VALIDATION OFFICER - PHARMACEUTICALS

Role: Full time, 12-month fixed term contract
Location: Barnstaple, Devon
Working Hours: Monday – Friday (08:00-16:30)
Salary: Circa. £39,500pa subject to experience + bonus + significant benefits

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 click on the ‘apply’ button to submit your application. The closing date is 17th April 2025. 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.
Job Types: Full-time, Fixed term contract
Contract length: 12 months
Pay: From £39,500.00 per year

Additional pay:

• Bonus scheme

Benefits:

• Company pension
• Employee discount
• On-site parking

Schedule:

• Day shift

Ability to commute/relocate:

• BARNSTAPLE: reliably commute or plan to relocate before starting work (required)

Work Location: In person
Application deadline: 17/04/202

We’re seeking a meticulous and pragmatic Validation Officer to support our on-going company growth and contribute to the continuous improvement of our systems and procedures. In this varied role, you’ll apply scientific principles to a diverse range of projects and processes, making a significant contribution to the quality compliance of the business. You’ll work as part of a team on validation activities across the lifecycle of our products and be supported by tailored training and mentoring to facilitate your development. On a daily basis, this means you could be helping us bring new products or equipment to the site, proving safety and consistency in manufacturing (writing protocols, testing product, generating and handling output data and resolving any deviations). By supporting on cross-functional projects, you’ll work closely with a broad range of departments across the business to ensure work is completed to the required regulatory and GMP (Good Manufacturing Practices) standards, whilst maintaining all validation documents, systems and procedures. In addition, you’ll interpret our Production and QC data, distilling it to an easily understandable format and presenting it to management, regulatory authorities or customers. This role is a great opportunity to broaden your knowledge and gain experience in a diverse role within the pharma industry.