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- Tasks: Lead compliance efforts and ensure quality standards at Accord Healthcare's Fawdon facility.
- Company: Accord Healthcare is a rapidly growing pharmaceutical company delivering affordable medicines globally.
- Benefits: Enjoy a competitive salary, bonuses, and a supportive work environment with growth opportunities.
- Why this job: Make a real impact in a dynamic role within a progressive company focused on patient care.
- Qualifications: Qualified Person experience in manufacturing, strong communication skills, and a background in Biologics.
- Other info: Join a diverse team dedicated to innovation and improving healthcare access worldwide.
The predicted salary is between 60000 - 80000 ÂŁ per year.
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Employee Resourcing Partner EMENA at Accord Healthcare
Head of Compliance (Qualified Person)
Role: Full time, Permanent
Location: Fawdon, Newcastle upon Tyne
Salary: Competitive + bonus + benefits
The Role:
Supporting the Director of Quality in maintaining and continuously improving GMDP standards at the Fawdon facility you will ensure current and future EU/UK GMDP requirements are met and that an effective Pharmaceutical Quality system is maintained.
You will build in house know how, capacity and capability within the quality team to support business growth whilst supporting a common Quality Culture and Accord everyday business behaviours to support collaborative working relationships between operations and quality functions.
Leading site inspections and communications with Regulatory Authorities related to GMDP you will support the Quality Management Review process and reporting the site quality performance to senior management and oversee continuous improvement activities to develop and enhance compliance – work with key stakeholders to build a continuous improvement environment and support an ongoing program of change.
To perform the Qualified Person duties in accordance with Directive\” 2001/83/EC (amended by Directive 2004/27/EC) and following the guidance laid down in Annex 16 of Eudralex Volume 4 – Good Manufacturing Practice. ( desirable)
To carry out the routine duties of a Responsible Person in accordance with the EU GDP Guidelines 2013/C 343/01 and to ensure that all conditions of the Wholesaler Distribution Authorisation (WDA) are met.
The Person:
- Qualified Person under the permanent provisions (desirable)
- Experience in working as a qualified person within manufacturing facilities, including batch certification
- A detailed understanding and experience of Biologics and Sterile manufacture and packing and related product transfers
- Experience of importing and certifying products from outside EU
- Experience of hosting MHRA GMDP Inspections
- A decisive thinker and able to progress actions to a schedule
- A practical approach to developing and implementing procedures and processes within a regulated environment
- Strong network of pharmaceutical quality professionals
- An excellent communicator, who can interact effectively on a global level and at all levels within the company
The Rewards:
In return, we offer a competitive salary and rewards package (including holiday, bonus and pension scheme). Not to mention the opportunity to genuinely make a difference in a new and dynamic role within a progressive and expanding business, at an exciting time of growing international reach.
How to Apply:
If you possess the experience, passion and ability to make this role a success then we would like to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. The closing date is 10/08/25. For more information, you can contact us on: careers@accord-healthcare.com
A Bit About Us:
Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients\’ access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide.
To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place; come and join us to make it better.
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All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.
Requisition ID: [[id]]
Seniority level
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Seniority level
Mid-Senior level
Employment type
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Employment type
Full-time
Job function
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Job function
Quality Assurance
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Industries
Pharmaceutical Manufacturing
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Head of Compliance (QP) employer: Accord Healthcare
Contact Detail:
Accord Healthcare Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Compliance (QP)
✨Tip Number 1
Network with professionals in the pharmaceutical quality sector. Attend industry events or webinars where you can meet people who work at Accord Healthcare or similar companies. Building these connections can give you insights into the company culture and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest EU/UK GMDP regulations and guidelines. Being well-versed in these standards will not only boost your confidence during interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 3
Prepare to discuss your experience with hosting inspections and working with regulatory authorities. Be ready to share specific examples of how you've successfully navigated compliance challenges in previous roles, as this will highlight your expertise and problem-solving skills.
✨Tip Number 4
Research Accord Healthcare's recent projects and initiatives. Understanding their current focus areas and challenges will allow you to tailor your discussions during interviews, showing that you're genuinely interested in contributing to their goals.
We think you need these skills to ace Head of Compliance (QP)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Head of Compliance (QP) position. Familiarise yourself with GMDP standards and the specific duties outlined in the job description.
Tailor Your CV: Customise your CV to highlight relevant experience, particularly in compliance, quality assurance, and any specific qualifications related to the pharmaceutical industry. Emphasise your experience as a Qualified Person and any relevant certifications.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the company. Address how your skills and experiences align with Accord Healthcare's mission and values, and mention specific examples of your past achievements in compliance and quality management.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail, which is crucial for this role.
How to prepare for a job interview at Accord Healthcare
✨Understand GMDP Standards
Make sure you have a solid grasp of Good Manufacturing and Distribution Practice (GMDP) standards. Be prepared to discuss how your experience aligns with these regulations and how you can contribute to maintaining and improving them at Accord Healthcare.
✨Showcase Your Experience
Highlight your previous roles as a Qualified Person, especially in manufacturing facilities. Discuss specific examples of batch certification and any experience you have with biologics and sterile manufacturing, as this will be crucial for the role.
✨Communicate Effectively
As an excellent communicator, you’ll need to demonstrate your ability to interact with various stakeholders. Prepare to share examples of how you've successfully communicated complex compliance issues to different levels within an organisation.
✨Prepare for Regulatory Discussions
Since the role involves leading site inspections and liaising with regulatory authorities, be ready to discuss your experience with MHRA GMDP inspections. Think about how you can ensure compliance and foster a culture of continuous improvement in this area.
