Competitive Salary & Company Benefits | Petersfield

Monday to Friday, 9.00am - 5.00pm (potential for flexibility on start/end times based on 7.5hrs/day)

Are you looking to work for a rapidly growing UK Pharmaceutical company, who are passionate about improving patients’ lives across the world? 

Aspire Pharma is an asset-light pharmaceutical manufacturer. It licenses and develops niche pharmaceutical products that offer innovative formulations, value for money for payors, and reliable supply arrangements in markets which are often underserved. The business has a highly diversified portfolio of more than 250 products across a number of categories, including branded specialty products and unbranded niche generics in therapeutic areas such as urology, ophthalmology, CNS and dermatology.

Do you want to be part of the journey?

If so, here is your chance!

The Role

Responsible for supporting R&D with the procurement of R&D samples and reviewing product development reports, analytical data, bioavailability (BA) and bioequivalence (BE) studies. You will collaborate and build close relationships with R&D labs, Contract Manufacturing Organisations (CMOs) and Contract research Organisations (CRO). The R&D Associate will coordinate with many external parties, developing studies, ensuring timelines and costs are controlled and communicated as appropriate. Work is based in Petersfield, with some travel within the UK, EU, and India.

What will you be doing?

• Project Management – Expectation to drive and manage projects. Coordinating timelines, costs, and archive documents to ensure that studies progress to expected timelines. Ensure budgets and timelines are managed effectively.
• Alliance Management – Create lasting relationships with external partners. Collaborate with CMOs, contractors, and developers.

• Communication – Ability to review documents from regulatory affairs, clinical and marketing. To effectively communicate scientific ideas in written and verbal format. Clear and timely communication of changes in timelines, budget, and communicate risks.
• Regulatory Affairs – Comply with GMP/GDP/GCP and GXP.
• Quality Policy – Comply with the company Quality policy and internal processes. Provide support to the Quality Team in SOPs. Manage and control of R&D sample requests.

The Person

• Excellent collaboration, communication, and people skills.
• Flexible can-do attitude.
• Strong problem-solving skills and logical approach.
• Excellent organisational skills.

Why join us?

As well as a fantastic, inclusive company culture, where employees are truly valued and a competitive salary, we also offer an ever-improving benefits scheme to support your physical and mental well-being which include:

• Generous Pension Scheme.
• Life Assurance cover and Employee Assistant Program.
• 25 days’ holiday plus Bank Holidays.
• Learning and Development opportunities.
• Excellent opportunities for progression.
• Fantastic Company events and celebrations throughout the year.