Job Description

JOB DESCRIPTIONDesignation: Research Associate (9-I) or Senior Research Associate (9-II)Job Location: BangaloreDepartment: BBRC PD ARD - GMPAbout SyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene's clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- a strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation.Job Purpose (1-2 Lines): Analytical Research and Development working on Analytical GMP testing (AGT), and Syngene BMS Laboratory (SBL) stability programsKey Responsibilities:

• Analysis of API clinical campaign samples manufactured in Syngene pilot plant
• Qualification or requalification of API reference standards.
• Performing method validation, and method transfers
• Troubleshooting HPLC, dissolution apparatus and other analytical instruments in the lab
• Deliver analytical results within the established windows and as per applicable guidelines
• Compliance & implementation of quality systems
• Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
• Electronic lab notebook documentation
• Miscellaneous lab responsibilities

Educational Qualifications: M.Sc. Chemistry for 9-I; M.Sc. Chemistry or M. Pharm for 9-II;

• The candidate should have a good educational and theoretical, analytical chemistry background
• Good knowledge of analytical techniques
• Good understanding of documentation as per GxP requirements (electronic notebook)
• The candidate should have good proficiency in MS office tools
• Experience in stability samples testing and good knowledge of ICH guidelines & cGMP regulatory requirements
• Must have worked in a cGMP-regulated environment, exposure to regulatory inspections like US FDA, MHRA, etc. is preferred.

Experience: 1-2 years with M.Sc. for 9-I ; 3-5 years with M.Sc. or 1-2 years with M. Pharm for 9-IIBehavioral Skills:

• Strong commitment toward work and a high level of dedication, enthusiasm, and motivation
• Good speaking-listening-writing skills, attention to detail, proactive self-starter
• Ability to work successfully in a dynamic environment
• Should be able to work in a team and flexible for working in shifts.

Equal Opportunity Employer:It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Syngene International