API and intermediate manufacturing runs on multi-step, cGMP-compliant synthesis with strict batch record documentation, analytical method validation and audit readiness for USFDA, EU-GMP and WHO-GMP inspections. Potent or hazardous intermediates require containment engineering and occupational exposure band (OEB) classification, and most plants are moving toward solvent recovery and greener process routes.
Hiring in this space is compliance-first: a chemist may be technically excellent but still be a poor fit if they cannot operate inside a regulated documentation culture.
Regulated, documented synthesis routes for APIs and advanced intermediates.
Audit-ready documentation, batch records and DMF/ANDA filing support.
OEB-classified containment and EHS controls for hazardous intermediates.
We evaluate candidates on documentation discipline and audit exposure, not chemistry skill alone.
Our regulatory affairs shortlists come pre-screened for DMF/ANDA filing experience.
We source EHS professionals specifically experienced with potent/OEB-classified compound handling.
Access to professionals who have been through live USFDA/WHO-GMP inspections, not just training decks.
Talk to a recruiter who already understands the process, the compliance load and the talent pool.
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