Stability Technician

BELIEVE IN LIFE. Join a company that takes you further!

Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality, affordable pharmaceuticals worldwide.

People are the key to our present and future success, so we carefully select candidates who meet the requirements for each position and who also align with our cultural DNA and values.

Here’s an overview of what your role will entail (spoiler alert: it’s awesome!)

We are looking for a Stability Technician to join our Laboratory Team.

What you'll be responsible for:

1. Revision of stability reports issued for R&D projects conducted by R&D (lab) and/or performed by external companies.
2. Organizing, managing, and reviewing stability reports and results as part of Technical Transfers generated at 2nd CMOs, including follow-up for Galenicum’s factory (SAG Manufacturer).
3. Management and review of ongoing stability studies (products controlled or released by the lab, products manufactured in third CMOs, or products where Galenicum is involved only as a broker).
4. Evaluation of trends and pourabilities regularly to detect tendencies and take preventive actions with CMOs.
5. Revision and approval of stability protocols and reports, and follow-up of stability results at each time point.
6. Updating results in a common platform accessible by all departments.
7. Informing relevant departments of any expected deviations and coordinating new analyses if necessary.
8. Creating and maintaining SOPs related to these activities and training staff accordingly.

What you bring to the team:

1. Minimum 2-3 years of experience in analytical development within a GLP/GMP environment, with proven experience in developing and validating analytical methods such as HPLC, UPLC, LC-MS, GC, UV, DSC, PSD, potentiometric titration, UV-Vis, IR, AA, KF titrations, and dissolution tests.
2. Experience in monitoring stability studies, analytical transfers from CROs to CMOs, and compiling technical documentation for international MA approvals.
3. Valuable knowledge of international guidelines such as EMEA, FDA, ICH, and ISO.
4. Proficiency in MS Office.

Educational qualifications:

1. Bachelor’s degree in life sciences, preferably Chemistry.
2. Master’s degree in Analytical Chemistry and/or Pharmaceutical Industry.
3. Fluent in English and Spanish, spoken and written.

Your key strengths:

1. Motivated, proactive, dynamic, methodical, organized, and decisive.
2. Self-sufficient with influencing and leadership skills.
3. Strong analytical and problem-solving skills.
4. Highly responsible, capable of working under pressure to meet deadlines.
5. Excellent multitasking, organizational, planning, and time management skills.
6. Detail-oriented with strong communication and research skills.

We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you?

Come aboard. Believe in life!