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Location
In office (Budapest)
Seniority
Staff · 10+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Apr 14, 2026. EUROAPI scores A on the Alion truth index.

Overview
Company
Impact
Profile match
EUROAPI is the leading small molecules player with about 200 active pharmaceutical ingredients, offering one of the largest portfolios in the industry, while developing innovative molecules through CDMO activities.

Analytical DevelopmentScientific Lead

We are looking for an experienced professional who enjoys coordinating analytical development activities, supporting product development, and collaborating actively with international partners.

Key Responsibilities:

  • Provide analytical support for EUROAPI R&D development projects, including chromatographic, titration, spectroscopic, and other analyticaltechniques;

  • Apply EUROAPI R&D international guidelines and management expectations in dailywork;

  • Participate in the development and/or adaptation of new analytical methods for testing products under development, in line with regulatory requirements and customer needs; coordinate method validationactivities;

  • Organize analytical testing of products, intermediates, and materials used in manufacturing at various stages of development; collect, systematize, and analyze trends in results; communicate findings to developmentunits;

  • Perform quality assessments of products under development and issue the required certificates ofanalysis;

  • Summarize analytical experience and oversee the preparation, review, and approval of procedures and qualityspecifications;

  • Conduct professional discussions with international partners on product quality and quality controlmatters;

  • Coordinate analytical development activities related to industrialtechnologies;

  • Review methods used forinprocesscontrol;

  • Review quality and quality control sections of technologicaldocumentation;

  • Activelyparticipatein site and R&D investigations and handle OOScases;

  • Initiate and coordinate stability studies related to R&D developmentprojects;

  • Organize preparation for audits andparticipateactively inaudits;

  • Maintain close contact and cooperation with organizational units involved in development activities, as well as other analytical groups withinEUROAPI;

  • Participate inidentifyingdevelopment needs of team members, preparing training plans, and onboarding newcolleagues;

  • Propose instrument procurement andmodernization;

  • Participate in planning projects related to the professional area and in preparing cost estimates.

Requirements:

  • Higher education degree in a relevant field; a PhD and/or a relevant second degree is anadvantage;

  • Minimum 10 years of professional experience; international pharmaceutical development experience ispreferred;

  • Confident,businesslevelEnglishproficiency;

  • Proficient computerskills;

  • Ability to work independentlyand in a structured manner, as well aswillingness to lead a professional team.

Why Join Us?

  • According to the company's Cafeteria policy, gross 636000 HUF/year (also during the probationary period)

  • Company bonus (average 8% of the annual salary)

  • Annual medical check at the Buda Health Center, for which we provide 1 paid day off

  • Sports facilities (sauna, fitness room)

  • Collective life and accident insurance

  • Voluntary pension fund membership (supplemented with employer contribution)

  • Free parking

  • Office massage

Place of work: Budapest, Hungary

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