Senior QA Advisor
Hyper Recruitment Solutions are currently looking for a Senior QA Advisor to join a leading life science company based in the Cambridgeshire area. As ... View Job
We are currently looking for a Quality Manager to join a global life science company based in the Kent area. As the Quality Manager you will be respon... View Job
Quality Manager / QP
We are currently looking for a Quality Manager / QP to join a pharmaceutical company based in the South East. As the Quality Manager / QP you will be ... View Job
The Sr. QA Manager will manage 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.
SECONDARY RESPONSIBILITIES ·Lead the site 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 ·Update key performance indicators/metrics in a timely manner ·Develop and maintain GxP standard operating procedures in accordance with regulatory and company requirements
Role holder qualifications ·Degree in scientific discipline ·Hands on pharma QA experience / management experience