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Senior Scientist Formulations Development

4.00 to 6.00 Years   Chennai   10 Jul, 2021
Job LocationChennai
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

Senior Scientist, Formulations DevelopmentROLE SUMMARYThe Senior Scientist position is a laboratory-based position responsible for formulation development, investigating early stage conceptualization of injectable dosage form. This position requires exceptional time management and communications skills with a strong attention to detail. A breadth of knowledge of analytical tools and techniques applied to injectable formulation science, stability, process development and tech transfer approaches for formulation design is required. To provide necessary documentation for regulatory submissions as required including deficiency responses. To train on novel technical expertise required for scientist including electronic documentation, Sterility assurance of Injections and pertinent Intellectual property.ROLE RESPONSIBILITIES

  • Design and execution of pharmaceutical development experiments
  • Ability to work in fast paced, multidisciplinary project teams, and collaborate with colleagues to define and implement screening and characterization strategies according to project timelines
  • Applies technical expertise to develop solutions to a wide range of problems of varying complexity, may refer to precedents and policies
  • Ability to gather, analyze, apply, and interpret information and identify cause and effect relationships
  • Contributes to the completion of specific programs and projects. Ensures that projects are completed on schedule following established procedures and schedules
  • Collect and share relevant academic literature, leverage external consultants/SMEs, and establish new collaborations with internal groups
  • Review and verify scientific experiments and data documented in electronic laboratory notebooks and technical reports
BASIC QUALIFICATIONS
  • MS or M Pharm in Pharmaceutics
  • 4-6 years of experience in sterile formulation and process development
  • Ability to perform laboratory studies, analyze and interpret data from a variety of sources.
  • Strong aptitude for learning process technology and equipment
  • Excellent written and oral communication skills
  • Demonstrated ability to interact effectively with all levels of the organization including diverse educational and cultural backgrounds.
  • Flexibility and ability to embrace and lead chance
  • Ability to work in a high-paced team environment
PREFERRED QUALIFICATIONS
  • PhD in Pharmaceutical Sciences
  • Experience in sterile injectables R & D
  • Experience in a cGMP sterile environment including specific knowledge of and experience with Sterile Drug Product processing and equipment
  • Six Sigma Basic certification
PHYSICAL/MENTAL REQUIREMENTS
  • Preferably good in numerical ability
  • Standing to conduct experiments, Observing and online documenting
  • Able to work in oncology lab with all necessary PPEs
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
  • Occasionally to work on shifts
  • No objection with PPEs while working in oncology lab
ORGANIZATIONAL RELATIONSHIPS
  • Design, execution of Pharmaceutical product development trials and establish procedures for Injectable product evaluation
  • Review experiments conducted at external labs, data analysis and interpretation
  • To be involved in small group discussions and responsible for data analysis and interpretation
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Research and Development #LI-PFE,

Keyskills :
researchvalidationdocumentationapihplcresearchdevelopmentequal employment opportunitysmall groupdata analysistech transferproject teamstime managementgroup discussionsoral communication

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