Job description
Join the Small Molecule Method Development (SMMD) group within the Analytical Development department, part of the Therapeutics Development & Supply organization. The SMMD team is composed of scientists passionate about developing, validating, and transferring analytical methods for Small Molecule drug characterization throughout their lifecycle — from early development to commercialization.
The group acts as a center of excellence for chromatographic and physicochemical testing and leads the implementation of innovative analytical technology platforms for New Molecular Entities. You will work in a laboratory-based environment alongside experts in Gas Chromatography (GC), GMP, and analytical development, ensuring the reliability and robustness of analytical methods used to guarantee patient safety.
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Your missions
* Coordinate and execute analytical gas chromatographic work, including method development, validation, and transfer.
* Contribute to expanding the team’s analytical expertise towards new modalities.
* Assess and implement newly marketed GC methodologies and equipment.
* Manage assigned projects independently in line with project and team deliverables.
* Apply state-of-the-art scientific knowledge during investigations and troubleshooting.
* Ensure compliance with GMP, safety, and regulatory requirements.
* Guarantee accurate GMP documentation, including data review, protocols, and report writing.
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Your profile
* Education: Bachelor’s or Master’s degree or PHD in chemistry, analytical chemistry, biomedical laboratory technology, or a related field.
* Experience: 1 to 3 years of experience in Gas Chromatography and analytical development or a related laboratory environment.
* Skills:
o Ability to work both independently and collaboratively.
o Excellent communication skills, verbal and written.
o Results- and performance-oriented mindset.
o Technical knowledge of gas chromatographic systems and physicochemical techniques.
o Understanding of method development, validation, and transfer for APIs and GMP investigational testing.
o Awareness of cGMP regulations and practical experience in their implementation.
o Proficiency in English (oral and written).
o Ability to adapt to a dynamic, fast-paced environment.
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What we offer
* Work in a multicultural environment fostering personal and professional growth.
* Access to continuous training and development programs through the Amaris Academy.
* A dynamic career path with international mobility and real growth opportunities.
* A company culture centered around meritocracy, intrapreneurship, and inclusion.
* A strong focus on people, with regular follow-ups, mentorship, and tailored development plans.
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At Amaris Consulting, we believe in diversity, equity, and inclusion. We are committed to creating an environment where everyone feels valued, respected, and empowered to contribute their unique perspectives to our collective success.