At a Glance
- Tasks: Support quality and compliance in a global pharmaceutical company, ensuring inspection readiness.
- Company: Join a leading biopharmaceutical company focused on severe diseases in immunology and neurology.
- Benefits: Enjoy a hybrid work model with competitive pay and opportunities for professional growth.
- Why this job: Be part of impactful projects that enhance patient safety and compliance in the pharmaceutical industry.
- Qualifications: Strong pharmaceutical experience and knowledge of GCP, with FDA/EMA inspection readiness essential.
- Other info: This role requires entitlement to work in the UK and may involve a DBS check.
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: 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 Your Background : • 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 on 01438 870011 or email pharmacontracts@ckagroup.co.uk. 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.
Process Quality Excellence Specialist 14257 (3) employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Quality Excellence Specialist 14257 (3)
✨Tip Number 1
Familiarize yourself with the latest regulations and guidelines related to GCP, GLP, and PV. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality excellence.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in Quality Assurance or Clinical Development. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios related to audit and inspection readiness. Being able to discuss your hands-on experience in these areas will set you apart from other candidates.
✨Tip Number 4
Showcase your ability to collaborate with various stakeholders by preparing examples of past experiences where you successfully worked with cross-functional teams. This is crucial for the role as it involves working closely with Global Quality and other departments.
We think you need these skills to ace Process Quality Excellence Specialist 14257 (3)
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Process Quality Excellence Specialist position. Understand the key responsibilities and required qualifications, especially the importance of GCP and compliance experience.
Tailor Your CV: Customize your CV to highlight relevant pharmaceutical experience, particularly in Quality Assurance or Clinical Development. Emphasize any hands-on experience with GCP audits and inspections, as well as FDA/EMA inspection readiness.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the specific requirements of the role. Mention your experience with quality and compliance policies, SOPs, and your ability to collaborate with various stakeholders.
Highlight Compliance Knowledge: In your application, make sure to showcase your understanding of international regulations such as ICH GCP, GLP, and PV. This will demonstrate your readiness to ensure compliance and inspection preparedness.
How to prepare for a job interview at CK Group
✨Understand the Regulatory Landscape
Familiarize yourself with the International Council for Harmonization (ICH) guidelines, especially GCP, GLP, and PV. Being able to discuss these regulations confidently will demonstrate your expertise and readiness for the role.
✨Showcase Your Audit Experience
Prepare to share specific examples of your experience with global GCP audits and inspections. Highlight any challenges you faced and how you overcame them, as this will illustrate your problem-solving skills and attention to detail.
✨Emphasize Collaboration Skills
This role requires working closely with various stakeholders. Be ready to discuss past experiences where you successfully collaborated with teams, particularly in quality assurance or clinical development settings.
✨Prepare for Scenario-Based Questions
Anticipate questions that may ask how you would handle specific situations related to quality compliance or audit preparation. Practicing your responses will help you articulate your thought process and decision-making skills effectively.