Quality Control Scientist (Afternoon Shift)

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality
Work modality: On site

Kymos

We are an innovative and fast-growing CRO offering you the opportunity to develop your career in an excellent working environment. Kymos Group is a scientific-technical services company directed to companies of the chemical-pharmaceutical and veterinary sector.

KYMOS offers a wide range of analytical services in Medicinal Chemistry to optimize the research, the development and the quality control for innovative, generic and biological drug substances and drug products from the preclinical stage to market.

KYMOS also has an extensive experience in developing and validating bioanalytical methods and sample analysis in any biological matrix using the latest technology. Mass spectrometry and immunology laboratories are available to carry out small molecule and biologic projects.

KYMOS is also an international group, Kymos Group, with sites in Italy, PHARMAPROGRESS and in Germany, PROLYTIC.

Job description

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.

Requirements

Profile of the required person:

We are seeking an individual with a Bachelor's degree in Chemical Sciences (Analytical Orientation). A Ph.D. 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 afternoon shift (2pm-10pm).

Job closed

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality
Work modality: On site

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