Senior QC Analyst Validation Professional

4 weeks ago


Haverhill, Suffolk, United Kingdom EUROAPI Full time

Key Responsibilities

The ideal candidate will be responsible for providing high-quality active ingredients that meet the highest pharmaceutical regulatory and compliance standards.

This position involves working closely with the QC management team to assign and manage project resourcing, as well as collaborating with R&D, clients, and key stakeholders to manage key analytical projects.

The candidate will be responsible for owning analytical projects and deputizing for leadership, working with R&D, clients, and key stakeholders. They will also develop, train, and report validation and transfer activities within QC for new and existing clients.

Our Requirements

The successful candidate will have a strong background in pharmaceutical sciences and a high level of experience handling HPLC, GC, FTIR, UV, PXRD, and DSC. They will also have GMP knowledge and experience of analytical method validation & transfer principles.

What we Offer

We offer a competitive hourly rate and retention bonus, as well as training and development opportunities. The candidate will work 36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm, and will have the opportunity to work on a 23-month contract term.

About EUROAPI

EUROAPI is a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio. We are focused on reinventing active ingredient solutions to sustainably meet customers' and patients' needs around the world.

We have six manufacturing sites located in Europe, and our Haverhill (UK) site has been established for forty years. We employ over 250 people and have built a strong reputation in Flow Chemistry, Active Pharmaceutical Ingredient (API) Spray Drying, and as a Contract Development and Manufacturing Organisation (CDMO).



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