Apothecon Group is a vertically integrated CDMO delivering end-to-end capabilities from Molecule to Market, anchored by a strong track record of global regulatory compliance. With a combined presence in India and the United States, the Group comprises three key entities: Apothecon Pharmaceuticals Pvt. Ltd. (Vadodara, Gujarat, India), Navinta LLC (Ewing, New Jersey, USA), and Navinta III Inc. (Boca Raton, Florida, USA).
Supported by robust R&D capabilities and deep expertise in complex molecules, Apothecon Pharmaceuticals serves as the Group’s global CDMO hub for Active Pharmaceutical Ingredients (APIs), Finished Dosage Forms (FDFs), and peptides. This expertise is further extended through Navinta (https://www.navinta.com/), whose state-of-the-art sterile injectables capabilities and scientific depth enable the development and commercialization of complex products.
Together, the Group offers a regulatory reach in 100+ countries, offering a diversified portfolio of 35+ API products, 20+ FDFs, and 25+ products in the R&D pipeline across 8+ therapeutic areas.
DATE AND TIME:
DATE:Saturday, 24 October 2026
TIME:10:00 am to 4:00 pm
VENUE:Padra-Jambusar Highway, Village Dabhasa, Tal. Padra, Dist. Vadodara, Gujarat 391440
Interested candidates, share your CV on
hrd@apotheconpharma.com
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JOB DETAILS:
Open positions
Wet Lab Analyst
2-4 years
Auto-Titrator, Karl Fischer, FTIR and UV exposure
HPLC/GC Analyst
5-7 years
HPLC and GC analysis, Empower software exposure is an advantage
Reviewer, Documentation & Data Review
5-7 years
Extensive QC documentation review, data review in Empower
4-7 years
HPLC Analyst, Stability & AMV
HPLC with Empower, stability analysis, method validation (formulations)
Qualification: B.Sc, M.Sc, B.Pharm or M.Pharm
Background: only from regulatory compliance-oriented pharma organizations (US FDA, MHRA or WHO-GMP audited)
Bring a printed CV, photo ID and your certificates on the day.
Those who have already appeared in the last six months need not apply.
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