Main Responsibilities

Follow-up and supervision of ICH and ongoing stability studies, in‑use stability studies and photostabilities, among others.
The management of the assigned projects, keeping the deadlines and establishing 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

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 Fisher titration, and UV‑Visible spectrophotometry.
Familiarity with GMP and GLP guidelines.
Ability to work as part of a team.
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).

Benefits

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).
Headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, with a rooftop terrace.

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that 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.
#J-18808-Ljbffr