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Associate MSAT

3.00 to 9.00 Years   Delhi   22 Nov, 2022
PFIZER LIMITED
Job LocationDelhi
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    As an Associate Scientist, you will be at the center of our operations and youll find that everything we do, every day, is in line with an unwavering commitment to quality. You will perform qualitative and quantitative analyses of organic, inorganic compounds, or biologics. This will help you determine chemical and physical properties during chemical syntheses, fermentation or drug product development process by verifying their identity, purity, and homogeneity.Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItExercise and build basic team effectiveness skills {e.g., commitment, feedback, consensus management) within the work group.Prepare and review technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.Direct interaction with project team members, including presentation of data.Complete all Good Laboratory Practice {part of GxP}and safety training in compliance with departmental requirements and follow appropriate safety practices in the workplace.Work closely with process experts and project teams to provide timely support for formulators in the form of quality data which can be used in support of regulatory documentation of new drug applications.Independently carry out all aspects of practical work necessary to provide right first time results.Responsible for performing feasibility studies, MOC studies, dwell time studies and lab scale batches as part of technology transfer activities.Responsible for performing Engineering batches, scaleup batches, and Exhibit batches as part of technology transfer activities.Attend project team and brainstorming meetings and present data.Responsible for providing the required data for regulatory submissions.QualificationsMust-HaveBachelors DegreeExperience with Quality Systems in a Good Manufacturing Practices {also cGMP} environmentExperience with technology transfer activities or formulation development of Sterile injectables.Ability to extract relevant information from scientific literature, and accurately record observations, facts, data, and conclusions during studies or Good Manufacturing Practices {also cGMP} investigationsInteract effectively with peers and leaders as part of a multi-disciplinary teamEffective verbal and written communication skillsNice-to-HaveHands on experience with protein purificationWorking knowledge and ability to operate analytical and physical techniques used for the characterization of pharmaceutical substances and productsGood understanding in extractable and leachable method validations,

Keyskills :
Manufacturingprotein purification

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