— Join Binova Pharma
The work is consequential. The standards are non-negotiable.
We staff every function — formulation, GMP operations, regulatory compliance — with professionals who understand that a batch record is not paperwork. It is the chain of custody between our process and a patient's daily regimen.
Process discipline is the culture
Every release record is reviewed
Compliance is the baseline, not a ceiling
Stable environments produce reliable outcomes
Regulatory standards define the floor. Our internal protocols go further — because the patients relying on our formulations need consistency that outlasts any single inspection cycle.
Our QA team signs off on every lot before it leaves the facility. We measure success by release rates and deviation frequency, not speed-to-market.
We do not optimize for disruption. Long-term roles, documented career tracks, and teams that stay because the work itself is meaningful.
Roles built on documented discipline
Formulation Chemistry
GMP Operations
Regulatory Compliance
Develop and validate API dosage forms for chronic-disease indications. Requires solid-state chemistry expertise and familiarity with ICH stability protocols.
Operate and maintain production lines under current Good Manufacturing Practices. Batch documentation accuracy and deviation reporting are core expectations.
Manage NDA/ANDA submissions, FDA correspondence, and post-approval change controls. Experience with 21 CFR Parts 210 and 211 required.
If the batch record matters to you, you belong here
Send your CV and a brief note on your GMP experience to careers@binovapharma.com — or use the link below to see every currently posted role.