Job Title:  NPL Quality Lead

Role Details

New Product Launch Quality Lead – Pharmaceutical

Role: Full-time, permanent

Location: Can be based at any of the Accord sites – Barnstaple, Fawdon or Uxbridge

Salary: Competitive Salary + bonus + significant benefits

The Role

Due to the continued increase in our portfolio of products, we have an exciting new role available, we’re looking for a dedicated and organised New Product Launch Quality Lead to project manage and oversee all launches, acting as the coordinator and provider of Quality and GMDP expertise for the EMENA region.

In this role, you’ll ensure all new products are compliant with UK/EU/EMENA applicable regulations and make sure that there is clear ownership and accountability being taken for the timely and compliant execution of all associated Quality activities across the respective corporate site/affiliate for the Quality functions supporting all launch activities.

Taking responsibility for and managing the QA elements of New Product Launches, coordinating all activities, liaising with internal stakeholders as well as suppliers and service providers, and maintaining complete visibility of supply chains for new products ensuring new supplier and new product set up. You’ll build and maintain good working relationships with all parties ensuring all are aligned and that we succeed in a smooth and timely launch to market.

The Person

• Significant experience in Pharmaceutical Quality based roles in UK and EU GMDP
• Strong knowledge of UK/EU Quality regulatory compliance requirements
• A practical approach to developing and implementing procedures and processes within a regulated environment
• Experience of acting as an SME during competent authority GMDP Inspections
• An excellent communicator, with demonstrated stakeholder management skills, who can interact effectively at all levels within the company
• A decisive thinker and able to progress actions to a schedule

• Good communication skills in both spoken and written English.
• Must be able to select appropriate quality and auditing tools and techniques and use them in a variety of scenarios.
• Must be able to verify, document and communicate audit results, develop an audit report and evaluate the effectiveness of corrective action and follow up.
• Extensive experience of working within a Quality Related Role in the Pharmaceutical Industry.
• Flexible with working hours and able to travel on a regular basis throughout Europe and internationally as and when required.

How to Apply

If you have the experience, passion and ability to make this role a success then we would love to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. The closing date is 13th April 2025. For more information, you can contact us on: careers@accord-healthcare.com

A Bit About Us

Accord Healthcare 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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