Quality Control Scientist (Morning Shift)

Kymos Group; Barcelona; Híbrido; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Scientist in Chemical Analysis to join their Quality Control department. This exciting role involves conducting and supervising studies on analytical methods for drug control and stability studies, using techniques such as HPLC and GC. The ideal candidate will have a strong educational background in Chemical Sciences and experience in quality control within the pharmaceutical sector. Enjoy a dynamic work environment with flexible hours, professional development opportunities, and a culture that embraces diversity and inclusion. Join a team where your contributions will make a significant impact on pharmaceutical quality and safety.

Servicios

Flexible Working Hours

Professional Development

23 Vacation Days

Fully Stocked Canteen

Rooftop Space

Employee Benefits Flexibility Platform

Formación

• Bachelor's degree in Chemical Sciences with analytical orientation required.
• Experience in quality control and analytical method validation is valued.

Responsabilidades

• Conduct studies on the development and validation of analytical methods.
• Ensure compliance with GLP and GMP regulations in all analyses.

Conocimientos

HPLC

GC

Analytical Method Development

Quality Control

GLP and GMP Compliance

English Proficiency

Educación

Bachelor's in Chemical Sciences

Master's in Chemical Sciences

Herramientas

Potentiometry

Karl Fischer

UV Spectroscopy

Dissolution Testing

Descripción del empleo

Kymos is hiring a Scientist in Chemical Analysis for our Quality Control department :

Position Description :

• We offer a position in the Pharmaceutical Chemical Analysis Department as a Scientist responsible for the analysis of active ingredients and pharmaceutical specialties.
• The role involves designing, supervising, and conducting studies on the development and validation of analytical methods for drug control, stability studies, quality control, etc. Analytical techniques employed include HPLC, GC, potentiometry, Karl Fisher, UV, dissolution testing, etc.
• The work is conducted in compliance with GLP and GMP regulations.

Profile of the required person :

• We are seeking an individual with a Bachelor's degree in Chemical Sciences (Analytical Orientation). A Master degree is highly valued.
• The ideal candidate has some knowledge in HPLC, GC techniques, and have a basic understanding of an analytical development department.
• Some experience in the development and validation of new analytical methods for quality control of pharmaceuticals is valued.
• Previous experience in chemical analysis of active ingredients and pharmaceutical formulations in a Quality Control or Analytical Development department of a pharmaceutical or related company is preferred.
• Experience working with GLP and GMP is required.
• Minimum English language proficiency level : First Certificate.
• Availability for morning shift (6pm-14pm).

If you join us, you will enjoy :

• Working in a dynamic company with a highly qualified growing team
• Professional development and collaborative environment and a culture of empowerment.
• Flexible Working Hours and intensive schedule on Friday.
• Hybrid work, but mainly in the office.
• Access to the employee benefits flexibility platform.
• 23 vacation days per year plus 24th and 31th of December.
• Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
• Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic