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QA Manager - Pharma - Licensed Manufacturing Products Sterile job in London at Russell Taylor Group Ltd

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QA Manager - Pharma - Licensed Manufacturing Products Sterile at Russell Taylor Group Ltd

QA Manager - Pharma - Licensed Manufacturing Products Sterile

Russell Taylor Group Ltd Wembley, London Full-Time
£50,000 - £60,000 / year
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Role: QA Manager - Pharmaceutical - Licensed Manufacturing Products

Salary: Highly Competitive

Location: Wembley, London, UK

Russell Taylor Group has a fantastic opportunity for a QA Manager 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,

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k
 

Recommended Skills

Quality Management
System Procedures
Product Quality Assurance
Quality Management Systems
Corrective And Preventive Action (Capa)
Pharmaceuticals
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Job ID: 213556549

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