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- Tasks: Lead quality operations for clinical supply chains and manage project priorities.
- Company: Join a prestigious client in Wirral focused on clinical trials and supply chain excellence.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and development.
- Why this job: Make an impact in healthcare by ensuring timely delivery of clinical supplies and approvals.
- Qualifications: Project management experience is essential; pharmaceutical quality experience preferred.
- Other info: Ideal for those passionate about continuous improvement and process optimization.
The predicted salary is between 43200 - 72000 £ per year.
Quality Operations Project Manager – Clinical Supply Chain – Wirral
Prestigious Wirral based client requires an accomplished Quality Operations Project Manager with solid experience and understanding of Clinical Trials and Clinical Supply Chain management. You will support the External Manufacturing Quality team, due to the insourcing of newly acquired acquisition clinical trials. The Quality Operations Project Manager will manage the prioritizing and alignment of external Qualified Person (QP) release of clinical supplies at Contract Manufacturing Organisations (CMOs) and partner with Regulatory Affairs and Global Clinical Supply Chain to ensure on-time delivery of Health Authority approvals for release of clinical supplies (as applicable).
Essential Responsibilities:
- 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.
- Knowledge of clinical trial documentation submission and approval preferred.
- Knowledge of clinical supply chain.
Click Apply now to be considered for the Quality Operations Project Manager – Clinical Supply Chain – Wirral role.
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Quality Operations Project Manager - Wirral employer: Gibbs Hybrid
Contact Detail:
Gibbs Hybrid Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Operations Project Manager - Wirral
✨Tip Number 1
Make sure to highlight your project management experience in your conversations. This role requires strong project management skills, so be ready to discuss specific projects you've led and the outcomes.
✨Tip Number 2
Familiarize yourself with the clinical supply chain processes and any recent changes in regulations. Being knowledgeable about current trends will help you engage in meaningful discussions during interviews.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, especially those involved in quality operations and clinical trials. Building relationships can provide insights and potentially lead to referrals.
✨Tip Number 4
Prepare to discuss your experience with continuous improvement initiatives. Be ready to share examples of how you've implemented new processes or improved existing ones in previous roles.
We think you need these skills to ace Quality Operations Project Manager - Wirral
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Operations Project Manager position. Highlight key responsibilities and required skills, such as project management experience and knowledge of clinical supply chains.
Tailor Your CV: Customize your CV to reflect your relevant experience in project management and pharmaceutical quality. Use specific examples that demonstrate your ability to lead initiatives and improve processes.
Craft a Compelling Cover Letter: Write a cover letter that connects your background to the role. Emphasize your experience with clinical trials and your ability to build relationships within teams, showcasing how you can contribute to the company's success.
Highlight Relevant Skills: In your application, make sure to highlight your proficiency in computer systems and your experience with clinical trial documentation. Mention any specific tools or methodologies you have used in previous roles.
How to prepare for a job interview at Gibbs Hybrid
✨Showcase Your Project Management Skills
Be prepared to discuss your previous project management experiences in detail. Highlight specific projects where you successfully managed timelines, resources, and stakeholder expectations, especially in the context of clinical trials.
✨Demonstrate Your Quality Operations Knowledge
Familiarize yourself with the key aspects of pharmaceutical quality operations. Be ready to explain how your experience aligns with the requirements of managing external Qualified Person (QP) releases and your understanding of the clinical supply chain.
✨Highlight Continuous Improvement Initiatives
Prepare examples of initiatives you've led that focused on process improvement. Discuss the outcomes of these initiatives and how they contributed to operational efficiency or compliance within a clinical setting.
✨Build Rapport with Interviewers
Since relationship-building is crucial for this role, practice your interpersonal skills. Engage with your interviewers by asking insightful questions about their team dynamics and how they collaborate with Regulatory Affairs and Global Clinical Supply Chain.
