Live opening · Posted 7 hours ago

Manager SAP EWM

Rubicon Research Limited · Thane, Maharashtra, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 7 hours ago
CompanyRubicon Research Limited
LocationThane, Maharashtra, India (On-site)
Work modeNo
SkillsSAP
SourceLinkedin
ListedPosted 7 hours ago

About the role

Description supplied by the original job listing.

Company Description Rubicon Research Limited is an IP-led pharmaceutical company that develops value-added products for global partners and builds its own portfolio of generic prescription and OTC medicines across diverse therapeutic areas. The company leverages proprietary drug delivery technologies and advanced formulation expertise to solve complex product development and delivery challenges. Its portfolio covers multiple dosage forms, including oral solids and liquids, ophthalmic, nasal, injectable, topical, drug–device combinations, and fixed-dose combinations, with 50+ patents and dozens of approved and in-development products for the US market. Rubicon Research operates state-of-the-art, GMP-compliant R&D and manufacturing facilities in India and Canada, and maintains a business development and regulatory office in the United States. The organization also invests in healthcare innovation and professional learning through Rubicon Consumer Healthcare and Rubicon Academy.
Role Description This is a full-time, on-site role based in Mumbai. The Job Title will support pharmaceutical product development and related activities, collaborating with cross-functional teams such as R&D, quality, manufacturing, and regulatory affairs. Day-to-day responsibilities may include planning and executing project tasks, analyzing data and documentation, preparing technical reports or presentations, and contributing to process improvements and best practices. The role involves close coordination with team members across locations, adherence to GMP and company standards, and active participation in meetings and reviews to ensure project timelines and quality objectives are met.
Qualifications
Strong technical foundation in pharmaceutical sciences or a related discipline, with the ability to understand dosage forms, formulation principles, and drug delivery technologies.
Experience working in GMP-regulated environments, with familiarity in documentation practices, quality systems, and compliance expectations.
Proficient in data analysis, problem-solving, and basic statistical interpretation to support experiments, investigations, or project decisions.
Effective communication and collaboration skills to work with multidisciplinary teams and present findings clearly in written and verbal formats.
Ability to manage multiple tasks, prioritize work in a fast-paced setting, and maintain attention to detail and accuracy.
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or a closely related field.
Prior experience in formulation development, product scale-up, or technical operations in the pharmaceutical industry is an advantage.
Comfort working on-site in laboratory or production settings, with a commitment to safety, continuous learning, and professional development.

Work arrangement
No

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