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QA Manager - Pharma - Licensed Manufacturing Products Sterile

Vacancy Title: QA Manager - Pharma - Licensed Manufacturing Products Sterile
Contract Type: Permanent
Location: Wembley, London
Industry:
Salary: £50000 - £60000 per annum + Benefits
Start Date: ASAP
REF: J907792_1618561478
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Vacancy Published: 30 days ago

Vacancy Description

Role: QA Manager - Pharmaceutical - Licensed Manufacturing Products

Salary: Highly Competitive

Location: Wembley, London, UK

Russell Taylor Group has a fantastic opportunity for a QA Manger with licenced manufacturing pharmaceutical products and sterile experience to join a national pharmaceutical company near to Wembley. You will be responsible for managing quality systems, processes, and procedures to assure product safety and quality by driving business alignment to correct industry requirements and business objectives by managing quality system design, controls, and continuous improvement.

Role:

  • Lead the site and CMO in GXP compliance
  • Manage day-to-day activities of QA staff
  • To manage and approve OOS/OOT process for site
  • To review, collate data and write PQRs/SQRs for Pharmaceutical products
  • To review batches and support QP product release
  • To manage the site equipment validation and calibration annual planner
  • To manage quality systems, processes and procedures to assure product quality and safety
  • To engage strong intradepartmental and cross-functional/organizational relationships to drive Quality System Requirements (QSRs)
  • Own the development and maintenance of policies and procedures for departmental functions
  • Influence site compliance to Quality policy, Quality Management System procedures and guidelines
  • Lead in compliance to internal and external regulations
  • Lead quality system metrics such as Corrective and Preventive Action, training metrics, completion and complaint resolution metrics
  • Define and perform audit of internal systems and external suppliers and manufacturers
  • Inform appropriate internal departments on audit results and work with the necessary staff to achieve GXP compliance
  • Leading regulatory authority inspections
  • Develop and maintain GxP standard operating procedures in accordance with regulatory and company requirements
  • Update key performance indicators/metrics in a timely manner

Person:

    • Degree in a relevant scientific discipline
    • Minimum 10 yrs hands on Pharmaceutical Quality Experience preferably within Licensed Manufacturing
    • Extensive Management Experience
    • Sterile products experience
    • Experience working with the integration of new products and manufacturing processes
    • Management of up to 10 staff (not essential)
    • If you are a QA Manager with a QP licence we would also like you to apply.

Keywords; Pharma, Quality, QMS, licensed, sterile, manufacturing,

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