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Job Location | Bangalore |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | Operations Management / Process Analysis |
EmploymentType | Full-time |
Job Title: Downstream MABS Company: Leading BioPharma Company in Bangalore Location Designation: Associate Manager to ManagerReporting to: Head of Downstream No. of Position: 2Division: BiologicsDepartment: Downstream Job Location: BangaloreQualification: M.Tech/ Phd Chemical Engineering / Bioprocess technology/ Biochemical EngineeringYears of Experience: 5 to 10 YearsSalary Range: 25 LPAContact Person:Mr.Zabi MogalMobile: 7676936384 Email ID: zabi@bvrpc.com Job description: The purification team plays a key role in the development of manufacturing processes for biologics. The candidate will be a team lead in the purification team and will be responsible for developing and characterizing purification processes to be scaled - up to the manufacturing facility. This role requires operating in a matrix team environment of process and in - process analytical scientists. The lead will supervise a team working on projects for end to end development, characterization, scale up and validation support. Key Responsibilities:1. Managing & Co-ordination of CMC Downstream for a project. Lead a team of scientists and interns.2. Co- ordination with Senior Management and inter departments ( MSAT, QA & Production group ) for technical updates relative to process development, technology transfer and process improvements. 3. Use DOE approach and past experience to plan experiments for process development, process characterization & process improvement of DSP Operations (Chromatography & filtration).4. Identify gaps and scope of improvement in the process, workflow; improvements for COGs reduction; Formalize the strategy for advancements.5. Technical & functional risk analysis and mitigation.6. Assimilate data from multiple sources and projects to analyze the outcome of experiments.7. Comparative data evaluation with manufacturing scale batches to define ranges and specifications.8. Review of critical technical documents supporting regulatory submissions.9. Identification of intection with external consultants for technical and regulatory advisories.Qualification:Education & Experience:M.Tech/Phd Chemical Engineering, Bioprocess technology, Biochemical Engineering with 5 to 10 Years of Experience in process Development, process characterization and/or scale up of purification processes for biologics.Technical & soft skills requirements:1. Comprehensive knowledge of Chromatography and filtration theory and techniques and protein chemistry.2. Strong communication, Inter- personal, presentation, technical authoring and motivational skills.3. End to End knowledge in CMC Development.4. Expertise in DOE and analytical techniques. Salary: Not Disclosed by Recruiter Industry: Pharma / Biotech / Clinical Research Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology Role Category: R&D Role: Bio-Technical Research Associate/Scientist Employment Type: Full Time, Permanent, Education:UG -B.Tech/B.E. - Bio-Chemistry/Bio-Technology, Biomedical, ChemicalPG - M.Tech - Chemical, Bio-Chemistry/Bio-Technology, BiomedicalDoctorate - Ph.D - Advertising/Mass Communication
Keyskills :
continuous improvement facilitationsoft skillsrisk analysispilot projectssenior managementprocess improvementtechnology transferprocess developmentchemical engineeringmanufacturing processes