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Stability 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 Group

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés- Barcelona), Italy (Monsano-Ancona), and Germany (Frankfurt) and a Liasson office in South Korea (Seoul), offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA.

KYMOS GROUP is devoted in providing high quality and added value services to its partners and it is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies.

KYMOS GROUP has a young and dynamic staff of more than 250 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

Job description

We are hiring a Stability Scientist for our Chemical Analysis and Quality Control Department.

Main responsibilities include:

  • Follow-up and supervision of ICH and On going stability studies, in-use stability studies and photostabilities, among others.
  • The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
  • Technical document writing associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.)
  • The direction and supervision of the experimental work of the technical staff in charge.

 

 

 

Requirements

Requirements: 

  • Degree in Analytical Chemistry
  • Minimum of 2 years’ experience in a similar role within Analytical Development and/or Quality Control in the pharmaceutical industry.
  • Practical experience with HPLC/UHPLC, GC, and core analytical techniques such as dissolution testing, potentiometry, Karl Fischer titration, and UV-Visible spectrophotometry.
  • Familiarity with GMP and GLP guidelines.
  • Ability to work as part of a team.
  • A proactive person with strong problem-solving skills.
  • English level equivalent to the Cambridge First Certificate (B2).
  • Availability to work the afternoon shift (2:00 PM – 10:00 PM).

 

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.

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