Bachelor’s Degree in Biotechnology, Chemical Engineering, Bioprocess Engineering, Biochemistry or equivalent field.
4 - 11 years of hands-on experience in biopharmaceutical or pharmaceutical Drug Substance manufacturing or related process operations.
Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led global biopharmaceuticals company. Biocon Biologics is engaged in developing high quality, affordable biosimilars that can expand access to a cutting-edge class of therapies to patients globally. It is uniquely positioned as a fully integrated pure play biosimilars organization in the world and aspires to transform patient lives through innovative and inclusive healthcare solutions. The Company has a large portfolio of biosimilars under global clinical development with three of these commercialized in at least one of the developed markets of EU, U.S. and Japan. Biocon Biologics has a product pipeline of 28 molecules, including 11 with Mylan, several with Sandoz and is developing many independently. Biocon Biologics believes that strong partnerships offer enormous opportunities to co-create the future of healthcare, building a patient ecosystem beyond the product, which can transform millions of lives.
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At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run what runs the world.
Leading the ICSS engineering scope across all project phases – FEED, basic engineering, detailed engineering including hardware and software, FAT, pre-commissioning, commissioning and SAT at yards and offshore sites.
Acting as subject matter expert for all automation systems including – DCS, ESD, F&G and co-ordinate with teams both in-house and at the execution center in the region.
Interfacing with vendors, EPC contractors, client, and internal stakeholders to ensure system integration and functional compliance in line with project requirements.
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Ensure technical product compliance with internal ZF specifications, processes, and external requirements (substances, certifications, OE/customer specifications) for conventional shock absorbers.
Execute product engineering tasks according to ZF GD-PEPs for aftermarket, including benchmarking, specification definition, technical design, documentation, sample testing, validation, homologation, and product release (PEDA).
Deliver projects on time, within quality standards, and budget for new product releases and changes to existing products.
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Job Summary Responsible for inspecting products and processes to ensure they meet quality standards and specifications. Key Responsibilities Inspect raw materials, in-process, and finished products Ensure products meet required quality standards and specifications Identify defects and report non-conformance issues Maintain inspection records and quality documentation