QA - Drug Development & Preclinical Studies - Wirral, United Kingdom - Cpl Life Sciences

Cpl Life Sciences

Verified Company

Wirral, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Quality Assurance

Drug Development and Preclinical Studies / QA - Dev & Preclinical

12 Month Contract

£19.23 per hour, 35 hours per week

Moreton, Merseyside - 50/50 Remote/On-site

Key Responsibilities
Project Manage/support the External QP release process.
Co-ordinate/align on all required documentation.
Triage/answer any QP related queries.
Liaise with Trials Supplies Management (TSM), Trial Managers (TM) and Regulatory Affairs.
Identify dependencies, evaluate risks, and communicate status to appropriate levels of management and stakeholders across the business.

Ensure project deliverables and schedules are met, adhere to established standards, which are managed in alignment with client Project Management best practices across their assigned projects.

Proactively remove obstacles to drive assigned project's momentum and progress
Plan and engage necessary resources across the enterprise to ensure successful completion of assigned projects.
Support the PDQ function at Moreton to ensure timely release of Investigational Medicinal Products (IMPs).

Qualifications & Experience
Degree qualified or equivalent experience required.
Project Management experience is essential.
Previous Pharmaceutical Quality experience is desired/preferred.
Demonstrated experience leading initiatives related to continuous improvement and/or implementation of new ways of working.
Demonstrated ability to build and leverage relationships through diplomacy with a broader focus?within the Function.
Experienced in process improvement.
Ability to recognize the potential impact on internal/external challenges on the future state success.
Good knowledge/experience in computer systems (MS, excel, word, etc.).
Ability to co-ordinate/lead meetings.