

  • To ensure compliant and efficient execution of a quality project across the UK and Ireland organizations.
  • Gap assessment of the QMS for a new entity
  • Project planning to ensure effective and compliant integration of current QMS with to be QMS of the established entity.
  • Ownership of the project planning and execution.
  • Implementation of project plan to ensure effective QMS in new entity.
  • Creation of Quality agreements and contracts

  • Major Accountabilities:

  • Execute elements of the quality management system to support GMDP activities at the Country Organisation and, where required/experienced, support ownership of a quality process or system - this includes understanding and assessment of SOPs, documents, records and metrics related to the systems. Support evaluation any issues/gaps and improvement implementation.
  • To ensure compliant and efficient execution of a quality project across the UK and Ireland organizations.
  • Gap assessment of the QMS for a new entity
  • Project planning to ensure effective and compliant integration of current QMS with to be QMS of the established entity.
  • Ownership of the project planning and execution.
  • Implementation of project plan to ensure effective QMS in new entity.
  • Creation of Quality agreements and contracts
  • Support in audits/ inspections/ self-inspection programme when required.
  • Operate the Country Organisation quality activities following SOP's and using documentation/IT system confidently as required
  • Gain knowledge of IT platforms/applications required to operate tasks in those quality systems
  • Completion of training in compliance
  • Deliver on time for individual actions or commitments - or reschedule appropriately as needed. This includes own training commitments and also actions to support others (e.g. reviews and approvals)


  • Education & Qualifications:

    Life science degree level

    Experience:
    * 10 years' experience in the pharmaceutical industry, GxP knowledge
    * Good level of skills in the use of computer based systems and applications

    Skills & Knowledge:

    Strategic/Transitional Skills

  • Demonstrate Continuous Learninng
  • Interpersonal relationships and collaboration
  • Operational Excellence - constructively challenge inadequate, inefficient or unnecessary processes and makes suggestions for improvements.
  • Being Resilient, Motivated, Managing multiple priorities.
  • Organisation skills - self-directed and able to flex to meet peaks in workload. Stays focused on tasks despite disruptions or obstacles

  • Functional Quality Knowledge/Skills

  • Quality System Management
  • Understand Regulatory Environment - Knowledge of GMDP and other regulatory requirements relevant for country organisation
  • Quality Governance/Compliance - Support preparation for audits and inspections.
  • Project management experience for Quality

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