Analyst (Remote working)

Olon; A distancia; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A pharmaceutical company is seeking a qualified candidate for a Scientific role at its Murcia site in Spain. The successful individual will perform HPLC and GC analyses and provide analytical support to R&D. Essential qualifications include a degree in Chemistry or a PhD and fluent English. The ideal candidate should possess at least 2 years of relevant experience, excellent laboratory, and communication skills. This role demands strict adherence to quality and regulatory standards in a fast-paced environment.

Formación

• Minimum of 2 years of experience in HPLC and GC analysis.
• Experience in a GMP environment is a plus.
• Excellent laboratory skills are required.

Responsabilidades

• Perform HPLC and GC analyses for raw materials and products.
• Provide analytical support to R&D on method selection.
• Prepare analytical reports and documentation for projects.

Conocimientos

HPLC analysis

GC analysis

Analytical method development

Communication skills

Fluent English

Educación

Degree in Chemistry or PhD in Analytical Chemistry

Descripción del empleo

dedicated to the manufacturing and marketing of APIs and advanced intermediates.

For our Murcia site in Spain, we are looking for

to fill a vacancy in the Scientific Area.

Reporting to the Scientific Director, the successful candidate will be responsible for :

Performing

HPLC and GC analyses

a minimum of 2 years of experience in these techniques is highly valued).

Providing analytical support to R&D, selecting the most suitable analytical methods for the analysis of raw materials, IPCs, intermediates, and final products, as well as assisting in impurity analysis.

Collaborating with R&D researchers in day-to-day investigations.

Preparing R&D analytical reports and MoAs for projects developed within R&D.

Additional skills considered a plus :

Developing analytical methods for new processes carried out in the R&D Department and coordinating validation activities.

Validating analytical methods for raw materials, IPCs, intermediates, and final products.

Preparing documentation related to method development and validation (protocols, validation reports, etc.).

Ensuring strict compliance with regulations related to safety, environmental protection, and quality.

Requirements :

Degree in Chemistry or PhD in Analytical Chemistry.

Excellent laboratory and communication skills.

Fluent English, both written and spoken, is essential.

Relevant industrial experience in analytical method development and work experience in a GMP environment are considered a plus.

What we offer :