USP looking for Associate Scientific Liaison | M.Sc, Ph.D

 

 

USP is proud to be an equal opportunity/affirmative action employer. Employment selection and related decisions are made without regard to sex, gender identity, race, age, disability, religion, national origin, color, veteran status or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Post : Associate Scientific Liaison

Job Description

  • Develops new monographs and revises existing monographs based on supporting data submitted by USP global laboratories and external sponsors
  • Evaluates analytical methodology and acceptance criteria
  • Redesigns existing official monographs
  • Works closely with a team of high‐performing scientists responsible for the development and revision ofdocumentary standards
  • Works with USP staff, regulatory agencies, stakeholders, and other pharmacopeias as related to monograph development
  • Provides information to the relevant USP Expert Committee(s) in support of monograph development
  • Serves as a mentor for other staff and leads training efforts, as needed
  • Serves as a member on USP cross‐functional teams, as needed
  • Prepares manuscripts for publication by USP (e.g. stimuli articles) or in peer‐reviewed journals
  • Represents USP at scientific conferences/meetings, outreach visits and other events sponsored by USP, the pharmaceutical industry, trade organizations and regulatory agencies
  • Participates in the development and/or review of USP’s professional education course materials and may serve as an instructor, as needed
  • Collaborates closely with Compendial Development Laboratories, Reference Standards Evaluation, Reference
  • Standards Laboratories, Publications, Executive Secretariat, Compendial Affairs and other departments on monograph‐related issues
  • Tracks and reports frequently to management on the status of assignments
  • Performs other duties as assigned

Candidate Profile
• Ph.D. in Chemistry, Biochemistry or allied field with a minimum of 5 years, or M.Sc. and 7 years of relevant
• experience with USP‐NF tests and standards
• Minimum of 5 years of experience with analytical techniques such as chromatography, wet chemistry,
• spectroscopy, titration, etc.
• Knowledge of compendial standards related to pharmaceutical industry
• Knowledge of regulatory requirements and guidelines for pharmaceuticals (e.g. FDA, ICH, etc.)
• An equivalent combination of experience and education may be substituted
• Able to establish and nurture relationships with individuals of varying backgrounds and learning styles
• Able to operate independently where appropriate, yet understands when to escalate issues and how to
• establish effective working relationships
• Strong presentation and communication skills (written and oral)
• Well‐developed organizational, interpersonal communications, negotiation, writing, and strong listening skills
• Knowledge of internet and electronic database searches helpful
• Practical experience in scientific, analytical techniques
• Project Management skills required
• Knowledge of the pharmaceutical industry and the associated regulatory framework is essential
• Ability to prioritize tasks and manage multiple projects simultaneously
• Must be able to share technical information with non‐technical or non‐scientific staff, and to communicate effectively with representatives from pharmaceutical companies, government, and academic institutions.

Additional Information
Experience : 5 years
Qualification : M.Sc, Ph.D
Location :
Hyderabad, Andhra Pradesh
Industry Type : Pharma/ Healthcare/ Clinical research
Tracking Code : 1418-679
Functional Area : Scientific Liaison
End Date : 5th June, 2019

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