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| Job Location | Pune |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Operations Management / Process Analysis |
| EmploymentType | Full-time |
Designation: Senior ExecutiveJob Location: BangaloreDepartment: Quality Assurance - GLPAbout Syngene Incorporated 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 around the world. 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- 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: To Ensure the compliance to Organization for Economic Co-Operation and Development (OECD) principles of Good Laboratory Practices (GLP), Good Clinical Laboratory Practices (GCLP) and ICH GCP. Key Responsibilities: Receipt and review of general documents/SOPs, MOA, Study Plans and Study Reports. Preparation and /or review of SOPs and other documents related to QAU. Maintain copies of approved Study Plans, MOA and general documents. Review of Method of Analysis and Study plan. Performing/scheduling study, facility and process based inspections. Perform audit of study raw data & study report. Report the observations/findings of inspections to the respective auditee and management in a timely manner. Review of electronic data and audit trail for data generated in bioanalysis. Review of computerized system documents with respect to OECD 17,21 CFR Part 11 and GAMP. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted company.Educational Qualification: Master of Science in Microbiology / BiotechnologyTechnical/functional Skills: Should be well versed with OECD GLP Principles, Bioanalytical Method development and Validation Guidance (Such as USFDA, EMEA, ANVISA), GCLP Guidance, ICH-GCP Guidance. Well versed in electronic data audit. Good Knowledge on handling the application softwareExperience: 3-6 Years Experience.Behavioral Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should able to work in team and flexible for working in shifts. Should be a focused employee.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.,
Keyskills :
audit trailcustomer relationscontinuous improvement facilitationsalesdeliverymismethod developmentcustomer serviceequal employment opportunityanimal health21 cfrconsumer goodscommitment towards work