Complies with Quality Principals related to data generation and reporting and adjusts Quality Systems to match the project stage (e.g. Work is expected to result in the development of new or refined products, processes or equipment, Selects techniques to solve complex problems and make sound design recommendations, Release and stability testing at internal and external laboratories, Write CMC sections to support IDE and PMA submissions for combination products, Participate in cross-functional product development teams and provide technical support to sterilization process selection, packaging specification requirements, clinical manufacturing, quality assurance, analytical R&D, and regulatory affairs, The selected candidate must have an ability to collaborate effectively with other scientists in a multidisciplinary team environment and possess excellent verbal and written communication skills, PhD in Pharmaceutical Sciences (Pharmaceutics), Chemistry (Physical, Organic, or Analytical), Biomedical Engineering or related technical field, 1-3 years of industry experience in pharmaceuticals under a research and development environment, Understanding and experience in pre-clinical model development, Previous experience with major analytical techniques such as HPLC, GC, LC/MS, GC/MS, and NMR, Experience in practical lab-based Pharmacokinetics/Pharmacodynamics data analysis, Good understanding of cell biology, pharmacology, and biochemistry is highly desirable, Good understanding of controlled drug delivery systems, Deep understanding of pharmaceutics and physical chemistry is a must, Substantial knowledge in assay method development and validation and familiarity with release and stability testing are desirable, Responsible for running all monthly pharmaceutical procurement reports and serve as primary point of contact for questions related to these monthly reports, Maintain all electronic product catalogs with national drug distributors that link to FMS Pharmaceutical Formulary, Update and maintain all catalogs to ensure accurate pricing in all systems, Update all systems including SAP to ensure that FMS facilities have access to purchase the most cost effective Formulary products that are linked to contracted pharmaceutical suppliers, Support Corporate Medical and Clinical Services departments to drive FMS clinics compliance to the FMS drug formulary, Assist Pharma Procurement leaders in review of all available direct and Group Purchasing Contracts to determine the best pricing available by generic drug class for any multi source medications listed on FMS Pharmaceutical Formulary, Conduct daily oversight of the daily SAP Pharma distributor interface, Assist FMS Corporate and Division Finance Centers in resolving any problems encountered with the interface. Ensure proper qualification, validation, and maintenance of all equipment, Provide professional development opportunities for all personnel. Showing strong talent to negotiate, to influence and to listen carefully. H1-B status) now or in the future.Administration, Prepare concise and well-written reports, memos, proposals, and white papers, Maintain security and confidentiality of all protected health information encountered during performance and other essential functions, Lead meetings, team projects, training on hot topics in the industry, and discuss current topics with clients and inter-professional team, Collaborate with and understand a wide variety of healthcare professionals, including but not limited to: pharmacists, pharmacy technicians, pharmacy students, other healthcare professionals, educators, and payer drug coverage decision makers, Articulate and know where to access the drug-pricing spectrum—including but not limited to a variety of drug pricing schemes, both on the manufacturer, wholesaler, as well as payer sides of pharmacy. Writes complex explicit documentation for new procedures, as well as for current procedures, Supports the qualification and startup of new equipment in the Fill and Finish area, Develops training manuals and / or on-the-job training materials for new and existing equipment and processes in assigned department. When appropriate, leads organizational objectives and delegates responsibilities. Explore pharma production Jobs openings in India Now. answer questions, assist employees, etc. investigations / deviations, CAPAs, change controls, etc. An individual contributor will have significant project/process responsibilities, Follows processes and operational policies in selecting methods and techniques for obtaining solutions. Championed quality initiatives. Play a key role in the formulation of formulations strategies and tactics, Lead the formulations team effort in the transfer efforts, to include creating a transfer plan, related timelines and metrics for measuring progress, Provide technical support to resolve QC and production technical issues, Prepare complex solutions, such as buffers, antigen conjugate solution, antibody conjugate solution, gold-antibody conjugate solution, Optimize formulations and performance of gold-antibody conjugate pad, Conduct complex experimentation including data collection, summary and thorough analysis, in support of product improvement and validation projects. Use these resumes as templates to get help creating the best Production Supervisor resume. Provide technical leadership skill in all activities related to the development of the assigned engineering projects, Industrial experience preferably 10+ years, Successfully demonstrated several years (mini-mum of 3 years) of directly related experience (within relevant industrial setting), Meet quality, quantity and timelines in all assigned projects, Plan, organize, perform and document scientific experiments/plant activities in collaboration with experienced team members if necessary. Report progress and results to Supervisor on a regular basis, Establish and maintain lines of communication to ensure the timely and accurate flow of information. Partner with organization (Sales / BDMs) to ensure development of programs, tools initiatives to improve performance. Involved in management of all program phases including sourcing, contract negotiation, planning, and final bill completion, while maintaining high level of data integrity and timeliness, 20% STRATEGIC LEADERSHIP AND RELATIONSHIP MANAGEMENT: Be a trusted advisor to client stakeholders across multiple business units; Develops overall congress plans/strategy and budgets for congress stakeholders; Creates best practices based on industry benchmarking and knowledge; Develops and reports on program metrics; Analyzes operational data to identify cost savings, operational efficiencies and advises on ways to maximize ROI, OTHER: May require travel to destinations worldwide, in support of client site inspections and/or program operations. take ownership of training records for self-development and submit to supervision in timely manner, training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc. In assigned projects, networks and/or platforms 's degree and resume for pharma production years pharmaceutical testing experience file management solutions! 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