Process Quality Excellence Specialist 14257 3
Process Quality Excellence Specialist 14257 3
Posted on :
09-01-2025
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1 Vacancy
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Job Description
CK Group are recruiting for a Process Quality Excellence Specialist to join a global pharmaceutical company, based in Slough on a contract basis initially for 12 months. This is a hybrid role with 2 times a week required on site.
Salary:
20.03 (PAYE) per hour or 27.27 per hour (Umbrella)
Process Quality Excellence Specialist Role:
Strong pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting.
In depth experience of GCP, including hands on experience in global GCP audits and/or inspections
FDA/EMA inspection readiness experience is essential.
Company:
Our client is a is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location:
This role is based at our client s site in Slough.
Apply:
For more information, or to apply for this Process Quality Excellence Specialist role please contact the Key Accounts Team onor email Please quote reference 112 877.
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Salary:
20.03 (PAYE) per hour or 27.27 per hour (Umbrella)
Process Quality Excellence Specialist Role:
- Support the HPQE in GCSO quality and compliance infrastructure development; assist with creation/revision of appropriate quality and compliance policies, Standard Operating Procedures (SOPs), processes, and best practices as needed.
- Work in collaboration with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for Pharmaceutical for Human Use (ICH) GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness.
- Participate in Audit and Inspection planning with Global Quality.
- In liaison with the Clinical Project Managers, for managing Study Specific Training activities within the Learning Management System (LMS). This includes creating and maintaining study training matrices, developing relevant curriculums and courses, activating and deactivating study training for study team members, and providing support to GCSO stakeholders as needed.Represent or ensure GCSO representation and preparation during audits/inspections.
- Attend improvement initiatives to improve quality and compliance processes and effectiveness in collaboration with stakeholders
Strong pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting.
In depth experience of GCP, including hands on experience in global GCP audits and/or inspections
FDA/EMA inspection readiness experience is essential.
Company:
Our client is a is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location:
This role is based at our client s site in Slough.
Apply:
For more information, or to apply for this Process Quality Excellence Specialist role please contact the Key Accounts Team onor email Please quote reference 112 877.
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Employment Type
4
Company Industry
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