Qualified Person

Are you a Qualified Person looking for a role releasing packed batches for secondary operations and certifications for spray dried intermediates for a CDMO business? You will conduct lab investigations and provide certifications for semi-finished products, blisters, vials & steriles. Apply today!

Your Responsibilities

You will:

• Ensure compliance within the Haverhill operation in line with the requirements of the manufacturing licence.

• Proactively develop your knowledge on a continued basis in areas such as dosage forms, manufacturing processes and the relevant cGMPs and seek to develop and coach others.

• Develop a deep technical and professional knowledge of all the relevant company processes and quality management systems in respect to upstream manufacturing activities to ensure you can certify and release finished investigational drug products.

• Collaborate with Manufacturing and Regulatory Affairs to provide support for license submissions and review the CMC requirements to ensure correct distribution practices.

• Provide guidance and work with Senior Leaders to resolve complaints, deviations or product recalls ensuring best practice across the site.

Our Company

EUROAPI is a new player in Active Pharmaceutical Ingredients (API), carve out from Sanofi with the purpose of becoming a worldwide champion in API commercial and Contract Development and Manufacturing Organization (CDMO) activities.

Taking action for health by enabling access to essential therapies inspires our 3,350 people every day. Headquartered in Paris, Euroapi include 6 European API production sites located in Brindisi (Italy), Frankfurt (Germany), Haverhill (UK), St Aubin les Elbeuf (France), Budapest (Hungary) and Vertolaye (France).

The EUROAPI Haverhill (UK) site has been established for forty years, located fifteen miles east of Cambridge and sixty miles north of London, within the golden triangle. It employs over 250 people and has built a strong reputation in Flow Chemistry, Active Pharmaceutical Ingredient (API) Spray Drying and as a Contract Development and Manufacturing Organisation (CDMO). Haverhill is proud to house the world’s largest, continuous production, pharmaceutical spray dryer and performs secondary packaging and release activities for oncology and rare disease medicines supporting global markets. The site also offers a contract testing and release facility within its laboratories.

Our Requirements

You will be eligible to act as a QP in the UK.

You will have experience working in biologics, sterile drug manufacturing, solid dose or vaccines.

Knowledge of spray drying processes would be beneficial.

Full time (36 hours per week)

Your Benefits

• Attractive Salary

• Competitive benefits

• Training & Development

• 36 hours per week, 9-5.30pm Monday to Thursday, 9-4pm Friday

• Onsite subsidised restaurant

Culture & Values

We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right".

Diversity & Inclusion

EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination.

Environment, Social and Governance

We strongly believe that the success of our company lies in its capacity to adapt to tomorrow’s challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain.

Apply Today!

Find out more about this exciting opportunity, apply today or contact Marie Meekings.

Do you know someone for this role?

We are accountable for the success of Euroapi and that means finding the best people that share our values. Refer a candidate today or talk to your HR Business Partner to find out more.