Blue Jet Healthcare Ltd
Website:
bluejethealthcare.com
Job details:
Company Description Blue Jet Healthcare Ltd is a science-driven CDMO and specialty pharmaceutical ingredients company with over five decades of experience partnering with global pharmaceutical and healthcare organizations. The company supports both innovator and generic pharmaceutical firms in taking molecules from laboratory development to commercial-scale manufacturing through deep process chemistry expertise, strong engineering capabilities, and a proven record of reliable supply. Its integrated CDMO platform spans process development, scale-up, technology transfer, advanced manufacturing, and long-term supply partnerships, delivering scalable and regulatory-aligned solutions worldwide. Blue Jet Healthcare operates three modern manufacturing facilities in Maharashtra, India, with significant installed capacity, and is expanding with a greenfield facility in Andhra Pradesh.. Key business segments include contrast media intermediates, artificial sweeteners, pharmaceutical intermediates and APIs, and protected amino acids and derivatives for complex and emerging therapies.
Role Description The Assistant Manager role is a full-time, on-site position based in New Green field project site located at Rambilli Industrial Park Phase II, Atchutapuram. The Assistant Manager will support plant or functional operations through planning, coordinating, and monitoring daily activities to meet production, quality, safety, and compliance targets. Responsibilities typically include supervising team members, tracking performance metrics, preparing reports, and implementing process improvements in line with company standards and regulatory requirements. The role will involve close collaboration with cross-functional teams such as production, quality assurance, maintenance, supply chain, and EHS to ensure smooth operations and adherence to SOPs. The Assistant Manager is expected to maintain accurate documentation, support audits, assist in training team members, and escalate issues promptly to leadership while contributing to a culture of continuous improvement and operational excellence.
Qualifications
- Strong operational management and supervisory skills, including team coordination, workload planning, and performance monitoring.
- Experience in pharmaceutical or chemical manufacturing environments, with familiarity in CDMO operations, process chemistry, or specialty ingredients.
- Solid understanding of quality systems, GMP or relevant regulatory requirements, and audit/readiness processes.
- Proficiency in data analysis, reporting, and use of MS Office or similar tools to track KPIs and operational performance.
- Effective communication and interpersonal skills for working with cross-functional teams and external stakeholders.
- Proven ability to identify process issues, implement improvements, and support change management initiatives.
- Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related scientific or technical discipline; a relevant postgraduate qualification is an advantage.
- Demonstrated ability to work on-site in an industrial setting, with commitment to safety, environmental, and compliance standards.
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