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- Tasks: Ensure compliance with regulations and maintain inspection readiness in a collaborative environment.
- Company: Join a global biopharmaceutical leader focused on innovative healthcare solutions.
- Benefits: Enjoy remote work options, competitive referral schemes, and a chance for career growth.
- Why this job: Be part of a dynamic team making a real impact in healthcare innovation.
- Qualifications: 4+ years in GCP Quality roles with experience in audits, inspections, and SOP writing.
- Other info: Open to all qualified candidates; diversity is valued here.
The predicted salary is between 48000 - 72000 £ per year.
Role Title: 2x Process Quality Specialist Location: Remote in the UK or Hybrid in Uxbridge
Contract Length: 12 Months with an high chance of extension/going permanent
Our client is a global biopharmaceutical company, specializing in the discovery and development of innovative medicines and solutions for severe diseases such as neurology and immunology. Joining this company means becoming part of a dynamic and forward-thinking organization committed to making a difference in healthcare. With its strong emphasis on innovation, collaboration, and patient impact, Our client offers a fulfilling career for those passionate about creating solutions that improve lives globally.
In this role you will work in collaboration with Clinical Development Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with ICH GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness. Minimum 4 years of experience in a GCP Quality Role
Experience with GCP audits & Inspections experience
Gap analysis experience & Experience writing SOPs
Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Clinical Quality Manager/ Senior Quality Manager employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Quality Manager/ Senior Quality Manager
✨Tip Number 1
Make sure to highlight your experience with GCP audits and inspections during any discussions. This is a key requirement for the role, and demonstrating your familiarity with these processes can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those who have worked in quality roles. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during interviews.
✨Tip Number 3
Stay updated on the latest ICH GCP, GLP, and PV regulations. Being knowledgeable about current compliance standards will not only help you in the role but also impress the hiring team during your conversations.
✨Tip Number 4
Prepare to discuss specific examples of gap analysis you've conducted and SOPs you've written. Concrete examples will demonstrate your hands-on experience and problem-solving skills, which are crucial for this position.
We think you need these skills to ace Clinical Quality Manager/ Senior Quality Manager
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Clinical Quality Manager position. Understand the key responsibilities and required qualifications, especially the emphasis on GCP compliance and experience with audits.
Tailor Your CV: Customize your CV to highlight relevant experience in GCP Quality roles, audits, and SOP writing. Use specific examples that demonstrate your expertise and how it aligns with the company's focus on innovative medicines.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for improving healthcare. Mention your understanding of the company's mission and how you can contribute to their goals.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors or typos, as attention to detail is crucial in quality management roles.
How to prepare for a job interview at Planet Pharma
✨Understand GCP and Regulatory Standards
Make sure you have a solid grasp of Good Clinical Practice (GCP) and relevant regulatory standards. Be prepared to discuss how your experience aligns with these regulations and how you've ensured compliance in previous roles.
✨Showcase Your Audit Experience
Highlight your experience with GCP audits and inspections. Prepare specific examples of audits you've conducted or participated in, and be ready to discuss the outcomes and any improvements you implemented.
✨Demonstrate Your Problem-Solving Skills
Be ready to talk about your experience with gap analysis and how you've identified and addressed compliance issues in the past. Use concrete examples to illustrate your analytical skills and proactive approach.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask about the company's approach to quality management and their expectations for the role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
