Principal Scientist, QC Micro Job in New Jersey (NJ), Laboratory Career, Full Time Jobs in Novartis Pharmaceuticals
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Principal Scientist, QC Micro job in Morris Plains

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Novartis Pharmaceuticals jobs
New Jersey (NJ), Morris Plains
Job Code:  247443BR
Employer:  Novartis Pharmaceuticals
Category:  Laboratory
Job Type:  Full Time

Location
Country:  United States
State:  New Jersey (NJ)
City:  Morris Plains
Map: 
09/05/2018

Description
Lead, manage and track progress of projects consistent with the priorities. Create and manage Change Controls as applicable. Method Development/Continuous Improvement Lead the development and/or optimization of methods as the needs arise or to replace existing ones. Lead scientific innovation efforts to identify, evaluate and implement novel laboratory technologies Technology transfer Work in conjunction with Quality Control Experts and experts from other applicable functions to evaluate, using a risk-based approach, new and existing methods being transferred to CMOs. Work in conjunction with Quality Control Experts and experts from other applicable functions to perform Quality Risk Assessments and generate other technical documentation including analytical/microbiological development protocols/reports, transfer protocols/reports, validation protocols/reports, trending reports, technical memos, etc. Compliance Ensure that all planned, executed and documented activities are aligned with Quality Manuals/GOPs, company and site policies. Participate in cross-functional teams for development and implementation of quality improvements. Provide training as necessary. Ensure adherence to all company policies and procedures relating to current Good Manufacturing Practices, Standard Operating Procedures and Health, Safety and Environmental Protection regulations. Support of Quality Control and other departmentsBS/MS or equivalent in Chemical or Biochemical engineering, Microbiology, Biotechnology, Biochemistry or other Life Science-related field Fluent in speaking / writing in English •Experience in method development/validation, Quality Control or a technical support function. Minimum: 8-10 years of experience. •Demonstrated knowledge and skills in multiple analyti-cal/microbiological techniques. •Previous project management experience. •Knowledgeable in ISO, ICH and FDA/EMEA/JP cGMP requirements. •Ability to plan, prioritize and execute multiple tasks simultaneously under tight deadlines. •Ability to manage projects and lead teams utilizing modern project management methodology and tools. •Knowledge of statistical tools and methods. •Strong verbal and written technical communication skills. •Strong interpersonal skills. •Proficiency using MS Word, Excel, and MS project.
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