Analytical Development Scientist
Join Euroapi as an Analytical Development Scientist supporting Analytical Technology Transfer for the Haverhill site. You will be joining an R&D centre of excellence at a newly formed CDMO. We work passionately to develop, manufacture, and supply active ingredient solutions for our healthcare partners around the world. You will ensure we are one step ahead in the race for innovation and leading the way in developing active pharmaceutical ingredients sustainably across Europe and beyond meeting the highest quality standards.
Your Responsibilities
You will:
- Develop and validate new analytical methods.
- Reassess and improve current methods.
- Be a go-to expert for chemical analysis, especially for the methods you develop.
- Solve complex analytical problems within R&D and QC environments.
- Train R&D and QC team members in new methodologies.
Our Company
EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities.
Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries.
EUROAPI is listed on Euronext Paris.
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
Masters Degree in Chemistry, Analytical Chemistry, Pharmaceutical Science or a related subject, or relevant industrial experience.
Experience in running methods using a range of techniques: HPLC, GC, LC-MS, GC-MS or other techniques such as titration, FT-IR.
Method development experience.
Strong record-keeping skills.
Ability to write reports and derive appropriate conclusions from results.
Demonstrable experience of achieving goals together with a client or stakeholder focus and excellent relationship building skills.
Method validation experience would be advantageous but not essential.
What we offer
- Competitive hourly rate
- 12-month contract starting in July or August
- 36 hours per week, 9-5.30pm Monday-Thursday, 9-4pm Friday
- Training and development
Apply Today!
Find out more about this exciting opportunity, apply today or contact Marie Meekings.