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Associate Manager - Project Management (Biologics) 1

6.00 to 9.00 Years   Hyderabad   19 Jul, 2021
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryEducation / Training
Functional AreaSales / BD
EmploymentTypeFull-time

Job Description

Designation: Associate Manager Project ManagementJob Location: BangaloreDepartment: Global Program ManagementAbout 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: This role will support projects in Biologics operational unit at Syngene. This individual will be responsible for ensuring the projects are delivered on time, budget and quality.Key Responsibilities: Responsible for scope setting, developing roadmap, and report building Lead the overall execution of multiple projects, including initiation, budgeting, scheduling, monitoring, and closure according to Good Laboratory Practices, Good Manufacturing Practices, safety, and environmental requirements. Ensure vital communication within the project teams (meetings, minutes, action items) and coordinates / collaborates with other departments and Customer relationship management. To coordinate internal resources, third parties/vendors, and multidisciplinary activities to ensure that the project deliverables are on-time, in-full, and in quantity. Follow up and track all the actions coming from the Project Management Office project meeting while tracking lessons learned. Handle project risks and strategic influencing to maintain project timelines Create and maintain comprehensive project documentation Responsible for weekly and monthly reports by partnering with all the stakeholders to collect and analyze data and structure weekly/monthly reports for final submission. Effectively apply Project Management Institute methodology and enforce project management standards. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety Ensure environment, health, and safety (EHS) measures are imparted via training and adhered within the teamEducational Qualification: Masters in life sciences, with a background in large molecules (Biological) process development and manufacturing like Biosimilars, antibodies, Biotherapeutics, etc., or Master s in Business administration with project management experience in the Biopharma industry. PMP certification or six sigma/Prince 2/ Agile certifications will be an added advantageTechnical/functional Skills: Should be well-versed in Technology transfer, Scale-Up, Manufacturing & outsourcing scenarios of Large molecule manufacturing Must possess full fluency in MS Office (Word, Outlook, PowerPoint) with knowledge of using Microsoft Project (MS Project, Primavera) to monitor, control, and provide overall visibility to the organization. Knowledge of manufacturing (process, equipment, facility, automation) & quality (GLP, cGMP, 21 CFR Part 11 validation, etc.). Good understanding of product development lifecycle. Knowledge of Quality Assurance, CAPA, Change Control, Document Control, Training Systems. Possess the knowledge and exposure to environment, health, and safety (EHS) practices .Experience: At least 6 years of project management experience with a minimum of 9 years of overall experience in Contract research organization or pharmaceutical industry An added advantage with experience in operational excellence/improvement projects focused on standardization, scalability, and robustness in development and manufacturing environments.Behavioral Skills: Excellent in Communication skills (English - both oral and written). Self-directed, proactive, responsive, and able to handle competing priorities with the ability to work independently with minimal direction Ability to focus on a variety of issues and aim to drive results; interact with a variety of stakeholders and foster cross-functional / cultural teamwork Great teammate and strong stakeholder management skills Must be service-minded, flexible, and possess strong interpersonal skills. The ability to handle multiple conflicting tasks in a fast-paced environment is a must.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 :
missalescustomer relationsmanagementproject management officequalityms officestatements of work sow

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